Autolus Therapeutics Doses First Patient in Phase 1 Trial of Obe-Cel for Progressive Multiple Sclerosis
Autolus Therapeutics plc has announced the dosing of the first patient in its Phase 1 BOBCAT trial evaluating obecabtagene autoleucel (obe-cel) in patients with progressive multiple sclerosis (PMS). The study, conducted at University College London Hospitals NHS Foundation Trust, will enroll up to 18 adult patients to assess the safety, tolerability, and preliminary efficacy of obe-cel in refractory progressive forms of multiple sclerosis. The primary endpoint is safety and tolerability, with additional data to be collected on efficacy measures. Preliminary results from the trial have not yet been presented.
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