Biogen Inc. ((BIIB)) announced an update on their ongoing clinical study.
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Biogen Inc. is currently conducting a study titled A Randomized, Open-Label, 2-Arm, 2-Part, Parallel Group Study to Assess the Pharmacokinetic Comparability of Subcutaneously Administered Litifilimab (BIIB059) Delivered by 3 Devices (Pre-Filled Syringe, Autoinjector, or On-Body Injector) in Healthy Participants. The study aims to understand how the body processes litifilimab when delivered subcutaneously through different devices, focusing on pharmacokinetic comparability.
The interventions being tested include the drug litifilimab, administered via three devices: a pre-filled syringe (PFS), an autoinjector (AI), and an on-body injector (OBI). These devices are designed to facilitate easier administration, particularly for those with limited manual dexterity or needle phobia.
This interventional study is randomized and follows a parallel assignment model without masking, primarily for treatment purposes. Participants are divided into two parts: one group receives litifilimab via AI or PFS, while the other receives it via OBI or PFS.
The study began on December 15, 2024, with the latest update on August 19, 2025. It is currently recruiting, and the primary completion and estimated completion dates are yet to be announced.
The outcome of this study could influence Biogen’s market position by potentially enhancing the delivery method of litifilimab, thus impacting investor sentiment positively. This development could also affect competitors in the pharmaceutical industry focusing on similar treatments.
The study is ongoing, and further details are available on the ClinicalTrials portal.