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Macao approves China’s first hemophilia B gene therapy, BBM-H901, for adults with moderate to severe disease.
Belief BioMed's BBM-H901, China’s first gene therapy for hemophilia B, has received approval in Macao for adults with moderate to severe disease, following its 2025 approval in mainland China.
The therapy, developed by Belief BioMed and commercialized by Takeda China, uses a modified virus to deliver a gene that enables sustained factor IX production after a single infusion.
Clinical trials showed a near-zero annualized bleeding rate and significantly improved clotting levels, offering a potential long-term alternative to frequent injections.
The approval marks progress in expanding access to advanced gene therapies in the region.
Macao aprueba la primera terapia genética de hemofilia B de China, BBM-H901, para adultos con enfermedad de moderada a grave.