PALATIN TECHNOLOGIES INC
10-Ks and 10-Qs
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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 10 - Q
☑
QUARTERLY
REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE
ACT OF 1934
For the
quarterly period ended September 30, 2018
or
☐
TRANSITION
REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE
ACT OF 1934
For the
transition period from ___________ to __________
Commission
file number: 001-15543
PALATIN TECHNOLOGIES, INC.
(Exact
name of registrant as specified in its charter)
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Delaware
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95-4078884
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(State
or other jurisdiction of
incorporation
or organization)
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(I.R.S.
Employer Identification No.)
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4B Cedar Brook Drive
Cranbury, New Jersey
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08512
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(Address
of principal executive offices)
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(Zip
Code)
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(609) 495-2200
(Registrant’s
telephone number, including area code)
Indicate
by check mark whether the registrant (1) has filed all reports
required to be filed by Section 13 or 15(d) of the Securities
Exchange Act of 1934, as amended during the preceding 12 months (or
for such shorter period that the registrant was required to file
such reports), and (2) has been subject to such filing requirements
for the past 90 days.
Yes
☑ No ☐
Indicate
by check mark whether the registrant has submitted electronically,
every Interactive Data File required to be submitted pursuant to
Rule 405 of Regulation S-T
(§232.405 of this chapter)
during the preceding 12
months (or for such shorter period that the registrant was required
to submit such files).
Yes ☑ No ☐
Indicate
by check mark whether the registrant is a large accelerated filer,
an accelerated filer, a non-accelerated filer, a smaller reporting
company, or an emerging growth company. See the definitions of
“large accelerated filer,” “accelerated
filer,” “smaller reporting company,” and
“emerging growth company” in Rule 12b-2 of the Exchange
Act:
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Large accelerated filer
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☐
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Accelerated filer
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☑
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Non-accelerated
filer
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☐
(Do not check if a smaller reporting
company)
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Smaller reporting company
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☑
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Emerging
growth company
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☐
|
If an
emerging growth company, indicate by check mark if the registrant
has elected not to use the extended transition period for complying
with any new or revised financial accounting standards provided
pursuant to Section 13(a) of the Exchange Act.
☐
Indicate
by check mark whether the registrant is a shell company (as defined
in Rule 12b-2 of the Exchange Act). Yes ☐ No
☑
Indicate
the number of shares outstanding of each of the registrant’s
classes of common stock, as of the latest practicable date
(November 8, 2018): 203,063,429.
PALATIN TECHNOLOGIES, INC
.
Table of Contents
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Page
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PART I – FINANCIAL INFORMATION
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Item 1. Financial Statements (Unaudited)
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Consolidated
Balance Sheets as of September 30, 2018 and June 30,
2018
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5
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Consolidated
Statements of Operations for the Three Months Ended September 30,
2018 and 2017
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6
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Consolidated
Statements of Comprehensive (Loss) Income for the Three Months
Ended
September 30, 2018
and 2017
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7
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Consolidated
Statements of Stockholders’ Equity for the Three Months Ended
September 30, 2018 and 2017
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8
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Consolidated
Statements of Cash Flows for the Three Months Ended September 30,
2018 and 2017
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9
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Notes
to Consolidated Financial Statements
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10
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Item 2. Management’s Discussion and Analysis of Financial
Condition and Results of Operations
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24
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Item 3. Quantitative and Qualitative Disclosures About Market
Risk
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28
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Item 4. Controls and Procedures
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28
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PART
II – OTHER INFORMATION
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Item 1. Legal Proceedings
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29
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Item 1A. Risk Factors
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29
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Item 2. Unregistered Sales of Equity Securities and Use of
Proceeds
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29
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Item 3. Defaults Upon Senior Securities
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29
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Item 4. Mine Safety Disclosures
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29
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Item 5. Other Information
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29
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Item 6. Exhibits
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30
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Signatures
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31
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Special Note Regarding Forward-Looking Statements
In this
Quarterly Report on Form 10-Q, references to “we,”
“our,” “us,” the “Company” or
“Palatin” means Palatin Technologies, Inc. and its
subsidiary.
Statements
in this Quarterly Report on Form 10-Q, as well as oral statements
that may be made by us or by our officers, directors, or employees
acting on our behalf, that are not historical facts constitute
“forward-looking statements,” which are made pursuant
to the safe harbor provisions of Section 21E of the Securities
Exchange Act of 1934 (the “Exchange Act”). The
forward-looking statements in this Quarterly Report on Form 10-Q do
not constitute guarantees of future performance. Investors are
cautioned that statements that are not strictly historical facts
contained in this Quarterly Report on Form 10-Q, including, without
limitation, the following are forward looking
statements:
●
estimates of our
expenses, future revenue and capital requirements;
●
our ability to
achieve and maintain profitability;
●
our ability to
obtain additional financing on terms acceptable to us, or at
all;
●
our ability to
advance product candidates into, and successfully complete,
clinical trials;
●
the initiation,
timing, progress and results of future preclinical studies and
clinical trials, and our research and development
programs;
●
the timing or
likelihood of regulatory filings and approvals;
●
our expectations
regarding completion of required clinical trials and studies and
validation of methods and controls used to manufacture
Vyleesi™ (the trade name for bremelanotide) for the treatment
of premenopausal women with hypoactive sexual desire disorder
(“HSDD”), which is a type of female sexual dysfunction
(“FSD”);
●
our expectation
regarding the timing of our regulatory submissions for approval of
Vyleesi for HSDD in the United States and in certain other
jurisdictions outside the United States;
●
our expectation
regarding performance of our exclusive licensees of Vyleesi,
including;
o
AMAG
Pharmaceuticals, Inc. (“AMAG”) for North
America,
o
Shanghai Fosun
Pharmaceutical Industrial Development Co. Ltd.
(“Fosun”), a subsidiary of Shanghai Fosun
Pharmaceutical (Group) Co., Ltd., for the territories of the
People’s Republic of China, Taiwan, Hong Kong S.A.R. and
Macau S.A.R. (collectively, the “Chinese Territories”),
and
o
Kwangdong
Pharmaceutical Co., Ltd. (“Kwangdong”) for the Republic
of Korea (“Korea”);
●
the potential for
commercialization of Vyleesi for HSDD in North America by AMAG and
other product candidates, if approved, by us;
●
our expectations
regarding the potential market size and market acceptance for
Vyleesi for HSDD and our other product candidates, if approved for
commercial use;
●
our ability to
compete with other products and technologies similar to our product
candidates;
●
the ability of our
third-party collaborators to timely carry out their duties under
their agreements with us;
●
the ability of our
contract manufacturers to perform their manufacturing activities
for us in compliance with applicable regulations;
●
our ability to
recognize the potential value of our licensing arrangements with
third parties;
●
the potential to
achieve revenues from the sale of our product
candidates;
●
our ability to
obtain adequate reimbursement from Medicare, Medicaid, private
insurers and other healthcare payers;
●
our ability to
maintain product liability insurance at a reasonable cost or in
sufficient amounts, if at all;
●
the performance of
our management team, senior staff professionals, and third-party
contractors and consultants;
●
the retention of
key management, employees and third-party contractors;
●
the scope of
protection we are able to establish and maintain for intellectual
property rights covering our product candidates and technology in
the United States and throughout the world;
●
our compliance with
federal and state laws and regulations;
3
●
the timing and
costs associated with obtaining regulatory approval for our product
candidates;
●
the impact of
fluctuations in foreign exchange rates;
●
the impact of
legislative or regulatory healthcare reforms in the United
States;
●
our ability to
adapt to changes in global economic conditions as well as competing
products and technologies; and
●
our ability to
remain listed on the NYSE American stock exchange.
Such
forward-looking statements involve risks, uncertainties and other
factors that could cause our actual results to be materially
different from historical results or from any results expressed or
implied by such forward-looking statements. Our future operating
results are subject to risks and uncertainties and are dependent
upon many factors, including, without limitation, the risks
identified under Part II, Item IA “Risk Factors” and
elsewhere in this Quarterly Report, our Annual Report on Form 10-K
for the year ended June 30, 2018 and in our other reports filed
with the U.S. Securities and Exchange Commission (the
“SEC”). Except as required by law, we do not intend,
and undertake no obligation, to publicly update forward-looking
statements to reflect events or circumstances after the date of
this document or to reflect the occurrence of unanticipated
events.
Palatin
Technologies® is a registered trademark of Palatin
Technologies, Inc. Vyleesi™ is a trademark of AMAG
Pharmaceuticals, Inc. in North America and of Palatin Technologies,
Inc. elsewhere in the world.
4
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PALATIN TECHNOLOGIES, INC
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and
Subsidiary
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(unaudited)
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September
30,
2018
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June
30,
2018
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ASSETS
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Current
assets:
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Cash and cash
equivalents
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$
32,619,064
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$
38,000,171
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Accounts
receivable
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104,189
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-
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Prepaid expenses
and other current assets
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420,639
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513,688
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Total current
assets
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33,143,892
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38,513,859
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Property and
equipment, net
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149,990
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164,035
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Other
assets
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338,916
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338,916
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Total
assets
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$
33,632,798
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$
39,016,810
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LIABILITIES
AND STOCKHOLDERS’ EQUITY
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Current
liabilities:
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Accounts
payable
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$
1,165,151
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$
2,223,693
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Accrued
expenses
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2,020,333
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2,103,021
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Notes payable, net
of discount
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4,305,242
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5,948,763
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Other current
liabilities
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969,179
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487,488
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Total current
liabilities
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8,459,905
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10,762,965
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Notes payable, net
of discount
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-
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332,898
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Deferred
revenue
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-
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500,000
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Other non-current
liabilities
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-
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456,038
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Total
liabilities
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8,459,905
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12,051,901
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Stockholders’
equity:
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Preferred stock of
$0.01 par value – authorized 10,000,000 shares:
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Series A
Convertible: issued and outstanding 4,030 shares as of September
30, 2018 and June 30, 2018
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40
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40
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Common stock of
$0.01 par value – authorized 300,000,000 shares:
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issued and
outstanding 203,032,129 shares as of September 30, 2018 and
200,554,205 shares as of June 30, 2018
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2,030,321
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2,005,542
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Additional paid-in
capital
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360,370,494
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357,005,233
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Accumulated
deficit
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(337,227,962
)
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(332,045,906
)
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Total
stockholders’ equity
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25,172,893
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26,964,909
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Total liabilities
and stockholders’ equity
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$
33,632,798
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$
39,016,810
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The
accompanying notes are an integral part of these consolidated
financial statements.
5
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PALATIN
TECHNOLOGIES, INC.
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and
Subsidiary
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(unaudited)
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Three Months
Ended September 30,
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2018
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2017
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REVENUES:
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License and
contract
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$
34,505
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$
26,941,508
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OPERATING
EXPENSES:
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Research and
development
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3,622,691
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14,163,097
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General and
administrative
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2,040,582
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1,544,575
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Total operating
expenses
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5,663,273
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15,707,672
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(Loss) income from
operations
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(5,628,768
)
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11,233,836
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OTHER INCOME
(EXPENSE):
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Investment
income
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153,583
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51,726
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Interest
expense
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(206,871
)
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(456,677
)
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Total other
expense, net
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(53,288
)
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(404,951
)
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(Loss) income
before income taxes
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(5,682,056
)
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10,828,885
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Income tax
expense
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-
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(225,255
)
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NET (LOSS)
INCOME
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$
(5,682,056
)
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$
10,603,630
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Basic net (loss)
income per common share
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$
(0.03
)
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$
0.05
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Diluted net (loss)
income per common share
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$
(0.03
)
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$
0.05
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Weighted average
number of common shares outstanding used in computing basic net
(loss) income per common share
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205,009,278
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197,112,400
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Weighted average
number of common shares outstanding used in computing diluted net
(loss) income per common share
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205,009,278
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201,360,736
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The
accompanying notes are an integral part of these consolidated
financial statements.
6
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PALATIN
TECHNOLOGIES, INC.
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and
Subsidiary
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Consolidated
Statements of Comprehensive (Loss) Income
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(unaudited)
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Three Months
Ended September 30,
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2018
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2017
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Net (loss)
income
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$
(5,682,056
)
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$
10,603,630
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Other comprehensive
income :
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Unrealized gain on
available-for-sale investments
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-
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437
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Total comprehensive
(loss) income
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$
(5,682,056
)
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$
10,604,067
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The
accompanying notes are an integral part of these consolidated
financial statements.
7
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PALATIN TECHNOLOGIES, INC.
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and Subsidiary
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Consolidated Statements of Stockholders’ Equity
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Preferred
Stock
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Common
Stock
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Shares
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Amount
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Shares
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Amount
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Additional
Paid-in
Capital
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Accumulated
Other
Comprehensive
Income
(Loss)
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Accumulated
Deficit
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Total
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Balance, June 30,
2018
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4,030
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$
40
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200,554,205
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$
2,005,542
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$
357,005,233
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$
-
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$
(332,045,906
)
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$
26,964,909
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Cumulative effect of accounting
change
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-
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-
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-
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-
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-
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-
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500,000
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500,000
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Stock-based
compensation
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-
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-
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319,817
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3,198
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1,230,387
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-
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-
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1,233,585
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Sale of common stock , net of
costs
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-
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-
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2,225,145
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22,251
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2,200,196
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-
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-
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2,222,447
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Withholding taxes related to
restricted stock units
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-
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-
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(67,038
)
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(670
)
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(65,322
)
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-
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-
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(65,992
)
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Net loss
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-
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-
|
-
|
-
|
-
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-
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(5,682,056
)
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(5,682,056
)
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Balance, September 30,
2018
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4,030
|
$
40
|
203,032,129
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$
2,030,321
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$
360,370,494
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$
-
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$
(337,227,962
)
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$
25,172,893
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Preferred
Stock
|
Common
Stock
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Shares
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Amount
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Shares
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Amount
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Additional
Paid-in
Capital
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Accumulated
Other
Comprehensive
Income
(Loss)
|
Accumulated
Deficit |
Total
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Balance, June 30,
2017
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4,030
|
$
40
|
160,515,361
|
$
1,605,153
|
$
349,974,538
|
$
(590
)
|
$
(356,743,785
)
|
$
(5,164,644
)
|
|
Cumulative effect of accounting
change
|
-
|
-
|
-
|
-
|
4,835
|
-
|
(4,835
)
|
-
|
|
Stock-based
compensation
|
-
|
-
|
75,071
|
751
|
421,120
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-
|
-
|
421,871
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Warrant
exercises
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-
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-
|
23,802,575
|
238,026
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(123,642
)
|
-
|
-
|
114,384
|
|
Unrealized gains on
investments
|
-
|
-#
|
-
|
-
|
-
|
437
|
-
|
437
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|
Net income
|
-
|
-
|
-
|
-
|
-
|
-
|
10,603,630
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10,603,630
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|
Balance, September 30,
2017
|
4,030
|
$
40
|
184,393,007
|
$
1,843,930
|
$
350,276,851
|
$
(153
)
|
$
(346,144,990
)
|
$
5,975,678
|
The
accompanying notes are an integral part of these consolidated
financial statements.
8
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PALATIN
TECHNOLOGIES, INC.
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and
Subsidiary
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(unaudited)
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Three Months
Ended September 30,
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2018
|
2017
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CASH FLOWS FROM
OPERATING ACTIVITIES:
|
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Net
(loss) income
|
$
(5,682,056
)
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$
10,603,630
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|
Adjustments
to reconcile net (loss) income to net cash
|
|
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(used
in) provided by operating activities:
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Depreciation and
amortization
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14,045
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14,616
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Non-cash interest
expense
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23,581
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56,182
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Stock-based
compensation
|
1,233,585
|
421,871
|
|
Changes in
operating assets and liabilities:
|
|
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Accounts
receivable
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(104,189
)
|
5,727,100
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Prepaid expenses
and other assets
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93,049
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71,236
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Accounts
payable
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(1,058,542
)
|
482,271
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Accrued
expenses
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(82,688
)
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(1,112,295
)
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Deferred
revenue
|
-
|
(14,890,191
)
|
|
Other non-current
liabilities
|
25,653
|
60,435
|
|
Net cash (used in)
provided by operating activities
|
(5,537,562
)
|
1,434,855
|
|
|
|
|
|
CASH FLOWS FROM
INVESTING ACTIVITIES:
|
|
|
|
Purchases of
property and equipment
|
-
|
(9,500
)
|
|
Net cash used in
investing activities
|
-
|
(9,500
)
|
|
|
|
|
|
CASH FLOWS FROM
FINANCING ACTIVITIES:
|
|
|
|
Payments on capital
lease obligations
|
-
|
(7,110
)
|
|
Payment of
withholding taxes related to restricted
|
|
|
|
stock
units
|
(65,992
)
|
(24,380
)
|
|
Payment on notes
payable obligations
|
(2,000,000
)
|
(2,000,000
)
|
|
Proceeds from the
exercise of common stock warrants
|
-
|
114,384
|
|
Proceeds from the
sale of common stock,
|
|
|
|
net of
costs
|
2,222,447
|
-
|
|
Net cash provided
by (used in) financing activities
|
156,455
|
(1,917,106
)
|
|
|
|
|
|
NET DECREASE IN
CASH AND CASH EQUIVALENTS
|
(5,381,107
)
|
(491,751
)
|
|
|
|
|
|
CASH AND CASH
EQUIVALENTS, beginning of period
|
38,000,171
|
40,200,324
|
|
|
|
|
|
CASH AND CASH
EQUIVALENTS, end of period
|
$
32,619,064
|
$
39,708,573
|
|
|
|
|
|
SUPPLEMENTAL CASH
FLOW INFORMATION:
|
|
|
|
Cash paid for
interest
|
$
157,636
|
$
340,365
|
|
Cash paid for
income taxes
|
-
|
500,000
|
The
accompanying notes are an integral part of these consolidated
financial statements.
9
PALATIN TECHNOLOGIES, INC.
and Subsidiary
Notes to Consolidated Financial Statements
(unaudited)
(1)
ORGANIZATION
Nature of Business
- Palatin Technologies, Inc.
(“Palatin” or the “Company”) is a
specialized biopharmaceutical company developing first-in-class
medicines based on molecules that modulate the activity of the
melanocortin and natriuretic peptide receptor systems.
Palatin’s product candidates are targeted, receptor-specific
therapeutics for the treatment of diseases with significant unmet
medical need and commercial potential. The most advanced product
candidate is Vyleesi™, the trade name for bremelanotide, a
peptide melanocortin receptor 4 (“MC4r”) agonist, for
the treatment of premenopausal women with acquired, generalized
hypoactive sexual desire disorder (“HSDD”), which is a
type of female sexual dysfunction (“FSD”), defined as
low desire with associated distress or interpersonal
difficulty.
A New
Drug Application (“NDA”) has been submitted to the U.S.
Food and Drug Administration (“FDA”) for Vyleesi by our
exclusive North American licensee, AMAG Pharmaceuticals, Inc.
(“AMAG”), and accepted for filing by the FDA, with an
FDA decision on approval expected in the first quarter of calendar
year 2019. Palatin has also licensed rights to Vyleesi to Shanghai
Fosun Pharmaceutical Industrial Development Co. Ltd.
(“Fosun”) for the territories of the People’s
Republic of China, Taiwan, Hong Kong S.A.R. and Macau S.A.R.
(collectively, the “Chinese Territories”), and
Kwangdong Pharmaceutical Co., Ltd. (“Kwangdong”) for
the Republic of Korea (“Korea”).
Palatin’s
new product development activities primarily focus on melanocortin
receptor 1 (“MC1r”) agonists, with potential to treat a
number of inflammatory and autoimmune diseases such as dry eye
disease, also known as keratoconjunctivitis sicca, uveitis,
diabetic retinopathy and inflammatory bowel disease. Palatin has
also designed and is developing potential natriuretic peptide
receptor (“NPR”) candidate drugs that are selective for
one or more different natriuretic peptide receptors, including
natriuretic peptide receptor-A (“NPR-A”), natriuretic
peptide receptor B (“NPR-B”), and natriuretic peptide
receptor C (“NPR-C”), which may be useful in the
treatment of cardiovascular diseases, including reducing cardiac
hypertrophy and fibrosis, heart failure, acute asthma, other
pulmonary diseases and hypertension.
Business Risk and Liquidity –
Since inception, the
Company has incurred negative cash flows from operations, and has
expended, and expects to continue to expend, substantial funds to
complete its planned product development efforts. As shown in the
accompanying consolidated financial statements, the Company had an
accumulated deficit as of September 30, 2018 of $337,227,962 and a
net loss for the three months ended September 30, 2018 of
$5,682,056, and the Company anticipates incurring significant
expenses in the future as a result of spending on its development
programs and will require substantial additional financing or
revenues to continue to fund its planned developmental activities.
To achieve sustained profitability, if ever, the Company, alone or
with others, must successfully develop and commercialize its
technologies and proposed products, conduct successful preclinical
studies and clinical trials, obtain required regulatory approvals
and successfully manufacture and market such technologies and
proposed products. The time required to reach sustained
profitability is highly uncertain, and the Company may never be
able to achieve profitability on a sustained basis, if at
all.
As of
September 30, 2018, the Company’s cash and cash equivalents,
were $32,619,064 and current liabilities were $8,459,905. The
Company intends to utilize existing capital resources for general
corporate purposes and working capital, including, preclinical and
clinical development of our MC1r and MC4r peptide programs and
natriuretic peptide program, and development of other portfolio
products.
Management
believes that the Company’s existing capital resources,
together with proceeds received from sales of common stock in the
Company’s “at-the-market” program (if any), will
be adequate to fund the Company’s planned operations through
at least December 31, 2019. The Company will need additional
funding to complete required clinical trials for its other product
candidates and, assuming those clinical trials are successful, as
to which there can be no assurance, to complete submission of
required applications to the FDA. If the Company is unable to
obtain approval or otherwise advance in the FDA approval process,
the Company’s ability to sustain its operations would be
materially adversely affected.
The
Company may seek the additional capital necessary to fund its
operations through public or private equity offerings,
collaboration agreements, debt financings or licensing
arrangements. Additional capital that is required by the Company
may not be available on reasonable terms, or at all.
10
PALATIN TECHNOLOGIES, INC.
and Subsidiary
Notes to Consolidated Financial Statements
(unaudited)
Concentrations –
Concentrations in the Company’s
assets and operations subject it to certain related risks.
Financial instruments that subject the Company to concentrations of
credit risk primarily consist of cash and cash equivalents and
accounts receivable. The Company’s cash and cash equivalents
are primarily invested in one money market account sponsored by a
large financial institution. For the three months ended September
30, 2018, the Company reported $34,505 in license and contract
revenue related to a license agreement with AMAG for Vyleesi for
North America (“AMAG License Agreement”) (Note 5). For
the three months ended September 30, 2017, the Company reported
$21,941,508 in contract revenue related to the AMAG License
Agreement and $5,000,000 in contract revenue related to Fosun (the
“Fosun License Agreement”) (Note 6)
(2)
BASIS
OF PRESENTATION
The
accompanying unaudited consolidated financial statements have been
prepared in accordance with accounting principles generally
accepted in the United States of America (“U.S. GAAP”)
for interim financial information and with the instructions to Form
10-Q. Accordingly, they do not include all of the information and
footnote disclosures required to be presented for complete
financial statements. In the opinion of management, these
consolidated financial statements contain all adjustments
(consisting of normal recurring adjustments) considered necessary
for fair presentation. The results of operations for the three
months ended September 30, 2018 may not necessarily be indicative
of the results of operations expected for the full
year.
The
accompanying unaudited consolidated financial statements should be
read in conjunction with the audited consolidated financial
statements and notes thereto included in the Company’s Annual
Report on Form 10-K for the year ended June 30, 2018, filed with
the SEC, which includes consolidated financial statements as of
June 30, 2018 and 2017 and for each of the fiscal years in the
three-year period ended June 30, 2018.
(3)
SUMMARY
OF SIGNIFICANT ACCOUNTING POLICIES
Principles of Consolidation
– The consolidated
financial statements include the accounts of Palatin and its
wholly-owned inactive subsidiary. All intercompany accounts and
transactions have been eliminated in consolidation.
Use of Estimates
– The preparation of consolidated
financial statements in conformity with U.S. GAAP requires
management to make estimates and assumptions that affect the
reported amounts of assets and liabilities and disclosure of
contingent assets and liabilities at the date of the consolidated
financial statements and the reported amounts of revenues and
expenses during the reporting period. Actual results could differ
from those estimates.
Cash and Cash Equivalents
– Cash and cash equivalents
include cash on hand, cash in banks and all highly liquid
investments with a purchased maturity of less than three months.
Cash equivalents consist of $32,431,016 and $37,808,099 in a money
market account at September 30, 2018 and June 30, 2018,
respectively.
Fair Value of Financial Instruments
– The
Company’s financial instruments consist primarily of cash
equivalents, accounts receivable, accounts payable and notes
payable. Management believes that the carrying values of cash
equivalents, accounts receivable and accounts payable are
representative of their respective fair values based on the
short-term nature of these instruments. Management believes that
the carrying amount of its notes payable approximates fair value
based on terms of the notes.
Credit Risk
– Financial instruments which potentially
subject the Company to concentrations of credit risk consist
principally of cash and cash equivalents. Total cash and cash
equivalent balances have exceeded insured balances by the Federal
Depository Insurance Company (“FDIC”).
Property and Equipment
– Property and equipment
consists of office and laboratory equipment, office furniture and
leasehold improvements and includes assets acquired under capital
leases. Property and equipment are recorded at cost. Depreciation
is recognized using the straight-line method over the estimated
useful lives of the related assets, generally five years for
laboratory and computer equipment, seven years for office furniture
and equipment and the lesser of the term of the lease or the useful
life for leasehold improvements. Amortization of assets acquired
under capital leases is included in depreciation expense.
Maintenance and repairs are expensed as incurred while expenditures
that extend the useful life of an asset are capitalized.
Accumulated depreciation and amortization was $2,352,603 and
$2,338,558 as of September 30, 2018 and June 30, 2018,
respectively.
11
PALATIN TECHNOLOGIES, INC.
and Subsidiary
Notes to Consolidated Financial Statements
(unaudited)
Impairment of Long-Lived Assets
– The Company reviews
its long-lived assets for impairment whenever events or changes in
circumstances indicate that the carrying amount of the assets may
not be fully recoverable. To determine recoverability of a
long-lived asset, management evaluates whether the estimated future
undiscounted net cash flows from the asset are less than its
carrying amount. If impairment is indicated, the long-lived asset
would be written down to fair value. Fair value is determined by an
evaluation of available price information at which assets could be
bought or sold, including quoted market prices, if available, or
the present value of the estimated future cash flows based on
reasonable and supportable assumptions.
Revenue Recognition
–
In
May 2014, the Financial Accounting Standards Board
(“FASB”) issued Accounting Standards Update
(“ASU”) No. 2014-09,
Revenue from Contracts with
Customers
(“ASC Topic
606”), which, along with amendments from 2015 and 2016
requires an entity to recognize the amount of revenue to which it
expects to be entitled for the transfer of promised goods or
services to customers. ASC Topic 606 replaced most existing revenue
recognition guidance in U.S. GAAP when it became
effective.
On July 1, 2018, the Company adopted ASC Topic 606 using the
modified retrospective approach, a practical expedient permitted
under ASC Topic 606, and applied this approach only to contracts
that were not completed as of July 1, 2018. The Company calculated
a one-time cumulative transition adjustment of $500,000 which was
recorded on July 1, 2018 to the opening balance of accumulated
deficit related to its license agreement with Kwangdong (the
“Kwangdong License Agreement”) as the Company
determined a significant revenue reversal would not occur in a
future period. The one-time adjustment consisted of the recognition
of $500,000 of deferred revenue.
Revenue recognition for periods prior to July 1, 2018
The
Company has generated revenue solely through license and
collaboration agreements. Prior to July 1, 2018, the Company
recognized revenue in accordance with FASB ASC Topic 605-25,
Revenue Recognition for
Arrangements with Multiple Elements
, which addressed the
determination of whether an arrangement involving multiple
deliverables contained more than one unit of accounting. A
delivered item within an arrangement was considered a separate unit
of accounting only if both of the following criteria were
met:
●
the delivered item
had value to the customer on a stand-alone basis; and
●
if the arrangement
included a general right of return relative to the delivered item,
delivery or performance of the undelivered item was considered
probable and substantially in control of the vendor.
Under
FASB ASC Topic 605-25, if both of the criteria above were not met,
then separate accounting for the individual deliverables was not
appropriate.
The
Company determined that it was appropriate to recognize such
revenue using the input-based proportional method during the period
of Palatin’s development obligations as defined in the AMAG
License Agreement. Refer to Note 5 for additional
information.
Under
the Fosun License Agreement (Note 6), the Company received
consideration in the form of an upfront license fee payment and
determined that it was appropriate to recognize such consideration
as revenue in the first quarter of fiscal year 2018, which was the
quarter in which the license was granted, since the license had
stand-alone value and the upfront payment received by the Company
was non-refundable.
Under
the Kwangdong License Agreement (Note 7), the Company received
consideration in the form of an upfront license fee payment and
determined that it was appropriate to record such consideration as
deferred revenue because the upfront payment received by the
Company is subject to certain refund provisions.
Revenue
resulting from the achievement of development milestones was
recorded in accordance with the accounting guidance for the
milestone method of revenue recognition. Amounts received prior to
satisfying the revenue recognition criteria were recorded as
deferred revenue on the Company’s consolidated balance
sheet.
12
PALATIN TECHNOLOGIES, INC.
and Subsidiary
Notes to Consolidated Financial Statements
(unaudited)
Revenue recognition for periods commencing July 1,
2018
For
licenses of intellectual property, the Company assesses, at
contract inception, whether the intellectual property is distinct
from other performance obligations identified in the arrangement.
If the licensing of intellectual property is determined to be
distinct, revenue is recognized for nonrefundable, upfront license
fees when the license is transferred to the customer and the
customer can use and benefit from the license. If the licensing of
intellectual property is determined not to be distinct, then the
license will be bundled with other promises in the arrangement into
one performance obligation. The Company needs to determine if the
bundled performance obligation is satisfied over time or at a point
in time. If the Company concludes that the nonrefundable, upfront
license fees will be recognized over time, the Company will need to
assess the appropriate method of measuring proportional
performance.
Regulatory
milestone payments are excluded from the transaction price due to
the inability to estimate the probability of reversal. Revenue
relating to achievement of these milestones will be recognized in
the period in which the milestone is achieved.
Sales-based
royalty and milestone payments resulting from customer contracts
solely or predominately for the license of intellectual property
will only be recognized upon occurrence of the underlying sale or
achievement of the sales milestone in the future and such
sales-based royalties and milestone payments will be recognized in
the same period earned.
The Company recognizes revenue for reimbursements of research and
development costs under collaboration agreements as the services
are performed. The Company records these reimbursements as revenue
and not as a reduction of research and development expenses as the
Company is the principal in the research and development activities
based upon its control of such activities, which is considered part
of its ordinary activities.
Development milestone payments are generally due 30 business days
after the milestone is achieved. Sales milestone payments are
generally due 45 business days after the calendar year in which the
sales milestone is achieved. Royalty payments are generally due on
a quarterly basis 20 business days after being
invoiced.
The cumulative effect of applying ASC Topic 606 to the
Company’s consolidated balance sheet was as
follows:
|
|
Balance at June
30,
2018
|
Net
Adjustment
|
Balance at July
1,
2018
|
|
Deferred
revenue
|
$
500,000
|
$
(500,000
)
|
$
-
|
|
Accumulated
deficit
|
(332,045,906
)
|
500,000
|
(331,545,906
)
|
13
PALATIN TECHNOLOGIES, INC.
and Subsidiary
Notes to Consolidated Financial Statements
(unaudited)
The impact of adoption of ASC Topic 606 on the Company’s
consolidated balance sheet as of September 30, 2018 is as
follows:
|
PALATIN TECHNOLOGIES, INC
.
|
|||
|
and
Subsidiary
|
|||
|
Consolidated
Balance Sheets
|
|||
|
(unaudited)
|
|||
|
|
|
|
|
|
|
Impact of change in
accounting policies
|
||
|
|
As reported
September 30,
2018
|
Adjustments
|
As reported without
adoption of ASC Topic 606
|
|
ASSETS
|
|
|
|
|
Current
assets:
|
|
|
|
|
Cash and cash
equivalents
|
$
32,619,064
|
$
-
|
$
32,619,064
|
|
Accounts
receivable
|
104,189
|
-
|
104,189
|
|
Prepaid expenses
and other current assets
|
420,639
|
-
|
420,639
|
|
Total current
assets
|
33,143,892
|
-
|
33,143,892
|
|
|
|
|
-
|
|
Property and
equipment, net
|
149,990
|
-
|
149,990
|
|
Other
assets
|
338,916
|
-
|
338,916
|
|
Total
assets
|
$
33,632,798
|
$
-
|
$
33,632,798
|
|
|
|
|
-
|
|
LIABILITIES
AND STOCKHOLDERS’ EQUITY
|
|
|
|
|
Current
liabilities:
|
|
|
|
|
Accounts
payable
|
$
1,165,151
|
$
-
|
$
1,165,151
|
|
Accrued
expenses
|
2,020,333
|
-
|
2,020,333
|
|
Notes payable, net
of discount
|
4,305,242
|
-
|
4,305,242
|
|
Other current
liabilities
|
969,179
|
-
|
969,179
|
|
Total current
liabilities
|
8,459,905
|
-
|
8,459,905
|
|
|
|
|
-
|
|
Notes payable, net
of discount
|
-
|
-
|
-
|
|
Deferred
revenue
|
-
|
500,000
|
500,000
|
|
Other non-current
liabilities
|
-
|
-
|
-
|
|
Total
liabilities
|
8,459,905
|
500,000
|
8,959,905
|
|
|
|
|
|
|
Stockholders’
equity:
|
|
|
|
|
Preferred
stock
|
40
|
-
|
40
|
|
Common
stock
|
2,030,321
|
-
|
2,030,321
|
|
Additional paid-in
capital
|
360,370,494
|
-
|
360,370,494
|
|
Accumulated
deficit
|
(337,227,962
)
|
(500,000
)
|
(337,727,962
)
|
|
Total
stockholders’ equity
|
25,172,893
|
(500,000
)
|
24,672,893
|
|
Total liabilities
and stockholders’ equity
|
$
33,632,798
|
$
-
|
$
33,632,798
|
14
PALATIN TECHNOLOGIES, INC.
and Subsidiary
Notes to Consolidated Financial Statements
(unaudited)
ASC Topic 606 did not have an impact on the Company’s
consolidated statements of operations or cash flows.
Research and Development Costs
– The costs of research
and development activities are charged to expense as incurred,
including the cost of equipment for which there is no alternative
future use.
Accrued Expenses –
Third parties perform a significant
portion of the Company’s development activities. The Company
reviews the activities performed under all contracts each quarter
and accrues expenses and the amount of any reimbursement to be
received from its collaborators based upon the estimated amount of
work completed. Estimating the value or stage of completion of
certain services requires judgment based on available information.
If the Company does not identify services performed for it but not
billed by the service-provider, or if it underestimates or
overestimates the value of services performed as of a given date,
reported expenses will be understated or overstated.
Stock-Based Compensation –
The Company charges to
expense the fair value of stock options and other equity awards
granted. Compensation costs for stock-based awards with time-based
vesting are determined using the quoted market price of the
Company’s common stock on the date of grant or for stock
options, the value determined utilizing the Black-Scholes option
pricing model, and are recognized on a straight-line basis, while
awards containing a market condition are valued using multifactor
Monte Carlo simulations. Compensation costs for awards containing a
performance condition are determined using the quoted price of the
Company’s common stock on the date of grant or for stock
options, the value is determined utilizing the Black Scholes option
pricing model, and are recognized based on the probability of
achievement of the performance condition over the service period.
Forfeitures are recognized as they occur.
Income Taxes
– The Company and its subsidiary file
consolidated federal and separate-company state income tax returns.
Income taxes are accounted for under the asset and liability
method. Deferred tax assets and liabilities are recognized for the
future tax consequences attributable to differences between the
financial statement carrying amounts of assets and liabilities and
their respective tax basis and operating loss and tax credit
carryforwards. Deferred tax assets and liabilities are measured
using enacted tax rates expected to apply to taxable income in the
years in which those temporary differences or operating loss and
tax credit carryforwards are expected to be recovered or settled.
The effect on deferred tax assets and liabilities of a change in
tax rates is recognized in the period that includes the enactment
date. The Company has recorded a valuation allowance against its
deferred tax assets based on the history of losses
incurred.
On
December 22, 2017, the U.S. government enacted wide-ranging tax
legislation, the Tax Cuts and Jobs Act (the “2017 Tax
Act”). The 2017 Tax Act significantly revises U.S. tax law
by, among other provisions, (a) lowering the applicable U.S.
federal statutory corporate income tax rate from 35% to 21%, (b)
eliminating or reducing certain income tax deductions, such as
deductions for interest expense, executive compensation expenses
and certain employee expenses, and (c) repealing the federal
alternative minimum tax (“AMT”) and providing for the
refund of existing AMT credits.
The
Company continues to maintain a full valuation allowance against
its net deferred tax assets. Other provisions enacted include a new
provision designed to tax low-taxed income of foreign subsidiaries
(i.e., “GILTI”) and a one-time transition tax on the
deemed repatriation of post-1986 undistributed foreign subsidiary
earnings and profits (“E&P”) from controlled
foreign corporations (“CFC”). The Company does not have
any foreign subsidiaries, and thus these provisions do not
apply.
15
PALATIN TECHNOLOGIES, INC.
and Subsidiary
Notes to Consolidated Financial Statements
(unaudited)
During
the year ended June 30, 2018, the Company recorded income tax
expense of $82,500, which consisted of $500,000 that was withheld
in accordance with tax withholding requirements in the Chinese
Territories related to the Fosun License Agreement (Note 6) and
$82,500, which was withheld in accordance with tax withholding
requirements in Korea related to the Kwangdong License Agreement
(Note 7). The total income tax expense related to withholding
requirements of $582,500 was offset by an income tax benefit of
$500,000, which resulted from the 2017 Tax Act, under which AMT
credits became refundable, and therefore a $500,000 benefit related
to the release of a valuation allowance against an AMT credit was
recorded during the three months ended December 2017. The
Company’s June 30, 2017 tax return was filed during the three
months ended March 31, 2018 and the Company did not incur an AMT
liability. As a result, as of September 30, 2018 and June 30, 2018,
the Company has a current income tax receivable of $218,000 and a
long-term income tax receivable of $282,000 from estimated AMT that
can be refunded in the future.
Net Income (Loss) per Common Share -
Basic and diluted
earnings per common share (“EPS”) are calculated in
accordance with the provisions of FASB ASC Topic 260,
Earnings per Share
, which includes
guidance pertaining to the warrants issued in connection with the
July 3, 2012, December 23, 2014, and July 2, 2015 private placement
offerings and the August 4, 2016 underwritten offering, that were
exercisable for nominal consideration and, therefore, to the extent
not yet exercised were considered in the computation of basic and
diluted net income (loss) per common share. As of November 21,
2017, all warrants exercisable for nominal value had been converted
into common stock.
The
following table is a reconciliation of net (loss) income and the
shares used in calculating basic and diluted net (loss) income per
common share for the three months ended September 30, 2018 and
2017:
|
|
Three Months Ended
September 30,
|
|
|
|
2018
|
2017
|
|
|
|
|
|
Net (loss)
income
|
$
(5,682,056
)
|
$
10,603,630
|
|
|
|
|
|
Denominator:
|
|
|
|
Weighted average
common shares - Basic
|
205,009,278
|
197,112,400
|
|
|
|
|
|
Effect of dilutive
shares:
|
|
|
|
Common stock
equivalents arising from stock options,
|
|
|
|
warrants and
conversion of preferred stock
|
-
|
1,413,791
|
|
Restriced stock
units
|
-
|
2,834,545
|
|
Weighted average
common shares - Diluted
|
205,009,278
|
201,360,736
|
|
|
|
|
|
Net (loss) income
per common share:
|
|
|
|
Basic
|
$
(0.03
)
|
$
0.05
|
|
Diluted
|
$
(0.03
)
|
$
0.05
|
As of
September 30, 2017, common shares issuable upon the exercise of
outstanding options and warrants, excluding outstanding warrants
exercisable for nominal consideration, and the vesting of
restricted stock units amounted in an aggregate of 11,116,667
shares being excluded from the weighted average number of common
shares used in computing diluted net income per common share
because they were anti-dilutive during the period or the minimum
performance requirements or market conditions had not been met. For
the three months ended September 30, 2018, no additional common
shares were added to the computation of diluted EPS because to do
so would have been anti-dilutive. The potential number of common
shares excluded from diluted EPS during the three months ended
September 30, 2018 was 44,454,308.
Included
in the weighted average common shares used in computing basic and
diluted net income (loss) per common share are 3,347,999 and
1,729,250 vested RSUs that have not been issued as of September 30,
2018 and 2017, respectively, due to a provision in the RSU
agreements to delay delivery.
16
PALATIN TECHNOLOGIES, INC.
and Subsidiary
Notes to Consolidated Financial Statements
(unaudited)
(4)
NEW
AND RECENTLY ADOPTED ACCOUNTING PRONOUNCEMENTS
In May
2017, the FASB issued ASU No. 2017-09,
Compensation-Stock Compensation (Topic 718):
Scope of Modification Accounting
, which clarifies when to
account for a change to the terms or conditions of a share-based
payment award as a modification. Under the new guidance,
modification accounting is required only if the fair value, the
vesting conditions, or the classification of the award (as equity
or liability) changes as a result of the change in terms or
conditions. It is effective prospectively for the annual period
ending June 30, 2019 and interim periods within that annual period.
Early adoption is permitted. The Company adopted this guidance
during the three months ended September 30, 2018. The adoption of
this standard did not have a material impact on the Company’s
consolidated financial statements.
In June
2016, the FASB issued ASU No. 2016-13,
Financial Instruments - Credit Losses:
Measurement of Credit Losses on Financial Instruments
which
requires measurement and recognition of expected credit losses for
financial assets held at the reporting date based on historical
experience, current conditions, and reasonable and supportable
forecasts. This is different from the current guidance as this will
require immediate recognition of estimated credit losses expected
to occur over the remaining life of many financial assets. The new
guidance will be effective for the Company on July 1, 2020. Early
adoption will be available on July 1, 2019. The Company is
currently evaluating the effect that ASU No. 2016-13 will have on
its consolidated financial statements and related
disclosures.
In
February 2016, the FASB issued ASU No. 2016-02,
Leases,
related to the recognition of
lease assets and lease liabilities. The new guidance requires
lessees to recognize almost all leases on their balance sheet as a
right-of-use asset and a lease liability, other than leases that
meet the definition of a short- term lease, and requires expanded
disclosures about leasing arrangements. The recognition,
measurement, and presentation of expenses and cash flows arising
from a lease by a lessee have not significantly changed from the
current guidance. Lessor accounting is similar to the current
guidance, but updated to align with certain changes to the lessee
model and the new revenue recognition standard. The new guidance is
effective for the Company on July 1, 2019, with early adoption
permitted. The Company is currently evaluating the impact that ASU
No. 2016-02 will have on its consolidated financial statements and
related disclosures.
In
January 2016, the FASB issued ASU No. 2016-01,
Financial Instruments: Recognition and
Measurement of Financial Assets and Financial Liabilities
.
The new guidance relates to the recognition and measurement of
financial assets and liabilities. The new guidance makes targeted
improvements to GAAP impacting equity investments (other than those
accounted for under the equity method or consolidated), financial
liabilities accounted for under the fair value election, and
presentation and disclosure requirements for financial instruments,
among other changes. The Company adopted this guidance during the
three months ended September 30, 2018. The adoption of this
standard did not have a material impact on the Company’s
consolidated financial statements.
(5)
AGREEMENT
WITH AMAG
On
January 8, 2017, the Company entered into the AMAG License
Agreement. Under the terms of the AMAG License Agreement, the
Company granted to AMAG (i) an exclusive license in all countries
of North America (the “Territory”), with the right to
grant sub-licenses, to research, develop and commercialize products
containing Vyleesi (each a “Product”, and collectively,
“Products”), (ii) a non-exclusive license in the
Territory, with the right to grant sub-licenses, to manufacture the
Products, and (iii) a non-exclusive license in all countries
outside the Territory, with the right to grant sub-licenses, to
research, develop and manufacture (but not commercialize) the
Products.
Following
the satisfaction of certain conditions to closing, the license
agreement became effective on February 2, 2017. On that date, AMAG
paid the Company $60,000,000 as a one-time initial payment.
Pursuant to the terms of and subject to the conditions in the AMAG
License Agreement, AMAG was required to reimburse the Company up to
an aggregate amount of $25,000,000 for reasonable, documented,
direct out-of-pocket expenses incurred by the Company following
February 2, 2017, in connection with the development and regulatory
activities necessary to file an NDA for Vyleesi for HSDD in the
United States related to Palatin’s development
obligations.
17
PALATIN TECHNOLOGIES, INC.
and Subsidiary
Notes to Consolidated Financial Statements
(unaudited)
The
Company determined there was no stand-alone value for the license,
and that the license and the reimbursable direct out-of-pocket
expenses, pursuant to the terms of the License Agreement,
represented a combined unit of accounting which totaled
$85,000,000. The Company recognized revenue of the combined unit of
accounting over the arrangement using the input-based proportional
method as the Company completed its development obligations. For
the three months ended September 30, 2017, the Company recognized
$21,941,508 as license and contract revenue. During the three
months ended September 30, 2018, license and contract revenue
included additional billings for AMAG related Vyleesi costs of
$34,505.
In
addition, pursuant to the terms of and subject to the conditions in
the AMAG License Agreement, the Company will be eligible to receive
from AMAG (i) up to $60,000,000 upon FDA approval of Vyleesi,
and (ii) up to $300,000,000 in sales milestone payments based on
achievement of certain annual net sales for all Products in the
Territory.
AMAG is
also obligated to pay the Company tiered royalties on annual net
sales of Products, on a product-by-product basis, in the Territory
ranging from the high single-digits to the low double-digits. The
royalties will expire on a product-by-product and
country-by-country basis until the latest to occur of (i) the
earliest date on which there are no valid claims of the
Company’s patent rights covering such Product in such
country, (ii) the expiration of the regulatory exclusivity period
for such Product in such country and (iii) ten years following the
first commercial sale of such Product in such country. Such
royalties are subject to reductions in the event that:
(a) AMAG must license additional third-party intellectual
property in order to develop, manufacture or commercialize a
Product, or (b) generic competition occurs with respect to a
Product in a given country, subject to an aggregate cap on such
deductions of royalties otherwise payable to the Company. After the
expiration of the applicable royalties for any Product in a given
country, the license for such Product in such country will become a
fully paid-up, royalty-free, perpetual and irrevocable
license.
The
Company engaged Greenhill & Co. LLC (“Greenhill”)
as the Company’s sole financial advisor in connection with a
potential transaction with respect to Vyleesi. Under the
engagement agreement with Greenhill, the Company was obligated to
pay Greenhill a fee equal to 2% of all proceeds and consideration
paid to the Company by AMAG in connection with the AMAG License
Agreement, subject to a minimum fee of $2,500,000. The minimum fee
of $2,500,000, less a credit of $50,000 for an advisory fee
previously paid by the Company, was paid to Greenhill and recorded
as an expense upon the closing of the licensing transaction. This
amount will be credited toward amounts that become due to Greenhill
in the future, provided that the aggregate fee payable to Greenhill
will not be less than 2% of all proceeds and consideration paid to
the Company by AMAG in connection with the AMAG License Agreement.
The Company will pay Greenhill an aggregate total of 2% of all
proceeds and consideration paid to the Company by AMAG in
connection with the License Agreement, including future milestone
and royalty payments, after crediting the $2,500,000 that was paid
to Greenhill upon entering into the AMAG License Agreement. The
Company also reimbursed Greenhill $7,263 for certain expenses
incurred in connection with its advisory services.
Pursuant
to the License Agreement, the Company has assigned to AMAG the
Company’s manufacturing and supply agreements with Catalent
Belgium S.A. to perform fill, finish and packaging of
Vyleesi.
(6)
AGREEMENT
WITH FOSUN:
On
September 6, 2017, the Company entered into the Fosun License
Agreement for exclusive rights to commercialize Vyleesi in the
Chinese Territories. Under the terms of the agreement, the Company
received $4,500,000 in October 2017, which consisted of an upfront
payment of $5,000,000 less $500,000 that was withheld in accordance
with tax withholding requirements in the Chinese Territories and
recorded as an expense during the year ended June 30, 2018. The
Company will receive a $7,500,000 milestone payment when regulatory
approval in Chinese Territories is obtained, provided that a
commercial supply agreement for Vyleesi has been entered into.
Palatin has the potential to receive up to $92,500,000 in
additional sales related milestone payments and high single-digit
to low double-digit royalties on net sales in the licensed
territory. All development, regulatory, sales, marketing, and
commercial activities and associated costs in the licensed
territory will be the sole responsibility of Fosun.
18
PALATIN TECHNOLOGIES, INC.
and Subsidiary
Notes to Consolidated Financial Statements
(unaudited)
(7)
AGREEMENT
WITH KWANGDONG:
On
November 21, 2017, the Company entered into the Kwangdong License
Agreement for exclusive rights to commercialize Vyleesi in
Korea.
Under
the terms of the agreement, the Company received $417,500 in
December 2017, consisting of an upfront payment of $500,000, less
$82,500, which was withheld in accordance with tax withholding
requirements in Korea and recorded as an expense during the year
ended June 30, 2018. Based upon certain refund provisions, the
upfront payment was recorded as non-current deferred revenue at
December 31, 2017. O
n July 1, 2018, in
conjunction with the adoption of ASC Topic 606, a one-time
transition of adjustment of $500,000 was recorded to the opening
balance of accumulated deficit as the Company determined a
significant revenue reversal would not occur in a future
period.
The Company will receive a $3,000,000 milestone
payment based on the first commercial sale in Korea. Palatin has
the potential to receive up to $37,500,000 in additional sales
related milestone payments and mid-single-digit to low double-digit
royalties on net sales in the licensed territory. All development,
regulatory, sales, marketing, and commercial activities and
associated costs in the licensed territory will be the sole
responsibility of Kwangdong.
(8)
PREPAID
EXPENSES AND OTHER CURRENT ASSETS
Prepaid
expenses
and other
current assets consist of the following:
|
|
September
30,
2018
|
June
30,
2018
|
|
Clinical study
costs
|
$
62,453
|
$
145,994
|
|
Insurance
premiums
|
30,986
|
42,605
|
|
Other
|
327,200
|
325,089
|
|
|
$
420,639
|
$
513,688
|
(9)
FAIR
VALUE MEASUREMENTS
The
fair value of cash equivalents is classified using a hierarchy
prioritized based on inputs. Level 1 inputs are quoted prices
(unadjusted) in active markets for identical assets or liabilities.
Level 2 inputs are quoted prices for similar assets and liabilities
in active markets or inputs that are observable for the asset or
liability, either directly or indirectly through market
corroboration, for substantially the full term of the financial
instrument. Level 3 inputs are unobservable inputs based on
management’s own assumptions used to measure assets and
liabilities at fair value. A financial asset’s or
liability’s classification within the hierarchy is determined
based on the lowest level input that is significant to the fair
value measurement.
The
following table provides the assets carried at fair
value:
|
|
Carrying
Value
|
Quoted prices in
active markets(Level 1)
|
Other
quoted/observable inputs (Level
2)
|
Significant
unobservable inputs(Level 3)
|
|
September 30,
2018:
|
|
|
|
|
|
Money market
account
|
$
32,431,016
|
$
32,431,016
|
$
-
|
$
-
|
|
June 30,
2018:
|
|
|
|
|
|
Money market
account
|
$
37,808,099
|
$
37,808,099
|
$
-
|
$
-
|
19
PALATIN TECHNOLOGIES, INC.
and Subsidiary
Notes to Consolidated Financial Statements
(unaudited)
(10)
ACCRUED
EXPENSES
Accrued
expenses
consist of the
following:
|
|
September
30,
2018
|
June
30,
2018
|
|
Clinical study
costs
|
$
673,376
|
$
983,410
|
|
Other research
related expenses
|
662,466
|
590,236
|
|
Professional
services
|
66,062
|
297,731
|
|
Severance
|
555,184
|
115,362
|
|
Other
|
63,245
|
116,282
|
|
|
$
2,020,333
|
$
2,103,021
|
(11)
NOTES PAYABLE:
Notes
payable consist of the following:
|
|
September
30,
2018
|
June
30,
2018
|
|
Notes payable under
venture loan
|
$
4,333,334
|
$
6,333,334
|
|
Unamortized related
debt discount
|
(18,496
)
|
(33,535
)
|
|
Unamortized debt
issuance costs
|
(9,596
)
|
(18,138
)
|
|
Notes
payable
|
4,305,242
|
6,281,661
|
|
|
|
|
|
Less: current
portion
|
4,305,242
|
5,948,763
|
|
|
|
|
|
Long-term
portion
|
$
-
|
$
332,898
|
On
December 23, 2014, the Company closed on a $10,000,000 venture loan
which was led by Horizon Technology Finance Corporation
(“Horizon”). The debt facility is a four-year senior
secured term loan that bears interest at a floating coupon rate of
one-month LIBOR (floor of 0.50%) plus 8.50%, and provides for
interest-only payments for the first eighteen months followed by
monthly payments of principal of $333,333 plus accrued interest
through January 1, 2019. The lenders also received five-year
immediately exercisable Series D 2014 warrants to purchase 666,666
shares of common stock exercisable at an exercise price of $0.75
per share. The Company recorded a debt discount of $267,820 equal
to the fair value of these warrants at issuance, which is being
amortized to interest expense over the term of the related debt.
This debt discount is offset against the note payable balance and
included in additional paid-in capital on the Company’s
balance sheet at September 30, 2018 and June 30, 2018. In addition,
a final incremental payment of $500,000 is due on January 1, 2019,
or upon early repayment of the loan. This final incremental payment
is being accreted to interest expense over the term of the related
debt and is included in other current liabilities on the
consolidated balance sheet as of September 30, 2018. The Company
incurred $209,367 of costs in connection with the loan. These costs
were capitalized as deferred financing costs and are offset against
the note payable balance. These debt issuance costs are being
amortized to interest expense over the term of the related
debt.
20
PALATIN TECHNOLOGIES, INC.
and Subsidiary
Notes to Consolidated Financial Statements
(unaudited)
On July
2, 2015, the Company closed on a $10,000,000 venture loan led by
Horizon. The debt facility is a four-year senior secured term loan
that bears interest at a floating coupon rate of one-month LIBOR
(floor of 0.50%) plus 8.50% and provides for interest-only payments
for the first eighteen months followed by monthly payments of
principal of $333,333 plus accrued interest through August 1, 2019.
The lenders also received five-year immediately exercisable Series
G warrants to purchase 549,450 shares of the Company’s common
stock exercisable at an exercise price of $0.91 per share. The
Company has recorded a debt discount of $305,196 equal to the fair
value of these warrants at issuance, which is being amortized to
interest expense over the term of the related debt. This debt
discount is offset against the note payable balance and is included
in additional paid-in capital on the Company’s balance sheet
at September 30, 2018 and June 30, 2018. In addition, a final
incremental payment of $500,000 is due on August 1, 2019, or upon
early repayment of the loan. This final incremental payment is
being accreted to interest expense over the term of the related
debt and is included in other current liabilities on the
consolidated balance sheet as of September 30, 2018. The Company
incurred $146,115 of costs in connection with the loan agreement.
These costs were capitalized as deferred financing costs and are
offset against the note payable balance. These debt issuance costs
are being amortized to interest expense over the term of the
related debt.
The
Company’s obligations under the 2015 amended and restated
loan agreement, which includes both the 2014 venture loan and the
2015 venture loan, are secured by a first priority security
interest in substantially all of its assets other than its
intellectual property. The Company also has agreed to specified
limitations on pledging or otherwise encumbering its intellectual
property assets. The 2015 amended and restated loan agreement
includes customary affirmative and restrictive covenants, but does
not include any covenants to attain or maintain specified financial
metrics. The loan agreement includes customary events of default,
including payment defaults, breaches of covenants, change of
control and a material adverse change default. Upon the occurrence
of an event of default and following any applicable cure periods, a
default interest rate of an additional 5% may be applied to the
outstanding loan balances, and the lenders may declare all
outstanding obligations immediately due and payable and take such
other actions as set forth in the loan agreement. As of September
30, 2018, the Company was in compliance with all of its loan
covenants.
(12)
STOCKHOLDERS’
EQUITY
Financing Transactions –
On April 20, 2018, the Company entered into an
equity distribution agreement (the “Equity Distribution
Agreement”) with Canaccord Genuity LLC
(“Canaccord”), pursuant to which the Company may, from
time to time, sell shares of the Company’s common
stock
at market prices by
methods deemed to be an “at-the-market offering” as
defined in Rule 415 promulgated under the Securities Act of 1933,
as amended. The Company will pay Canaccord 3.0% of the gross
proceeds as a commission. Between July 1, 2018 and September 30,
2018, a total of 2,225,145 shares of common stock were sold through
Canaccord under the Equity Distribution Agreement for net proceeds
of $2,222,447 after payment of commission fees of $68,735. The
Company has no obligation to sell any shares under the Equity
Distribution Agreement and may at any time suspend solicitation and
offers under the Equity Distribution Agreement.
Stock Purchase Warrants
– During the three months
ended September 30, 2017, the Company issued 12,364,219 shares of
common stock pursuant to the cashless exercise provisions of
warrants at an exercise price of $0.01 per share and received
$114,384 and issued 11,438,356 shares of common stock pursuant to
the exercise of warrants at an exercise price of $0.01 per
share.
Stock Options –
For the three months ended September
30, 2018 and 2017, the Company recorded stock-based compensation
related to stock options of $323,703 and $159,874,
respectively.
In July
2018, the terms of certain options were modified to accelerate
vesting and extend the option life. As a result the Company
recorded additional stock-based compensation of $109,004 during the
three months ended September 30, 2018. There were no such
modifications during the three months ended September 30,
2017.
21
PALATIN TECHNOLOGIES, INC.
and Subsidiary
Notes to Consolidated Financial Statements
(unaudited)
A
summary of stock option activity is as follows:
|
|
Number of
Shares
|
Weighted Average
Exercise Price
|
Weighted Average
Remaining Term in Years
|
Aggregate Intrinsic
Value
|
|
|
|
|
|
|
|
Outstanding - July
1, 2018
|
12,775,462
|
0.76
|
7.7
|
|
|
|
|
|
|
|
|
Granted
|
-
|
-
|
|
|
|
Forfeited
|
(133,851
)
|
0.53
|
|
|
|
Expired
|
(129,150
)
|
1.77
|
|
|
|
|
|
|
|
|
|
Outstanding -
September 30, 2018
|
12,512,461
|
0.75
|
7.5
|
3,320,734
|
|
|
|
|
|
|
|
Exercisable at
September 30, 2018
|
6,263,674
|
$
0.77
|
6.0
|
$
1,659,518
|
|
|
|
|
|
|
|
Expected to vest at
September 30, 2018
|
6,248,787
|
$
0.74
|
9.0
|
$
1,661,216
|
Stock
options granted to the Company’s executive officers and
employees generally vest over a 48-month period, while stock
options granted to its non-employee directors vest over a 12-month
period.
Included
in the options outstanding above are 1,075,000 and 125,000
performance-based options granted in December 2017 to executive
officers and employees, respectively, which vest during a
performance period ending on December 31, 2020, if and upon either
i) as to 100% of the target number of shares upon achievement of a
closing price for the Company’s common stock equal to or
greater than $1.50 per share for 20 consecutive trading days, which
is considered a market condition; or ii) as to thirty percent (30%)
of the target number of shares, upon the acceptance for filing by
the FDA of an NDA for Vyleesi for HSDD in premenopausal women
during the performance period, which is considered a performance
condition; iii) as to fifty percent (50%) of the target number of
shares, upon the approval by the FDA of an NDA for Vyleesi for HSDD
in premenopausal women during the performance period, which is also
considered a performance condition; iv) as to twenty percent (20%)
of the target number of shares, upon entry into a licensing
agreement during the performance period for the commercialization
of Vyleesi for FSD in selected countries, which is also considered
a performance condition. The fair value of these options was
$602,760. The Company is amortizing the fair value over the derived
service period of 1.1 years or upon the attainment of the
performance condition. Pursuant to the FDA acceptance of the NDA
filing of Vyleesi, 30% of the target number of options vested in
June 2018.
Restricted Stock Units –
For the three months ended
September 30, 2018 and 2017, the Company recorded stock-based
compensation related to restricted stock units of $800,878 and
$261,997, respectively.
22
PALATIN TECHNOLOGIES, INC.
and Subsidiary
Notes to Consolidated Financial Statements
(unaudited)
A
summary of restricted stock unit activity is as
follows:
|
|
Number of
RSU's
|
|
Outstanding at July
1, 2018
|
9,323,876
|
|
Granted
|
-
|
|
Forfeited
|
(178,851
)
|
|
Vested
|
(319,817
)
|
|
Outstanding at
September 30, 2018
|
8,825,208
|
Included
in outstanding RSUs in the table above are 3,347,999 vested shares
that have not been issued as of September 30, 2018 due to a
provision in the RSU agreements to delay delivery.
Time-based
restricted stock units granted to the Company’s executive
officers, employees and non-employee directors generally vest over
24 months, 48 months and 12 months, respectively.
In
December 2017, the Company granted 1,075,000 performance-based
restricted stock units to its executive officers and 670,000
performance-based restricted stock units to other employees which
vest during a performance period, ending on December 31, 2020, if
and upon either i) as to 100% of the target number of shares upon
achievement of a closing price for the Company’s common stock
equal to or greater than $1.50 per share for 20 consecutive trading
days, which is considered a market condition; or ii) as to thirty
percent (30%) of the target number of shares, upon the acceptance
for filing by the FDA of an NDA for Vyleesi for HSDD in
premenopausal women during the performance period, which is
considered a performance condition; iii) as to fifty percent (50%)
of the target number of shares, upon the approval by the FDA of an
NDA for Vyleesi for HSDD in premenopausal women during the
performance period, which is also considered a performance
condition; iv) as to twenty percent (20%) of the target number of
shares, upon entry into a licensing agreement during the
performance period for the commercialization of Vyleesi for FSD in
at least two of the following geographic areas (a) four or more
countries in Europe, (b) Japan, (c) two or more countries in
Central and/or South America, (d) two or more countries in Asia,
excluding Japan and China, and (e) Australia, which is also
considered a performance condition. The fair value of these awards
was $913,750 and $569,500, respectively. The Company is amortizing
the fair value over the derived service period of 1.1 years or upon
the attainment of the performance condition. Pursuant to the FDA
acceptance of the NDA filing for Vyleesi, 30% of the target number
of shares vested in June 2018.
(13)
SUBSEQUENT
EVENTS
Between October 1, 2018 and November 8, 2018, a total of 31,300
shares of the Company’s common stock were sold through
Canaccord under the Equity Distribution Agreement for net proceeds
of $30,361 after payment of commission fees of $939.
23
The
following discussion and analysis should be read in conjunction
with the consolidated financial statements and notes to the
consolidated financial statements filed as part of this report and
the audited consolidated financial statements and notes thereto
included in our Annual Report on Form 10-K for the year ended June
30, 2018.
Critical Accounting Policies and Estimates
Except
for the adoption of
Accounting
Standards Update No. 2014-09,
Revenue from Contracts with
Customers
(
Topic
606)
(“ASC Topic 606”), our significant
accounting policies, which are described in the notes to our
consolidated financial statements included in this report and in
our Annual Report on Form 10-K for the year ended June 30, 2018,
have not changed during the three months ended September 30, 2018.
We believe that our accounting policies and estimates relating to
revenue recognition, accrued expenses and stock-based compensation
are the most critical.
Overview
We are
a specialized biopharmaceutical company developing first-in-class
medicines based on molecules that modulate the activity of the
melanocortin and natriuretic peptide receptor systems. Our product
candidates are targeted, receptor-specific therapeutics for the
treatment of diseases with significant unmet medical need and
commercial potential. Our most advanced product candidate is
Vyleesi™, the trade name for bremelanotide, a peptide
melanocortin receptor 4 (MC4r) agonist, for the treatment of
premenopausal women with acquired, generalized HSDD, which is a
type of FSD, defined as low desire with associated distress or
interpersonal difficulty. An NDA has been submitted to the FDA by
our exclusive North American licensee, AMAG Pharmaceuticals, Inc.
(“AMAG”) and accepted for filing by the FDA, with an
FDA decision on approval expected in the first quarter of calendar
year 2019.
Vyleesi.
Vyleesi is an on demand subcutaneous injectable
product for the treatment of HSDD in premenopausal women. Vyleesi
is a synthetic peptide analog of the naturally occurring hormone
alpha-MSH (melanocyte-stimulating hormone). In March 2018, our
exclusive North American licensee for Vyleesi, AMAG, submitted an
NDA to the FDA for Vyleesi for the treatment of HSDD in
premenopausal women, which was accepted for filing and review by
the FDA. The Prescription Drug User Fee Act (“PDUFA”)
date for completion of FDA review of the Vyleesi NDA is March 23,
2019. We have also licensed rights to Vyleesi to Fosun for the
Chinese Territories and Kwangdong for Korea.
Our
Phase 3 studies for HSDD in premenopausal women, called the
RECONNECT studies, consisted of two double-blind
placebo-controlled, randomized parallel group studies comparing the
on demand use of 1.75 mg of Vyleesi versus placebo, in each case,
delivered via a subcutaneous auto-injector. Each trial consisted of
more than 600 patients randomized in a 1:1 ratio to either the
treatment arm or placebo with a 24-week evaluation period. In both
clinical trials, Vyleesi met the pre-specified co-primary efficacy
endpoints of improvement in desire and decrease in distress
associated with low sexual desire as measured using validated
patient-reported outcome instruments.
After
completing the studies, patients had the option to continue in an
open-label safety extension study for an additional 52 weeks.
Nearly 80% of patients who completed the randomized portion of the
study elected to remain in the open-label portion of the study. In
the Phase 3 clinical trials, the most frequent adverse events were
nausea, flushing, and headache, which were generally
mild-to-moderate in intensity and were transient.
We
retain worldwide rights for Vyleesi for HSDD and all other
indications outside North America, Korea and the Chinese
Territories. We are actively seeking potential partners for
marketing and commercialization rights for Vyleesi for HSDD outside
the licensed territories. However, we may not be able to enter into
suitable agreements with potential partners on acceptable terms, if
at all.
Melanocortin Receptor Systems.
There are five melanocortin
receptors, MC1r through MC5r. Modulation of these receptors,
through use of receptor-specific agonists, which activate receptor
function, or receptor-specific antagonists, which block receptor
function, can have significant pharmacological effects. Our new
product development activities primarily focus on MC1r agonists,
with potential to treat a number of inflammatory and autoimmune
diseases such as dry eye disease, also known as
keratoconjunctivitis sicca, uveitis, diabetic retinopathy and
inflammatory bowel disease. We believe that MC1r agonists,
including the MC1r agonist peptides we are developing, have broad
anti-inflammatory effects and appear to utilize mechanisms engaged
by the endogenous melanocortin system in regulation of the immune
system and resolution of inflammatory responses. We are also
developing peptides that are active at more than one melanocortin
receptor, and MC4r agonists, with potential utility in a number of
obesity and metabolic-related disorders, including rare disease and
orphan indications.
24
●
PL-8177, a
selective MC1r agonist peptide, is our lead clinical development
candidate for inflammatory bowel diseases, with potential
applicability for a number of other diseases. We filed an
Investigational New Drug (“IND”) application on PL-8177
in late 2017 and have completed subcutaneous dosing of human
subjects in a Phase 1 single and multiple ascending dose clinical
safety study, with data expected in the fourth quarter of calendar
year 2018. We anticipate starting a clinical study with oral dosing
of PL-8177 in human subjects in the fourth quarter of calendar year
2018, with data expected in the first half of calendar year
2019.
●
PL-8331, a dual
MC1r and MC5r peptide agonist, is a preclinical development
candidate for treating ocular inflammation. We have initiated
IND-enabling preclinical activities with PL-8331, and if results
are favorable, anticipate filing an IND and initiating clinical
trials for treatment of dry eye disease in the second half of
calendar year 2019.
●
We have initiated
preclinical programs with MC4r peptides and orally-active small
molecules for treatment of rare genetic metabolic and obesity
disorders, and if results are favorable, anticipate selecting a
lead clinical development candidate and completing IND-enabling
activities in calendar year 2019.
Natriuretic Peptide Receptor Systems.
The natriuretic
peptide receptor (“NPR”) system has numerous
cardiovascular functions, and therapeutic agents modulating this
system may be useful in treatment of cardiovascular diseases,
including reducing cardiac hypertrophy and fibrosis, heart failure,
acute asthma, other pulmonary diseases and hypertension. While the
therapeutic potential of modulating this system is well
appreciated, development of therapeutic agents has been difficult
due, in part, to the short biological half-life of native peptide
agonists. We have designed and are developing potential NPR
candidate drugs that are selective for one or more different
natriuretic peptide receptors, including natriuretic peptide
receptor-A (“NPR-A”), natriuretic peptide receptor B
(“NPR-B”), and natriuretic peptide receptor C
(“NPR-C”).
●
PL-3994 is an NPR-A
agonist we developed which has completed Phase 1 clinical safety
studies. It has potential utility in treatment of a number of
cardiovascular diseases, including genetic and orphan diseases
resulting from a deficiency of endogenous active NPR-A. We have
ongoing academic collaborations with several institutions with
PL-3994.
●
PL-5028, a dual
NPR-A and NPR-C agonist we developed, is in preclinical development
for cardiovascular diseases, including reducing cardiac hypertrophy
and fibrosis. We have ongoing academic collaborations with several
institutions related to PL-5028, and seek to enter into a
development partnership by the end of calendar year
2019.
The
following chart illustrates the status of our drug development
programs.
25
Our Strategy
Key
elements of our business strategy include:
●
Using our
technology and expertise to develop and commercialize products in
our active drug development programs;
●
Entering into
strategic alliances and partnerships with pharmaceutical companies
to facilitate the development, manufacture, marketing, sale and
distribution of product candidates that we are
developing;
●
Partially funding
our product development programs with the cash flow generated from
existing license agreements, as well as any future research,
collaboration or license agreements; and
●
Completing
development and seeking regulatory approval of certain of our other
product candidates.
We were
incorporated under the laws of the State of Delaware on November
21, 1986 and commenced operations in the biopharmaceutical area in
1996. Our corporate offices are located at 4B Cedar Brook Drive,
Cranbury, New Jersey 08512 and our telephone number is (609)
495-2200. We maintain an Internet site at
www.palatin.com
, where among other
things, we make available free of charge on and through this
website our Forms 3, 4 and 5, annual reports on Form 10-K,
quarterly reports on Form 10-Q, current reports on Form 8-K, and
amendments to those reports filed or furnished pursuant to Section
13(a) or 15(d) and Section 16 of the Exchange Act as soon as
reasonably practicable after we electronically file such material
with, or furnish it to, the SEC. Our website and the information
contained in it or connected to it are not incorporated into this
Quarterly Report on Form 10-Q. The reference to our website is an
inactive textual reference only.
Results of Operations
Three Months Ended September 30, 2018 Compared to the Three Months
Ended September 30, 2017:
Revenue –
For the three months ended September 30,
2018, we recognized $34,505 in revenue pursuant to our license
agreement with AMAG compared to $26,941,508 in revenue for the
three months ended September 30, 2017 pursuant to our license
agreements with AMAG and Fosun.
On
January 8, 2017, we entered into the AMAG License Agreement which
provided for $60,000,000 as a one-time initial payment. Pursuant to
the terms of and subject to the conditions in the AMAG License
Agreement, AMAG reimbursed us $25,000,000, less certain expenses
directly paid or to be paid by AMAG, for reasonable, documented,
direct out-of-pocket expenses we incurred following the effective
date of the License Agreement in connection with development and
regulatory activities necessary to file an NDA for Vyleesi for HSDD
in the United States. For the three months ended September 30,
2017, we recognized $21,941,508 of revenue related to this
agreement using the input-based proportional method.
On
September 6, 2017, we entered into the Fosun License Agreement for
exclusive rights to commercialize Vyleesi in the Chinese
Territories, which provided for $5,000,000 as a one-time
non-refundable upfront payment, which was recorded as revenue for
during the three months ended September 30, 2017. Pursuant to the
Fosun License Agreement, $500,000 was withheld in accordance with
tax withholding requirements in the Chinese Territories and was
recorded as an expense during the year ended June 30,
2018.
Research and Development
– Research and development
expenses were $3,622,691 for the three months ended September 30,
2018 compared to $14,163,097 for the three months ended September
30, 2017. The decrease related primarily to completion of our
Vyleesi Phase 3 clinical trial program and ancillary studies
necessary to file an NDA for Vyleesi for HSDD in March
2018.
Research
and development expenses related to our Vyleesi, PL-3994, PL-8177,
MC1r, MC4r and other preclinical programs were $1,944,240 and
$13,185,106 for the three months ended September 30, 2018 and 2017,
respectively. Spending to date has been primarily related to our
Vyleesi for the treatment of HSDD program. The decrease in research
and development expenses is mainly attributable to the conclusion
of Phase 3 clinical trial and development of Vyleesi for HSDD in
March 2018. The amount of such spending and the nature of future
development activities are dependent on a number of factors,
including primarily the availability of funds to support future
development activities, success of our clinical trials and
preclinical and discovery programs, and our ability to progress
compounds in addition to Vyleesi, PL-8177 and PL-3994 into human
clinical trials.
26
The
amounts of project spending above exclude general research and
development spending, which was $1,678,451 and $977,991 for the
three months ended September 30, 2018 and 2017, respectively. The
increase in general research and development spending is primarily
attributable to an increase in stock-based
compensation.
Cumulative
spending from inception to September 30, 2018 was approximately
$307,000,000 on our Vyleesi program and approximately $133,900,000
on all of our other programs (which include PL-3994, PL-8177, other
melanocortin receptor agonists, other discovery programs and
terminated programs). Due to various risk factors described in our
Annual Report on Form 10-K for the year ended June 30, 2018, under
“Risk Factors,” including the difficulty in currently
estimating the costs and timing of future Phase 1 clinical trials
and larger-scale Phase 2 and Phase 3 clinical trials for any
product under development, we cannot predict with reasonable
certainty when, if ever, a program will advance to the next stage
of development or be successfully completed, or when, if ever,
related net cash inflows will be generated.
General and Administrative
– General and
administrative expenses, which consist mainly of compensation and
related costs, were $2,040,582 for the three months ended September
30, 2018 compared to $1,544,575 for the three months ended
September 30, 2017. The increase in general and administrative
expenses is primarily attributable to an increase in
employee-related expenses recognized during the three months ended
September 30, 2018.
Other Income (Expense)
– Total other expense, net was
$(53,288) and $(404,951) for the three months ended September 30,
2018 and 2017, respectively. For the three months ended September
30, 2018, we recognized $(206,871) of interest expense primarily
related to our venture debt offset by $153,583 of investment
income. For the three months ended September 30, 2017, we
recognized $(456,677) of interest expense primarily related to our
venture debt offset by $51,726 of investment income. Interest
expense has decreased as we pay down our venture debt.
Income Taxes
– No income tax expense was recorded for
the three months ended September 30, 2018. Income tax expense was
$225,255 for the three months ended September 30, 2017 related to
the foreign withholding tax requirements of the Fosun License
Agreement.
Liquidity and Capital Resources
Since
inception, we have incurred net operating losses, primarily related
to spending on our research and development programs. We have
financed our net operating losses primarily through debt and equity
financings and amounts received under collaborative and license
agreements.
Our
product candidates are at various stages of development and will
require significant further research, development and testing and
some may never be successfully developed or commercialized. We may
experience uncertainties, delays, difficulties and expenses
commonly experienced by early stage biopharmaceutical companies,
which may include unanticipated problems and additional costs
relating to:
●
the development and
testing of products in animals and humans;
●
product approval or
clearance;
●
regulatory
compliance;
●
good manufacturing
practices (“GMP”) compliance;
●
intellectual
property rights;
●
product
introduction;
●
marketing, sales
and competition; and
●
obtaining
sufficient capital.
Failure
to enter into or successfully perform under collaboration
agreements and obtain timely regulatory approval for our product
candidates and indications would impact our ability to increase
revenues and could make it more difficult to attract investment
capital for funding our operations. Any of these possibilities
could materially and adversely affect our operations and require us
to curtail or cease certain programs.
During
the three months ended September 30, 2018, net cash used in
operating activities was $5,537,562 compared to net cash provided
by operating activities of $1,434,855 for the three months ended
September 30, 2017. The difference in cash used in operations for
the three months ended September 30, 2018 compared with cash
provided by operating activities during the three months ended
September 2017 was the result of lower cash receipts relating to
the AMAG License Agreemnet.
27
During
the three months ended September 30, 2018, net cash used in
investing activities was $0 compared to $9,500 for the three months
ended September 30, 2017. The difference in cash used in investing
activities for the three months ended September 30, 2018 compared
to the three months ended September 2017 was the result of
acquisition of equipment.
During
the three months ended September 30, 2018, net cash provided by
financing activities was $156,455, which consisted of proceeds from
the sale of common stock of $2,222,247 in our
“at-the-market” program, offset by payment on notes
payable obligations of $2,000,000 and withholding taxes related to
restricted stock units of $65,992. During the three months ended
September 30, 2017, net cash used in financing activities was
$1,917,106, which consisted of payments on notes payable
obligations of $2,000,000, withholding taxes related to restricted
stock units of $24,380, and capital lease obligations of $7,110,
offset by proceeds from the exercise of warrants of
$114,384.
We have
incurred cumulative negative cash flows from operations since our
inception, and have expended, and expect to continue to expend in
the future, substantial funds to complete our planned product
development efforts. Continued operations are dependent upon our
ability to complete equity or debt financing activities and enter
into licensing or collaboration arrangements. As of September 30,
2018, our cash and cash equivalents were $32,619,064 and our
current liabilities were $8,459,905.
We
intend to utilize existing capital resources for general corporate
purposes and working capital, including Vyleesi, preclinical and
clinical development of our MC1r and MC4r peptide programs and
natriuretic peptide program, and development of other portfolio
products.
We
believe that our existing capital resources, together with proceeds
received from sales of common stock in our
“at-the-market” program (if any), will be adequate to
fund our planned operations through at least December 31, 2019. We
will need additional funding to complete required clinical trials
for our product candidates and development programs other than
Vyleesi and, if those clinical trials are successful (which we
cannot predict), to complete submission of required regulatory
applications to the FDA.
We
expect to incur significant expenses as we continue our development
of natriuretic peptide and MC1r products. These expenses, among
other things, have had and will continue to have an adverse effect
on our stockholders’ equity, total assets and working
capital. The time required to reach sustained profitability is
highly uncertain, and we do not know whether we will be able to
achieve profitability on a sustained basis, if at all.
Off-Balance Sheet Arrangements
None.
Not
required to be provided by smaller reporting
companies.
Our
management, with the participation of our Chief Executive Officer
and Chief Financial Officer, has evaluated the effectiveness of our
disclosure controls and procedures, as defined in Exchange Act
Rules 13a-15(e) and 15d-15(e), as of the end of the period covered
by this report. Based on that evaluation, our Chief Executive
Officer and Chief Financial Officer concluded that our disclosure
controls and procedures were effective as of September 30, 2018.
There were no changes in our internal control over financial
reporting that occurred during our most recent fiscal quarter that
materially affected, or that are reasonably likely to materially
affect, our internal control over financial
reporting.
28
We may
be involved, from time to time, in various claims and legal
proceedings arising in the ordinary course of our business. We are
not currently a party to any claim or legal
proceeding.
This
report and other documents we file with the SEC contain
forward-looking statements that are based on current expectations,
estimates, forecasts and projections about us, our future
performance, our business, our beliefs and our management’s
assumptions. These statements are not guarantees of future
performance, and they involve certain risks, uncertainties and
assumptions that are difficult to predict. You should carefully
consider the risks and uncertainties facing our
business.
There
have been no material changes to our risk factors disclosed in Part
I, Item 1A, of our Annual Report on Form 10-K for the year ended
June 30, 2018.
Issuer purchases of equity securities.
We have not and do
not currently intend to retire or repurchase any of our capital
securities other than providing our employees with the option to
withhold shares to satisfy tax withholding amounts due from
employees upon the vesting of restricted stock units in connection
with our 2011 Stock Incentive Plan. The following 67,038 shares
were withheld during the quarter ended September 30, 2018 at the
direction of the employees as permitted under the 2011 Stock
Incentive Plan in order to pay the minimum amount of tax liability
owed by the employee from the vesting of those units:
|
Period
|
Total Number of
Shares Purchased (1)
|
Weighted Average
Price Paid per Share
|
Total Number of
Shares Purchased as Part of Publicly Announced Plans or
Programs
|
Maximum Number of
Shares that May Yet be Purchased Under Announced Plans or
Programs
|
|
July 1-31,
2018
|
42,052
|
$
0.95
|
-
|
-
|
|
August 1-31,
2018
|
24,986
|
0.91
|
-
|
-
|
|
September 1-30,
2018
|
-
|
-
|
-
|
-
|
|
Total
|
67,038
|
$
0.94
|
-
|
-
|
(1)
Consists solely of 67,038 shares that were withheld to satisfy tax
withholding amounts due from employees upon the vesting of
previously issued restricted stock units.
None.
Not
applicable.
None.
29
Exhibits
filed or furnished with this report:
|
Exhibit Number
|
Description
|
Filed Herewith
|
Form
|
Filing Date
|
SEC File No.
|
|
Certification
of Chief Executive Officer.
|
X
|
|
|
|
|
|
Certification
of Chief Financial Officer.
|
X
|
|
|
|
|
|
Certification
of principal executive officer pursuant to 18 U.S.C. Section 1350,
as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of
2002.
|
X
|
|
|
|
|
|
Certification
of principal financial officer pursuant to 18 U.S.C. Section 1350,
as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of
2002.
|
X
|
|
|
|
|
|
101.INS
|
XBRL
Instance Document.
|
X
|
|
|
|
|
101.SCH
|
XBRL
Taxonomy Extension Schema Document.
|
X
|
|
|
|
|
101.CAL
|
XBRL
Taxonomy Extension Calculation Linkbase Document.
|
X
|
|
|
|
|
101.LAB
|
XBRL
Taxonomy Extension Label Linkbase Document.
|
X
|
|
|
|
|
101.PRE
|
XBRL
Taxonomy Extension Presentation Linkbase Document.
|
X
|
|
|
|
|
101.DEF
|
XBRL
Taxonomy Extension Definition Linkbase Document.
|
X
|
|
|
|
30
SIGNATURES
Pursuant
to the requirements of the Securities Exchange Act of 1934, the
registrant has duly caused this report to be signed on its behalf
by the undersigned thereunto duly authorized.
|
|
|
Palatin Technologies, Inc.
|
|
|
|
|
(Registrant)
|
|
|
|
|
|
|
|
|
|||
|
|
|||
|
|
|
/s/
Carl Spana
|
|
|
Date:
November 9, 2018
|
|
Carl
Spana, Ph.D.
President
and
Chief
Executive Officer (Principal
Executive
Officer)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
/s/ Stephen T. Wills
|
|
|
Date:
November 9, 2018
|
|
Stephen
T. Wills, CPA, MST
Executive
Vice President, Chief Financial Officer and Chief Operating
Officer
(Principal
Financial and Accounting Officer)
|
|
31
TABLE OF CONTENTS
Part IItem 1. Financial StatementsItem 2. Management S Discussion and Analysis Of Financial Condition and Results Of OperationsItem 3. Quantitative and Qualitative Disclosures About Market RiskItem 4. Controls and ProceduresPart II Other InformationItem 1. Legal ProceedingsItem 1A. Risk FactorsItem 2. Unregistered Sales Of Equity Securities and Use Of ProceedsItem 3. Defaults Upon Senior SecuritiesItem 4. Mine Safety DisclosuresItem 5. Other InformationItem 6. Exhibits