Replimune Says Topline Results From Primary Analysis Of The IGNYTE Clinical Trial Of RP1 Plus Nivolumab In Anti-pd1 Failed Melanoma, Primary Endpoint Data Shows 12-month Overall Response Rate Of 33.6%
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Replimune announced topline results from the primary analysis of the IGNYTE clinical trial of RP1 plus Nivolumab in anti-PD1 failed melanoma. The primary endpoint data shows a 12-month overall response rate of 33.6%.

June 06, 2024 | 11:31 am
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Replimune's IGNYTE clinical trial of RP1 plus Nivolumab in anti-PD1 failed melanoma reported a 12-month overall response rate of 33.6%.
The reported 12-month overall response rate of 33.6% is a critical data point for investors. While it provides some positive insight into the efficacy of RP1 plus Nivolumab, the market reaction may be neutral as the data does not indicate a breakthrough result.
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