Immuron (IMRN) said Friday that the US Naval Medical Research Command has completed an interim analysis for the clinical evaluation of a new oral drug to treat Campylobacter and Enterotoxigenic Escherichia coli.
The NMRC funded the study and Immuron produced a hyperimmune bovine colostrum product for testing in a controlled human infection model, the company said.
The interim results showed 10.4% protective efficacy against moderate to severe campylobacteriosis, Immuron said.
The company said the results are unrelated to its Travelan drug and do not affect its plans to hold end of phase 2 meeting with the US Food and Drug Administration with a view to initiating a phase 3 clinical trial of Travelan in H2 2025.
Immuron shares were 2.6% lower in recent trading.
Price: 2.67, Change: -0.07, Percent Change: -2.55
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