Jaguar said the FDA supported a protocol amendment for its clinical trial evaluating a crofelemer powder-for-oral-solution formulation in pediatric patients with intestinal failure due to microvillus inclusion disease. Based on that feedback, the company plans to initiate a single-blind extension phase to continue crofelemer treatment after the double-blind period. Dose selection for the extension phase will be determined by an independent Data Monitoring Committee to maintain blinding for study clinicians and company personnel. Jaguar reported that about 30% of participating patients have completed the double-blind treatment phase. No trial results were reported in the announcement.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Jaguar Health Inc. published the original content used to generate this news brief via ACCESS Newswire (Ref. ID: 202603180900ACCESSWRNAPR_____1148176) on March 18, 2026, and is solely responsible for the information contained therein.
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