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Source document· December 11, 2025

Press Release: Sanofi’s Qfitlia and Cablivi approved in China, expanding care for rare diseases

View original at globenewswire.com
Press Release: Sanofi’s Qfitlia and Cablivi approved in China, expanding care for rare diseases Sanofi’s Qfitlia and Cablivi approved in China, expanding care for rare diseases Qfitlia, the first antithrombin-lowering therapy for hemophilia, can offer consistent protection with as few as six injections a yearCablivi, t…
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  • Qfitlia represents a potentially transformative advancement for the hemophilia community in China, shifting care from treating bleeds as they occur to helping prevent them altogether

    80% confidence
  • Qfitlia has the potential to make prophylaxis more accessible for people with hemophilia worldwide by offering effective bleed protection and simplified administration

    80% confidence
  • The approval of Qfitlia marks a true transition into a new era of non-factor prophylactic treatment for hemophilia in China

    80% confidence
  • Cablivi addresses a critical unmet need for patients facing aTTP/iTTP

    80% confidence
  • Qfitlia significantly reduces disease burden by requiring potentially just six subcutaneous injections annually, eliminating the need for frequent intravenous injections associated with traditional factor therapy

    80% confidence
  • These approvals highlight Sanofi's commitment to delivering meaningful innovation and improving outcomes for people living with rare diseases in China and around the world

    80% confidence

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Sanofi · china approvals 20255 approvals
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Q4 2026 Biotech Catalyst Cluster: Late-Stage Data and PDUFA Dates Converge
Early-to-mid November 2026 is a dense run of clinical readouts and Q3 earnings at AHA, AASLD, ACR and ASH. Mid-cap biotechs (Vir, Mineralys, Arrowhead, Oryzon, Novartis, J&J) are reporting data that feeds into regulatory decisions. The next ones are the ivonescimab BLA (Nov 14) and the lorundrostat PDUFA (Dec 22), followed by ECLIPSE 2/3 and Maritime-1 readouts in Q1 2027. The list also includes an unrelated delisting track (EGM Nov 19, application Jan 25, 2027), and the facts have no AI or fintech content.
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Press Release: Sanofi’s Qfitlia and Cablivi approved in China, expanding care for rare diseases: Source | Via News | fr.via.news