Ironwood Pharmaceuticals Stock Plunges, FDA Wants Another Trial For Gastrointestinal Drug
Ironwood has engaged
Apraglutide is a once-weekly, long-acting synthetic GLP-2 analog with the potential to treat rare gastrointestinal diseases.
In preparation for the new drug application (NDA) submission, pharmacokinetic analysis indicated that the exposure and dose delivered in the STARS Phase 3 trial were lower than planned due to dose preparation and administration.
Based on the strength of the STARS Phase 3 results, Ironwood believed there was a regulatory path forward.
Following a recent dialogue with the
Ironwood plans to work with the
Apraglutide generated strong safety and efficacy data in the STARS Phase 3 trial. Following an analysis of long-term extension trial data, 27 apraglutide-dosed patients dependent on parenteral support achieved enteral autonomy, which is the ultimate goal for these patients. Consistent with
“We are disappointed in this outcome,”
Apraglutide has the potential to provide “tremendous value to patients with SBS-IF who suffer from increased mortality and reduced quality of life,” McCourt added.
Ironwood initiated the rolling new drug application to the
Price Action: IRWD stock is down 30.28% at
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