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A clinician reviews an investigational treatment as MaaT Pharma prepares to challenge the negative European regulatory opinion on MaaT013 for acute graft-versus-host disease. Representative image.

Pharma & Biotech

MaaT Pharma seeks second review of MaaT013 as regulators question single-arm evidence

by Pallavi Madhiraju
June 26, 2026
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Discover why MaaT Pharma is challenging the negative CHMP opinion on MaaT013 and what the September review means for acute graft-versus-host disease.

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clinical trials Eli Lilly and Company European Medicines Agency FDA FDA approval immuno-oncology immunotherapy Inc. Johnson & Johnson medical devices oncology precision oncology rare disease U.S. Food and Drug Administration United States Food and Drug Administration

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