FDA Clears Palatin's IND Application For Phase 2 Study Of Bremelanotide Co-Administered With Tirzepatide For Obesity, The Phase 2 Study Is Expected To Start By Mid-2024, With Topline Data Results By The End Of 2024
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The FDA has approved Palatin Technologies' IND application for a Phase 2 study of Bremelanotide in combination with Tirzepatide for obesity treatment. The study is set to begin by mid-2024, with results expected by the end of 2024.

May 02, 2024 | 11:38 am
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Palatin Technologies receives FDA clearance for Phase 2 obesity study, indicating progress in its product pipeline.
FDA approval for clinical studies is a critical regulatory milestone for biotech companies, often leading to positive investor sentiment. The clearance of Palatin Technologies' IND application for a Phase 2 study signifies a significant step forward in its product development pipeline, potentially addressing a large market in obesity treatment. This development is likely to be viewed positively by investors, potentially leading to an uptick in PTN's stock price in the short term.
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