Biogen Inc. ((BIIB)), Biogen ((CC:HTER)) announced an update on their ongoing clinical study.
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Biogen Inc. has initiated a Phase 3 clinical trial titled A Double-Blind, Placebo-Controlled, Multicenter, Randomized Phase 3 Trial Evaluating the Efficacy and Safety of Felzartamab in Kidney Transplant Recipients With Late Antibody-Mediated Rejection (AMR). The study aims to assess the effectiveness of felzartamab, a drug intended to treat late active or chronic active antibody-mediated rejection in kidney transplant patients, compared to a placebo.
The intervention involves administering felzartamab via intravenous infusion to the experimental group, while the control group receives a placebo, specifically a 0.9% saline solution. The primary goal is to determine the treatment’s efficacy and safety.
This interventional study follows a randomized, parallel assignment model with quadruple masking, meaning that participants, care providers, investigators, and outcomes assessors are all blinded to the treatment allocations. The study’s primary purpose is treatment-focused.
The study began on December 3, 2024, with its primary completion and estimated completion dates yet to be announced. The latest update was submitted on August 12, 2025, indicating ongoing recruitment.
The outcome of this study could significantly influence Biogen’s stock performance by potentially enhancing its portfolio with a new treatment option. This development might also impact investor sentiment positively, especially if the results demonstrate significant efficacy. Competitors in the biopharmaceutical industry will be closely monitoring these developments.
The study is currently ongoing, and further details can be accessed on the ClinicalTrials portal.
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