Dec 16 (Reuters) - Medivir AB MVIRb.ST :
* FUTILITY ANALYSIS PERFORMED OF THE PHASE II COMBINATION STUDY WITH BIRINAPANT AND
KEYTRUDA® IN
COLORECTAL CANCER PATIENTS
* PRIMARY OBJECTIVE OF PHASE II STUDY WAS AN IMPROVED CLINICAL RESPONSE TO TREATMENT
MEASURED AS
20% ORR (OVERALL RESPONSE RATE)
* INDEPENDENT SAFETY COMMITTEE RECOMMENDATION IS THAT STUDY SHOULD BE TERMINATED
* INDEPENDENT SAFETY COMMITTEE ANALYSIS INDICATES THAT IT IS UNLIKELY THAT STUDY'S
OBJECTIVES WILL
BE MET
* CO DECIDED TO DISCONTINUE RECRUITMENT OF PATIENTS AND TO END STUDY
Source text for Eikon: ID:nWkr30NyrR
Further company coverage: MVIRb.ST
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