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Palatin (PTN) investor relations material
Palatin SEO filing summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.SEO filing summary1 Oct, 2025
Company overview and business model
Focuses on developing first-in-class medicines targeting melanocortin receptor systems for obesity, metabolic, inflammatory, and autoimmune diseases.
Pipeline includes MC4R agonists for obesity, MC1R agonists for inflammatory diseases, and other receptor-specific therapeutics.
Recent strategic partnerships include a research and license agreement with Boehringer Ingelheim for retinal disease therapies.
Sold FDA-approved product Vyleesi for HSDD to Cosette, retaining milestone and royalty rights.
Financial performance and metrics
Reported net loss of $17.3 million for the year ended June 30, 2025, with an accumulated deficit of $459.1 million.
Cash and cash equivalents of $2.6 million as of June 30, 2025, with current liabilities of $8.0 million.
Received €2.0 million upfront and potential for up to €278 million in milestone payments from Boehringer Ingelheim, but no significant near-term milestone revenue expected.
Substantial doubt exists about ability to continue as a going concern without additional funding.
Use of proceeds and capital allocation
Net proceeds of approximately $13.9 million (assuming $10.05 per share) intended for working capital and development of MC4R agonists for obesity and related disorders.
May allocate funds to potential acquisitions or investments in complementary businesses.
Management retains broad discretion over use of proceeds.
How will the going concern doubt be addressed?
What is the timeline for PL9643 Phase 3 enrollment?
What is the status of NYSE American relisting?
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Next Palatin earnings date
Q1 202613 Nov, 2025
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Frequently asked questions
Palatin Technologies, Inc., a biopharmaceutical company, develops targeted receptor-specific therapeutics for the treatment of various diseases in the United States. The Company's lead product candidate is bremelanotide, which is under review by the U.S. Food and Drug Administration (FDA) for the potential treatment of hypoactive sexual desire disorder (HSDD) in premenopausal women; and the treatment of benign prostatic hyperplasia (BPH) in men. The Company has its U.S.-based headquarters and research facility located in Cranbury, New Jersey.
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