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STAT+: What to expect from Gossamer Bio’s late-stage lung disease study
STAT News
Published 3 days ago

STAT+: What to expect from Gossamer Bio’s late-stage lung disease study

STAT News · Feb 19, 2026 · Collected from RSS

Summary

Gossamer Bio will be reporting the outcome of a late-stage study in pulmonary arterial hypertension. Here's what to know.

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Adam Feuerstein is a senior writer and biotech columnist, reporting on the crossroads of drug development, business, Wall Street, and biotechnology. He is also a co-host of the weekly biotech podcast The Readout Loud and author of the newsletter Adam’s Biotech Scorecard. You can reach Adam on Signal at stataf.54.This is the online version of Adam’s Biotech Scorecard, a subscriber-only newsletter. STAT+ subscribers can sign up here to get it delivered to their inbox. Gossamer Bio will be reporting the outcome of a Phase 3 clinical trial in pulmonary arterial hypertension, a progressive lung disease, before the end of February. I’m watching this readout with particular interest because it could help answer one of my favorite biotech questions: Is it ever a good idea to run a Phase 3 study based on a “positive” post-hoc subgroup observed in an otherwise negative Phase 2 study? Never, would normally be my skeptical, absolutist answer, except I’m trying to be more open-minded in my older age. Look at Nektar Therapeutics, which has a drug that was given up for dead but might actually prove to be a blockbuster. It can happen. And in Gossamer’s defense, the Phase 2 study results were modest and disappointing, not an outright failure. The company’s explanations for the mid-stage setback — too many stable, low-risk patients enrolled and Covid pandemic disruptions — are also not unreasonable. STAT+ Exclusive Story Already have an account? Log in This article is exclusive to STAT+ subscribers Unlock this article — plus in-depth analysis, newsletters, premium events, and news alerts. Already have an account? Log in View All Plans To read the rest of this story subscribe to STAT+. Subscribe


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