Aytu BioPharma Inc. Secures Exclusive Agreement to Commercialize EXXUA for MDD Treatment in the U.S

Reuters
06 Jun
Aytu BioPharma Inc. Secures Exclusive Agreement to Commercialize EXXUA for MDD Treatment in the U.S

DENVER, CO / ACCESS Newswire / June 6, 2025 / Aytu BioPharma, Inc. $(AYTU)$ announced that it has signed an exclusive agreement with Fabre-Kramer Pharmaceuticals to commercialize EXXUA™ (gepirone) extended-release tablets in the United States. EXXUA, a novel antidepressant, is the first-in-class selective serotonin 5HT1a receptor agonist approved by the FDA for treating major depressive disorder (MDD) in adults. The transaction is financed by long-term, healthcare-focused institutional investors, including Nantahala Capital Management and Stonepine Capital Management. Aytu is preparing to launch EXXUA in the U.S. by the fourth quarter of 2025, aiming to make it a central element of their commercial strategy.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Aytu Biopharma Inc. published the original content used to generate this news brief via ACCESS Newswire (Ref. ID: 1036228) on June 06, 2025, and is solely responsible for the information contained therein.

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