A Phase II trial evaluating Ironwood Pharmaceuticals’ (NASDAQ:IRWD)
MD-7246 in adult patients with abdominal pain associated with irritable
bowel syndrome with diarrhea (IBS-D) failed to achieve its primary or
key secondary endpoints.
Patients taking MD-7246 experienced no clinically meaningful effect on bowel function.
However, MD-7246 was generally well-tolerated and most adverse events were mild to moderate in severity.
Based on these findings, Ironwood and collaboration partner AbbVie (NYSE:ABBV) plan to discontinue the development of MD-7246.
Ironwood and AbbVie are now further examining the
MD-7246 Phase II data in IBS-D to understand the discordance with the
improvement in pain observed in the previous IBS-C results.
https://seekingalpha.com/news/3577846-ironwood-pharmas-mdminus-7246-flunks-mid-stage-study-in-ibs-d
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