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Why Palatin Technologies Might Be Worth a Look After Recent Financing

Management and board members participated in the recent financing

Palatin Technologies (NYSE American: $PTN ( ▼ 40.35% ) )* has experienced significant share price pressure, currently trading at around 10 cents despite a series of positive clinical developments across multiple therapeutic areas. The recent $11.5 million financing announcement on May 7, 2025, while dilutive, may come at an inflection point for the company. Let's examine the case for potentially considering the company at these depressed levels.

Addressing Immediate Concerns

Delisting Risk Likely Resolved

The most immediate threat to Palatin has been the NYSE American's determination to delist the company for failing to meet stockholders' equity requirements. However, management believes the recent $11.5 million financing, combined with $2.3 million raised in April through their ATM facility, will be sufficient to resolve this issue. As stated in their May 7, 2025 announcement: "The Company believes the upfront amount of $11.5 million in gross proceeds, combined with approximately $2.3 million in net proceeds received in April 2025 under its at-the-market (ATM) facility, and its current plans and operations will be sufficient to resolve the delisting determination of NYSE American."

Management's Vote of Confidence

In a notably positive signal, the company's announcement specifically mentioned that the CEO, CFO, and certain board members, including the Chair, participated in the latest financing round. As stated in their May 7, 2025 pricing announcement: "Palatin Technologies, Inc. (NYSE American: PTN) ("Palatin" or the "Company")... today announced the pricing of its public offering with participation from new and existing healthcare focused institutional investors along with the Company's Chief Executive Officer, Chief Financial Officer, and certain board members, including the Chair..."

Clinical Assets with Significant Market Potential

Looking beyond immediate financial concerns, Palatin has built an impressive portfolio across four major therapeutic areas:

1. Obesity Program

Palatin's Phase 2 BMT-801 study, combining melanocortin-4 receptor (MC4R) agonist bremelanotide with tirzepatide (GLP-1/GIP), recently met its primary endpoint with highly statistically significant results. According to their March 31, 2025 announcement: "The co-administered group had a 4.4% reduction in weight compared to 1.6% for the placebo group (p<0.0001)." The announcement also noted: "40% of patients in the co-administered group achieved a 5% reduction in their body weight, compared to 27% for the tirzepatide alone group (p<0.05)."

The data also showed that "weight regain was effectively halted in the MC4R agonist bremelanotide group" after treatment cessation. With novel next-generation MC4R long-acting peptides and oral small molecules advancing toward IND applications in Q4 2025, Palatin is positioning itself in the obesity market projected to reach nearly $900 billion by 2035 according to Future Market Insights data included in the provided documents.

2. Ulcerative Colitis Program

PL8177, Palatin's oral melanocortin-1 receptor agonist for ulcerative colitis (UC), recently delivered impressive Phase 2 results. According to their March 28, 2025 announcement: "Clinical response (statistically significant) was demonstrated in 78% (7 of 9) of PL8177-treated patients versus 33% (1 of 3) on placebo (p<0.005)." The same announcement noted: "Clinical remission was achieved in 33% (3 of 9) of PL8177-treated patients versus 0% (0 of 3) on placebo." The global ulcerative colitis market is projected to reach $15.81 billion by 2034, according to market data included in the provided documents.

The company also stated: "Several major pharmaceutical companies have shown strong interest in our UC program, and we believe these positive Phase 2 results in PL8177 treated patients, for the critical efficacy endpoints of both clinical remission and clinical response, could help solidify a potential licensing deal."

3. Dry Eye Disease Program

Palatin's PL9643 for dry eye disease has completed one Phase 3 trial (MELODY-1) with positive results. According to their corporate presentation: "Co-Primary symptom endpoint of pain met statistical significance (P<0.025)" and "7 of 11 Secondary symptom endpoints met statistical significance (P<0.05)." The company is preparing to initiate two additional Phase 3 trials with protocols confirmed by the FDA. In their May 7, 2025 announcement, Dr. Spana stated: "Discussions around collaborations and asset sales for our Phase 3 dry eye disease program, as well as our preclinical glaucoma and retina programs, are progressing well."

4. Diabetic Nephropathy Program

The Phase 2b BREAKOUT study evaluating bremelanotide in patients with Type 2 diabetic nephropathy demonstrated positive results. According to their April 10, 2025 announcement: "71% of patients achieved a >30% reduction in the urine protein to creatinine ratio (UP/Cr), a key indicator of kidney damage" and "71% of patients demonstrated improved or stabilized estimated glomerular filtration rate (eGFR), signaling preserved kidney function." These results were presented at the National Kidney Foundation Spring Meeting in April 2025.

Near-Term Catalysts

Several potential catalysts over the coming months could drive renewed interest in Palatin:

  1. Resolution of delisting concerns through the appeal process (confirmed in their April 14, 2025 announcement)

  2. Partnership announcements for ocular programs expected in Q2-Q3 2025 (stated in May 7, 2025 announcement)

  3. Potential licensing deals for the ulcerative colitis program (mentioned in their March 28, 2025 announcement)

  4. IND submissions for next-generation obesity treatments in Q4 2025 (confirmed in multiple announcements)

  5. Clinical data from Phase 1 SAD/MAD studies expected in H1 2026 (stated in May 7, 2025 announcement)

While the opportunity may be compelling, investors should consider several risks including dilution concerns, clinical development risks, cash runway, and the competitive landscape when conducting their due diligence.

Conclusion

Palatin Technologies presents an interesting case study of a clinical-stage biotech whose market value appears disconnected from its pipeline progress. The company has demonstrated positive clinical results across multiple billion-dollar markets, while management has shown conviction through personal investment in the recent financing.

The expected resolution of delisting concerns, combined with multiple potential partnership catalysts in the coming quarters, may provide an opportunity for contrarian investors willing to accept the risks inherent in clinical-stage biotechnology companies. With multiple shots on goal across diverse therapeutic areas, all based on the company's expertise in melanocortin receptor modulation, Palatin offers an intriguing risk-reward profile at current levels that may be worth considering..