- Pliant Therapeutics Inc PLRX says that with just two FDA-approved Idiopathic Pulmonary Fibrosis drugs, it believes that is a high unmet need.
- Roche Holdings AG's RHHBY Esbriet and Boehringer Ingelheim's Ofev have around $4 billion combined U.S. sales. However, both drugs have modest efficacy (FVC), do not affect survival, have tolerability issues, and have low persistence rates (~30%).
- PLRX believes PLN-74809 can improve upon existing therapies across efficacy and safety/tolerability profile.
- Topline results from the Phase 2a INTEGRIS-IPF trial are expected in mid-2022. The primary endpoints are safety/tolerability, but key efficacy measures are QLF and FVC.
- Related: Pliant Stock Moves Higher On Positive Data From Pulmonary Fibrosis Trial.
- PLRX believes a 2% change in QLF corresponds to a ~10% change in FVC, which is clinically meaningful.
- A separate Phase 2 trial of 320mg PLN-74809 is underway to accumulate safety data to justify 320mg dose inclusion in the potential Phase 2b dose-ranging trial.
- Regarding the potential development path forward in IPF, the management says it would pursue the Phase 2b/Phase 3 'seamless' design but acknowledges the lack of precedent.
- Initial results from PLN-74809 Primary Sclerosing Cholangitis (PSC) program are expected in 4Q FY22/1Q FY23.
- Price Action: PLRX shares are up 10% at $7.56 during the market session on the last check Wednesday.
© 2024 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.
Comments
Loading...
date | ticker | name | Price Target | Upside/Downside | Recommendation | Firm |
---|
Posted In: Analyst ColorBiotechNewsHealth CareAnalyst RatingsMoversTrading IdeasGeneralBriefswhy it's moving
Benzinga simplifies the market for smarter investing
Trade confidently with insights and alerts from analyst ratings, free reports and breaking news that affects the stocks you care about.
Join Now: Free!
Already a member?Sign in