enGene Reports 62% Complete Response Rate for Detalimogene in Bladder Cancer Trial
enGene Holdings Inc. has announced positive preliminary results from the pivotal cohort of its LEGEND trial studying detalimogene voraplasmid (detalimogene, formerly EG-70) in patients with high-risk, BCG-unresponsive non-muscle invasive bladder cancer (NMIBC) with carcinoma in situ (CIS) with or without concomitant papillary disease. The results showed an improved complete response rate of 62% at six months. Safety data from 125 patients demonstrated a favorable tolerability profile, with low rates of treatment-related adverse events (42%) and dose interruptions (1.6%). The company has not specified if these results have already been presented at a scientific meeting or will be presented in the future.
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