Traws Pharma Inc. has announced interim data from an ongoing randomized, open-label Phase 2 clinical study of ratutrelvir, an investigational oral, ritonavir-free Mpro/3CL protease inhibitor, in patients with mild-to-moderate COVID-19. The interim analysis demonstrated a differentiated clinical profile for ratutrelvir compared to PAXLOVID™, with fewer adverse events and no viral rebounds. The data also indicated activity in patients who are ineligible for Paxlovid, addressing a population with limited treatment options. The final data analysis from the study is expected to be reported in January 2026.
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. Traws Pharma Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9603482-en) on December 17, 2025, and is solely responsible for the information contained therein.