Sanofi ((SNYNF)) announced an update on their ongoing clinical study.
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Sanofi is conducting a study titled ‘A Phase 2b/3, Randomized, Double-blind, Placebo-controlled, Multicenter Study, to Investigate the Efficacy and Safety of Lunsekimig in Adult Participants With Inadequately Controlled Chronic Obstructive Pulmonary Disease (COPD) Characterized by an Eosinophilic Phenotype.’ The study aims to evaluate the efficacy, safety, and tolerability of Lunsekimig in adults with COPD who have an eosinophilic phenotype, a subgroup that may respond differently to treatment.
The intervention being tested is Lunsekimig, a drug administered via subcutaneous injection. It is designed to help manage COPD symptoms in patients with an eosinophilic phenotype, potentially offering a new treatment option for this specific group.
The study is interventional, with participants randomly assigned to one of three groups: two different doses of Lunsekimig or a placebo. It uses a parallel model and quadruple masking to ensure unbiased results. The primary goal is to assess the treatment’s effectiveness.
The study began on September 17, 2025, with a primary completion date expected around 48 weeks later, followed by an 8-week follow-up. The latest update was submitted on October 13, 2025, indicating ongoing recruitment and progress.
This study could significantly impact Sanofi’s stock performance by potentially introducing a new treatment for COPD, a condition affecting millions globally. Success could position Sanofi ahead of competitors in the respiratory treatment market, enhancing investor confidence.
The study is currently ongoing, with more details available on the ClinicalTrials portal.