Innate Pharma S.A. ((IPHYF)) announced an update on their ongoing clinical study.
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Innate Pharma S.A. is conducting a clinical study titled ‘A Phase II Multicenter, Open Label, Non-randomized Study of Neoadjuvant and Adjuvant Treatment With IPH5201 and Durvalumab in Patients With Resectable, Early-stage (II to IIIA) Non-Small Cell Lung Cancer (MATISSE).’ The study aims to evaluate the safety and efficacy of combining IPH5201 and durvalumab with standard chemotherapy in patients with early-stage non-small cell lung cancer (NSCLC) that is resectable. This research is significant as it explores potential advancements in NSCLC treatment, which could improve patient outcomes.
The intervention being tested involves the use of the drugs IPH5201 and durvalumab, both administered alongside standard chemotherapy. The purpose of this combination is to enhance the treatment’s effectiveness in reducing cancer before surgery (neoadjuvant) and preventing recurrence after surgery (adjuvant).
The study follows an interventional design with a single-group model. There is no allocation or masking involved, meaning all participants receive the same treatment, and both the researchers and participants know what treatment is being administered. The primary goal is treatment-focused, aiming to assess the therapeutic impact of the drug combination.
The study began on February 15, 2023, and is currently recruiting participants. The primary completion date is yet to be determined, with the last update submitted on May 13, 2025. These dates are crucial as they indicate the study’s progress and timeline for potential results.
The update on this study could influence Innate Pharma’s stock performance and investor sentiment, as successful outcomes may lead to advancements in NSCLC treatment options. This could position Innate Pharma favorably against competitors in the oncology sector, potentially driving investor interest and confidence.
The study is ongoing, with further details available on the ClinicalTrials portal.
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