Detalimogene Demonstrates Improved Complete Response Rate of 62% at 6 Months
“We are highly encouraged with the preliminary data from our LEGEND study, which support our planned BLA filing,” said Ron Cooper, President and CEO. “Based on the emerging clinical profile and detalimogene’s differentiated ease of use, we continue to believe there is a substantial commercial opportunity for detalimogene if approved.”
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“The initial efficacy data from the Part C studies are consistent with the encouraging efficacy signals we previously reported for Parts A and B of THIO-101, including an 88% disease control rate in third-line NSCLC patients. This measure of efficacy is close to triple the reported outcome for standard-of-care chemotherapy
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