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Representative image: A modern oncology research lab reviewing thoracic scan data, illustrating the clinical push behind Wenda Pharma’s NHWD-870 breakthrough therapy designation for advanced NUT carcinoma in China.

Medical Devices & Diagnostics

Why Wenda Pharma’s Phase II data puts BET inhibition back in focus for NUT carcinoma

by Pallavi Madhiraju
May 9, 2026
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NUT carcinoma has few options and poor survival. Wenda Pharma’s NHWD-870 may test how fast China can move rare oncology forward.

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Representative image of biopharma laboratory research. Gilead Sciences and Merck’s latest Phase 3 updates highlight the promise of once-weekly HIV treatment with islatravir and lenacapavir, while raising fresh questions over Trodelvy’s lung cancer expansion strategy.

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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 U.S. Food and Drug Administration United States Food and Drug Administration US Food and Drug Administration

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