Innate Pharma SA's IPHA data from the Phase 2 expansion cohort (cohort 3) evaluating the monalizumab triplet combination shows preliminary activity and an acceptable safety profile with a low discontinuation rate.
- Cohort 3 is exploring the triplet combination of monalizumab, cetuximab, and durvalumab in the first-line treatment of patients with recurrent or metastatic head and neck squamous cell cancer.
- The data will be presented at the ESMO Immuno-Oncology Congress 2021.
- Monalizumab, Innate's lead partnered asset, is an immune checkpoint inhibitor targeting NKG2A receptors expressed on tumor-infiltrating cytotoxic CD8+ T cells and NK cells.
- As of August 1, 40 patients were enrolled. Thirteen patients had a confirmed response with a 32.5% overall response rate, including three complete responses.
- Seven out of 13 responders were still on treatment. The median duration of response was not yet reached.
- The survival rate at 12 months was 58.6%, and the median overall survival was 15 months.
- AstraZeneca Plc AZN obtained full oncology rights to monalizumab in October 2018 through a co-development and commercialization agreement initiated in 2015.
- Also Read: What Is Happening With Innate Pharma Stock On Friday?
- Price Action: IPHA shares are up 0.20% at $4.99 during the premarket session on the last check Thursday.
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