Breaking News, Trials & Filings

FDA Clears Pardes IND Application for COVID Antiviral Candidate

PB-0451 is currently being evaluated in a Phase 1 placebo-controlled study in healthy volunteers evaluating safety, tolerability, and pharmacokinetics.

Author Image

By: Kristin Brooks

Managing Editor, Contract Pharma

Pardes Biosciences, Inc., a clinical-stage biopharmaceutical company developing PBI-0451 as a potential novel direct-acting, oral antiviral drug candidate for the treatment and prevention of SARS-CoV-2 infections and associated diseases (i.e., COVID-19), announced that its Investigational New Drug (IND) application for PBI-0451 has been cleared by the U.S. FDA.   PB-0451 is currently being evaluated in a Phase 1 placebo-controlled, blinded, randomized, dose escalation study in healthy voluntee...

Continue reading this story and get 24/7 access to Contract Pharma for FREE


Already a subscriber? Sign in

Keep Up With Our Content. Subscribe To Contract Pharma Newsletters