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 compared to a placebo in treating late active or chronic active AMR in kidney transplant recipients, a significant concern in transplant medicine.
The trial is testing felzartamab, an experimental drug administered via intravenous infusion, against a placebo consisting of a 0.9% saline solution. Felzartamab is intended to improve outcomes for patients experiencing late antibody-mediated rejection post-kidney transplant.
This interventional study is designed with a randomized, parallel assignment model and employs quadruple masking, meaning that participants, care providers, investigators, and outcomes assessors are all blinded to the treatment allocations. The primary purpose of the study is treatment-focused.
The study began on December 3, 2024, with its primary completion and estimated study completion dates yet to be announced. The most recent update was submitted on July 31, 2025, indicating ongoing recruitment efforts.
Biogen’s involvement in this trial could influence its stock performance positively if the results demonstrate felzartamab’s efficacy, potentially setting it apart from competitors in the transplant therapy market. Investors should watch for updates, as successful outcomes could enhance Biogen’s market position.
The study is currently recruiting, with further details available on the ClinicalTrials portal.