Clinical Trial ResultsInitial Phase 2a efficacy data from patients treated with IMM-1-104 in combination with chemotherapy are very promising, with an overall response rate of 40% and a Disease Control Rate of 80%.
Investor SentimentInvestor skepticism around IMM-1-104's potential seems to be alleviated by the new data, reflected in a pre-market stock increase of 40%.
Safety And TolerabilityThe safety profile reported here, showing no grade 4 adverse events and only 1 grade 3 rash, validates the company's deep cyclical inhibition approach.