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Europe Review Pathway Cancer

EU Fast-Track Fail For Another BMS CAR-T Cell Therapy

EMA Review Of Ide-Cel Reverts To Standard Timelines; Orva-Cel Development Program Scrapped

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  • Maureen Kenny
    Maureen Kenny

Executive Summary

Bristol Myers Squibb says it is common for cell and gene therapies to revert to the standard timetable as ide-cel follows liso-cel in losing its accelerated assessment status at the European Medicines Agency. Separately, the company has discontinued development of orva-cel, a CAR-T cell therapy that was earlier in the development pipeline.

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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