Encouraging signs for GI company's Yeliva study

6 September 2018

RedHill Biopharma (Nasdaq: RDHL), an Israeli biopharma that specializes in gastrointestinal diseases, has met the pre-specified efficacy goal for the first stage of a Phase IIa study of orally-administered Yeliva (opaganib).

This means that RedHill will continue the study in advanced cholangiocarcinoma, or bile duct cancer, into the second stage, enrolling the full cohort of 39 evaluable patients.

The primary efficacy endpoint of the study is defined as either partial or complete response, or stable disease at four months treatment with Yeliva. Enrolment of all subjects is expected to be completed by mid-2019.

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