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Acticor Biotech Announces the Conclusions of the Interim Futility Analysis in the GREEN Study
ACTICOR BIOTECH (FR0014005OJ5 - ALACT), a clinical stage biopharmaceutical company developing glenzocimab, an innovative drug for the treatment of cardiovascular emergencies, announces the conclusions of the futility analysis of the phase 2/3 GREEN study evaluating glenzocimab as an adjunct to
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Acticor Biotech Announces the Conclusions of the Interim Futility Analysis in the GREEN Study By Investing.com
ACTICOR BIOTECH (FR0014005OJ5 - ALACT), a clinical stage biopharmaceutical company developing glenzocimab, an innovative drug for the treatment of cardiovascular emergencies, announces the conclusions of the futility analysis of the phase 2/3 GREEN study evaluating glenzocimab as an adjunct to
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Acticor Biotech's phase 2/3 study of glenzocimab for acute ischemic stroke treatment passes interim futility analysis. The independent Data Monitoring Committee recommends continuing the trial without modification.

Acticor Biotech, a clinical-stage biotechnology company, has announced positive results from the interim futility analysis of its ongoing GREEN study. The study is evaluating glenzocimab, a novel treatment for acute ischemic stroke, in combination with standard of care thrombolysis and/or thrombectomy
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.The independent Data Monitoring Committee (DMC) has recommended the continuation of the GREEN study without any modifications to the protocol. This decision was based on their review of the interim futility analysis, which examined data from the first 100 patients enrolled in the trial
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.The positive outcome of the futility analysis is a crucial milestone for Acticor Biotech. It indicates that glenzocimab shows promise as a potential treatment for acute ischemic stroke, warranting further investigation in the ongoing phase 2/3 study
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.The GREEN study is a randomized, double-blind, multicenter, placebo-controlled, parallel-group phase 2/3 study. It aims to evaluate the efficacy and safety of glenzocimab in combination with standard of care (thrombolysis, thrombectomy, or both) for acute ischemic stroke
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.Glenzocimab is a humanized monoclonal antibody fragment that inhibits platelet glycoprotein VI (GPVI). It is designed to be used in emergency situations as a first-line treatment for acute ischemic stroke, in combination with reperfusion treatments such as thrombolysis and/or thrombectomy
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With the positive outcome of the interim analysis, Acticor Biotech will continue the GREEN study as planned. The company aims to complete patient enrollment by the end of 2023 and expects to have the full results of the study available in Q2 2024
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.Gilles Avenard, CEO of Acticor Biotech, expressed satisfaction with the interim analysis results. He emphasized the importance of this milestone in the development of glenzocimab and reiterated the company's commitment to bringing innovative treatments to stroke patients
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