Palatin Reports Second Quarter Fiscal Year 2025 Financial Results and Provides Business Update

Rhea-AI Summary

Palatin Technologies (PTN) announced financial results for Q2 FY2025 and provided key updates on its clinical programs. The company completed database lock for its Phase 2 obesity co-administration study combining MC4R agonist bremelanotide with GLP-1/GIP dual agonist tirzepatide, with topline results expected by end of February 2025.

Financial highlights for Q2 ended December 31, 2024: Net loss was $2.4 million ($0.12 per share), compared to $7.8 million ($0.56 per share) in Q2 2023. Cash position stood at $3.4 million, with additional $4.3 million raised in February 2025. Operating expenses were $2.6 million.

The company is advancing multiple programs including novel 'next generation' MC4R agonists for obesity treatment, with Phase 1 trials targeted for Q4 2025. Additional pipeline updates include expected topline results from Phase 2 PL8177 study in ulcerative colitis later this quarter.

Positive

• Net loss decreased significantly to $2.4M from $7.8M year-over-year
• Raised additional $4.3M through equity offering in February 2025
• Multiple clinical trials advancing with key data readouts expected in 2025
• Potential for up to $171M from Vyleesi rights sale to Cosette Pharmaceuticals

Negative

• Cash position declined to $3.4M from $9.5M in June 2024
• No product revenue recorded in Q2 FY2025 vs $2.0M in Q2 FY2024
• Company needs additional funding for future operations
• Operating expenses increased due to lower gain from Vyleesi sale

Insights

Financial Analyst

Palatin's Q2 FY2025 results reveal a complex financial picture with both opportunities and challenges. The reduced net loss of $2.4 million compared to last year's $7.8 million appears positive, but this improvement largely stems from non-operational factors like warrant liability adjustments rather than fundamental business improvements.

The current cash position of $3.4 million, even with the additional $4.3 million from February's equity offering, raises significant concerns about the company's runway. Based on the quarterly cash burn of $4.8 million, this funding may only sustain operations for approximately 2-3 quarters, suggesting urgent need for additional capital, particularly with multiple clinical programs advancing.

The imminent readout of the Phase 2 obesity study combining bremelanotide with tirzepatide represents a important catalyst. This study targets a significant market opportunity, as current GLP-1 treatments face limitations including cost barriers ($1,000+ monthly) and post-discontinuation weight regain. The MC4R pathway approach could potentially address these limitations, either as monotherapy or in combination with GLP-1s.

The strategic pivot following the Vyleesi divestiture ($171 million potential deal value) demonstrates management's focus on higher-potential therapeutic areas. The advancement of 'next generation' MC4R agonists, including both weekly peptides and oral formulations, could provide multiple shots on goal in the obesity market, estimated to reach $100 billion by 2030.

However, investors should note that the company's ability to fully capitalize on these opportunities depends on securing additional funding. The mention of "multiple potential funding sources" suggests active discussions, but terms and timing remain uncertain. The recent equity raise's dilutive impact and modest size indicate challenging capital market conditions for the company.

• Phase 2 obesity co-administration study with MC4R agonist bremelanotide plus GLP-1/GIP dual agonist tirzepatide
  • Database lock completed
  • Topline data readout expected later this month
• Novel 'next generation' selective MC4R long-acting peptide and an oral small molecule
  • Multiple clinical trials targeted in calendar year 2025
  • For the treatment of general obesity, weight loss management, and rare MC4R pathway diseases, including hypothalamic obesity
• Phase 2 clinical study of PL8177 oral formulation for the treatment of ulcerative colitis
  • Topline data readout expected later this quarter
• Teleconference and Webcast to be held on February 13, 2025, at 11:00 AM ET

CRANBURY, N.J., Feb. 13, 2025 /PRNewswire/ -- Palatin Technologies, Inc. (NYSE American: PTN), a biopharmaceutical company developing first-in-class medicines based on molecules that modulate the activity of the melanocortin receptor system, today announced financial results for its fiscal second quarter ended December 31, 2024 and the completion of database lock for its Phase 2 obesity co-administration study with melanocortin 4 receptor (MC4R) agonist bremelanotide plus glucagon like peptide-1/gastric inhibitory polypeptide (GLP-1/GIP) dual agonist tirzepatide.

"Reaching database lock for our Phase 2 obesity study is a step forward in our mission to bring an alternative treatment to the millions of patients battling obesity," said Carl Spana, Ph.D., President and Chief Executive Officer of Palatin. "Statistical analysis is underway, and we look forward to reporting topline results later this month."

"GLP-1 receptor agonists are popular for treating obesity, but other options are needed for several reasons: they can cause unwanted side effects, be expensive, lead to long-term dependency, and often result in weight gain after stopping them," continued Dr. Spana. "The MC4R pathway helps control eating and how our bodies use energy. We believe that MC4R agonists, especially the long-acting peptides and oral small molecules we are developing, could be an important way to treat obesity, manage weight loss, and help with rare conditions like hypothalamic obesity. These treatments could work alone or in combination with other therapies."

Business Update

Obesity Programs

• Phase 2 BMT-801 'signal detection' clinical study with MC4R agonist bremelanotide plus a GLP-1/GIP dual agonist tirzepatide:
  • Database lock completed.
  • Topline results expected by the end of February 2025.
  • Primary objective: Demonstrate that co-administration of bremelanotide with tirzepatide is safe and has a significant effect on reducing body weight.
• Novel 'next generation' selective MC4R agonists:
  • Once weekly peptide and oral small molecule ready to advance.
  • Potential for monotherapy or combination (with a GLP-1/GIP agonist) therapy.
  • Treating general obesity, weight loss management, rare/orphan genetically caused MC4R pathway diseases, including hypothalamic obesity.
  • Investigational new drug (IND) enabling activities expected to commence 1Q calendar year 2025.
  • Filing of INDs anticipated 2H of calendar year 2025.
  • Commencement of Phase 1 clinical studies targeted for 4Q calendar year 2025.

Non-Obesity Programs: dry eye disease (DED) and other ocular programs, ulcerative colitis (UC), and diabetic nephropathy programs

• Program specific licensing/collaboration and spinout activities ongoing with multiple deals targeted for calendar year 2025.
• DED
  • FDA agreement on sign and symptom endpoints for remaining two Phase 3 pivotal trial protocols, with patient enrollment prepared to commence 1H calendar year 2025.
• UC
  • Topline results from our Phase 2 clinical study of PL8177 oral formulation for the treatment of UC expected later this quarter.
• Diabetic nephropathy
  • Phase 2B study in patients with Type 2 diabetic nephropathy / reported positive and beneficial results for the majority of patients related to worsening kidney function and disease progression.

Fiscal Second Quarter Ended December 31, 2024 Financial Results

Revenue

Pursuant to the completion of the sale of Vyleesi's worldwide rights for female sexual dysfunction to Cosette Pharmaceuticals for up to $171 million in December 2023, Palatin did not record any product sales to pharmacy distributors, for the second quarter ended December 31, 2024. For the second quarter ended December 31, 2023, gross product sales were $4.3 million and net product revenue was $2.0 million.

Operating Expenses

Total operating expenses were $2.6 million, net of a $2.5 million gain on the sale of Vyleesi for the second quarter ended December 31, 2024, compared to $0.9 million, net of a $7.8 million gain on the sale of Vyleesi for the comparable quarter last year. The increase was mainly the result of the decrease in gain on the sale of Vyleesi to Cosette Pharmaceuticals for the second quarter ended December 31, 2024.

Other (Expense) / Income

Total other income / (expense), net, consists mainly of foreign currency transaction gains and (loss) and the change in fair value of warrant liabilities, which Palatin had recorded as a liability on the consolidated financial statements. For the quarter ended December 31, 2023, Palatin recorded a fair value adjustment loss of $8.1 million and offering expenses of $0.7 million.

Cash Flows

Palatin's net cash used in operations for the quarter ended December 31, 2024, was $4.8 million, compared to net cash used in operations of $10.5 million for the same period in 2023. The decrease in net cash used in operations is mainly due to the decrease on the gain on the sale of Vyleesi during the period and secondarily to working capital changes.

Net Loss

Palatin's net loss for the quarter ended December 31, 2024, was $2.4 million, or $(0.12) per basic and diluted common share, compared to a net loss of $7.8 million, or $(0.56) per basic and diluted common share, for the same period in 2023.

The decrease in net loss for the quarter ended December 31, 2024, over the quarter ended December 31, 2023, was driven primarily by the change in fair values of the warrant liability and the elimination of Vyleesi net product revenue and selling expenses, offset by the decrease on gain on the sale of Vyleesi.

Cash Position

As of December 31, 2024, Palatin's cash and cash equivalents were $3.4 million, compared to cash and cash equivalents of $2.4 million at September 30, 2024, and $9.5 million as of June 30, 2024.

The $3.4 million of cash and cash equivalents as of December 31, 2024, does not include $4.3 million of net proceeds from the equity offering, which closed in February 2025.

The Company is actively engaged with multiple potential funding sources for future operating cash requirements.

Conference Call / Webcast

Palatin will host a conference call and audio webcast on February 13, 2025, at 11:00 a.m. Eastern Time to discuss the results of operations in greater detail and provide an update on corporate developments. Individuals interested in listening to the conference call live can dial 1-888-506-0062 (US) or 1-973-528-0011 (International), conference ID 882092. The audio webcast and replay can be accessed by logging on to the "Investor-Webcasts" section of Palatin's website at http://www.palatin.com. A telephone and audio webcast replay will be available one hour after the completion of the call. To access the telephone reply, dial 1-877-481-4010 (US) or 1-919-882-2331 (International), passcode 52016. The webcast and telephone replay will be available through February 27, 2025.

About Melanocortin 4 Receptor Agonists Effect on Obesity

Genetic analysis has identified the melanocortin 4 receptor (MC4R) of the paraventricular nucleus of the hypothalamus as playing a central role in appetite regulation. Genetic mutations that inhibit signaling in the MC4R pathway lead to hyperphagia, decreased energy expenditure and early-onset obesity; such mutations have been identified as the cause of several rare genetic obesity disorders. Agouti-related peptide is an endogenous antagonist of the MC4R that works with neuropeptide Y to stimulate appetite, whereas MC4R agonists such as α- and β-melanocyte-stimulating hormone promote satiety. Agonism of the MC4R therefore represents an attractive target for potential obesity treatments.

About Melanocortin Receptor Agonists

The melanocortin receptor ("MCR") system has effects on inflammation, immune system responses, metabolism, food intake, and sexual function. 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 medically significant pharmacological effects.

Many tissues and immune cells located in the eye (and other places, for example the gut and kidney) express melanocortin receptors, empowering our opportunity to directly activate natural pathways to resolve disease inflammation.

About Palatin

Palatin is a biopharmaceutical company developing first-in-class medicines based on molecules that modulate the activity of the melanocortin receptor systems, with targeted, receptor-specific product candidates for the treatment of diseases with significant unmet medical need and commercial potential. Palatin's strategy is to develop products and then form marketing collaborations with industry leaders to maximize their commercial potential. For additional information regarding Palatin, please visit Palatin's website at www.Palatin.com and follow Palatin on Twitter at @PalatinTech.

Forward-looking Statements

Statements in this press release that are not historical facts, including statements about future expectations of Palatin Technologies, Inc., such as statements about Palatin products in development, clinical trial results, potential actions by regulatory agencies including the FDA, regulatory plans, development programs, proposed indications for product candidates, and market potential for product candidates are "forward-looking statements" within the meaning of Section 27A of the Securities Act of 1933, Section 21E of the Securities Exchange Act of 1934 and as that term is defined in the Private Securities Litigation Reform Act of 1995. Palatin intends that such forward-looking statements be subject to the safe harbors created thereby. Such forward-looking statements involve known and unknown risks, uncertainties and other factors that could cause Palatin's actual results to be materially different from its historical results or from any results expressed or implied by such forward-looking statements. Palatin's actual results may differ materially from those discussed in the forward-looking statements for reasons including, but not limited to, results of clinical trials, regulatory actions by the FDA and other regulatory and the need for regulatory approvals, Palatin's ability to fund development of its technology and establish and successfully complete clinical trials, the length of time and cost required to complete clinical trials and submit applications for regulatory approvals, products developed by competing pharmaceutical, biopharmaceutical and biotechnology companies, commercial acceptance of Palatin's products, and other factors discussed in Palatin's periodic filings with the Securities and Exchange Commission. Palatin is not responsible for updating events that occur after the date of this press release.

Palatin Technologies^® is a registered trademark of Palatin Technologies, Inc.

 

PALATIN TECHNOLOGIES, INC. and Subsidiary Consolidated Statements of Operations (unaudited)
	Three Months Ended December 31,				Six Months Ended December 31,
	2024		2023		2024		2023
REVENUES
Product revenue, net	$                        -		$         2,034,113		$                        -		$         4,140,090
OPERATING EXPENSES
Cost of products sold	-		97,637		-		97,637
Research and development	3,429,479		5,554,200		9,173,233		10,568,830
Selling, general and administrative	1,681,844		3,032,613		3,702,775		6,232,857
Gain on sale of Vyleesi	(2,500,000)		(7,823,482)		(2,500,000)		(7,823,482)
Total operating expenses	2,611,323		860,968		10,376,008		9,075,842
Income (loss) from operations	(2,611,323)		1,173,145		(10,376,008)		(4,935,752)
OTHER INCOME (EXPENSE)
Investment income	29,044		62,026		107,620		133,656
Foreign currency transaction gain (loss)	143,600		(306,697)		12,000		(146,947)
Interest expense	(3,803)		(1,605)		(9,743)		(12,487)
Offering expenses	-		(696,912)		-		(696,912)
Change in fair value of warrant liabilities	-		(8,073,991)		-		(7,391,591)
Total other income (expense), net	168,841		(9,017,179)		109,877		(8,114,281)
NET LOSS	$       (2,442,482)		$       (7,844,034)		$     (10,266,131)		$     (13,050,033)
Basic and diluted net loss per common share	$                (0.12)		$                (0.56)		$                (0.51)		$                (0.99)
Weighted average number of common shares outstanding used in computing basic and diluted net loss per common share	20,634,887		14,097,757		20,239,997		13,134,228

 

PALATIN TECHNOLOGIES, INC. and Subsidiary Consolidated Balance Sheets (unaudited)
	December 31, 2024		June 30, 2024
ASSETS
Current assets:
Cash and cash equivalents	$                     3,416,604		$           9,527,396
Prepaid expenses and other current assets	253,113		242,272
Total current assets	3,669,717		9,769,668
Property and equipment, net	235,741		388,361
Right-of-use assets - operating leases	347,644		527,321
Other assets	56,916		56,916
Total assets	$                     4,310,018		$         10,742,266
LIABILITIES AND STOCKHOLDERS' DEFICIENCY
Current liabilities:
Accounts payable	$                     6,718,233		$           4,101,929
Accrued expenses	1,650,700		4,185,046
Short-term operating lease liabilities	257,673		380,542
Short-term finance lease liabilities	-		46,014
Other current liabilities	932,150		944,150
Total current liabilities	9,558,756		9,657,681
Long-term operating lease liabilities	100,071		163,782
Other long-term liabilities	1,032,300		1,032,300
Total liabilities	10,691,127		10,853,763
Stockholders' deficiency:
Preferred stock of $0.01 par value – authorized 10,000,000 shares: shares issued
and outstanding designated as follows:
Series A Convertible: authorized 4,030 shares as of December 31, 2024: issued
and outstanding 4,030 shares as of December 31, 2024 and June 30, 2024	40		40
Common stock of $0.01 par value – authorized 300,000,000 shares:
issued and outstanding 23,455,846 shares as of December 31, 2024 and 17,926,640 shares as of June 30, 2024	234,558		179,266
Additional paid-in capital	445,416,974		441,475,747
Accumulated deficit	(452,032,681)		(441,766,550)
Total stockholders' deficiency	(6,381,109)		(111,497)
Total liabilities and stockholders' deficiency	$                     4,310,018		$         10,742,266

 

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SOURCE Palatin Technologies, Inc.

FAQ

When will PTN release topline results for its Phase 2 obesity study?

Palatin expects to release topline results from its Phase 2 obesity co-administration study by the end of February 2025.

What was Palatin's (PTN) net loss for Q2 FY2025?

Palatin reported a net loss of $2.4 million, or $0.12 per basic and diluted common share, for Q2 FY2025 ended December 31, 2024.

How much cash does PTN have as of December 31, 2024?

Palatin had $3.4 million in cash and cash equivalents as of December 31, 2024, plus an additional $4.3 million raised in February 2025.

What are the next major clinical milestones for PTN in 2025?

PTN plans to commence Phase 1 trials for next-generation MC4R agonists in Q4 2025 and expects topline results from its Phase 2 PL8177 ulcerative colitis study in Q1 2025.

How much did PTN receive from the Vyleesi sale to Cosette Pharmaceuticals?

Palatin sold Vyleesi's worldwide rights to Cosette Pharmaceuticals in December 2023 for up to $171 million.