Immuron Announces Positive Results Support Travelan® progress to Phase 3 Clinical Trials in the US
MELBOURNE, Australia, March 07, 2024 (GLOBE NEWSWIRE) -- Immuron Limited (ASX: IMC; NASDAQ: IMRN), an Australian based and globally integrated biopharmaceutical company is pleased to announce the interim topline results confirming that a single daily dose of Travelan® is effective in prevention of moderate to severe diarrhea following challenge with enterotoxigenic Escherichia coli (ETEC).
- This interim analysis summarizes the data for a total of 60 subjects who have completed the inpatient challenge component of this current clinical study.
- Last patients last visits are anticipated to commence in April this year and final clinical study report will be completed in H2 2024.
- To learn more about Phase 2 study design, read: U.S. Food and Drug Administration Step 3: Clinical Research
IMM-124E (Travelan®) will be the first product developed with Immuron’s platform technology to proceed into Phase 3 clinical trials. - Immuron is in the process of exploring non-dilutive funding opportunities for these Phase 3 clinical trials.