FDA approves drug for loss of sexual desire in women [Reuters (UK)]

Palatin Technologies, Inc. (PTN)
NASDAQ:AMEX Investor Relations:
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Source: Reuters
FDA approves drug for loss of sexual desire in women - Reuters 3 Min Read (Reuters) - The U.S. drug regulator on Friday approved Palatin Technologies and Amag Pharmaceuticals’ drug to restore sexual desire in premenopausal women, the latest attempt to come up with a therapy that some have dubbed as “female Viagra”. The therapy, Vyleesi, will compete in a market which has seen previous attempts fail. Analysts have said that a drug that safely and effectively treats loss of sexual desire in women could eventually reach annual sales of about $1 billion. Palatin’s shares jumped 44% to $1.93, while Amag shares rose 11.5% after market. Vyleesi, chemically known as bremelanotide, activates pathways in the brain involved in sexual desire,
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News
- Palatin Announces MC4R Agonist Bremelanotide Co-Administered with GLP-1/GIP Tirzepatide Meets Primary Endpoint in Phase 2 Obesity Study [Yahoo! Finance]Yahoo! Finance
- Palatin Announces MC4R Agonist Bremelanotide Co-Administered with GLP-1/GIP Tirzepatide Meets Primary Endpoint in Phase 2 Obesity StudyPR Newswire
- Palatin Announces Positive Topline Results from Phase 2 Ulcerative Colitis (UC) Study of Oral Melanocortin-1 Receptor Agonist PL8177PR Newswire
- Palatin's Oral MC4R Agonist PL7737 Receives FDA Orphan Drug Designation for Obesity Due to Leptin Receptor Deficiency [Yahoo! Finance]Yahoo! Finance
- Palatin's Oral MC4R Agonist PL7737 Receives FDA Orphan Drug Designation for Obesity Due to Leptin Receptor DeficiencyPR Newswire
PTN
Earnings
- 2/13/25 - Beat
PTN
Sec Filings
- 4/2/25 - Form RW
- 4/2/25 - Form RW
- 3/31/25 - Form S-1
- PTN's page on the SEC website