Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT05904626Phase 2Recruiting
Phase 2, randomised, double-blind trial in intestinal malabsorption comparing ELGN-2112 with Placebo (2 arms). Primary endpoints: Safety of treatment with ELGN-2112 in preterm infants <26 weeks GA at 42 days and Safety of treatment with ELGN-2112 in IUGR infants 26-32 weeks GA at 42 days. Started Oct 2025; status: recruiting.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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