FDA autoriza ensayo clínico de Treprostinil-Iloprost SMI de United Therapeutics
- La FDA autorizó a United Therapeutics a iniciar un ensayo de fase 1 de Treprostinil-Iloprost SMI, tratamiento inhalado experimental para hipertensión arterial pulmonar.
- El ensayo evaluará seguridad, tolerabilidad y farmacocinética en voluntarios sanos; la fase 2 en pacientes se prevé para 2027, condicionada a resultados favorables.
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. United Therapeutics Corporation published the original content used to generate this news brief via Business Wire (Ref. ID: 202610280700BIZWIRE_USPR_____20261028_BW830210) on October 28, 2026, and is solely responsible for the information contained therein.