Registro de fonte primária
A empresa anunciou que uma BLA para ivonescimab foi protocolada junto à FDA. Uma data-alvo de ação PDUFA de 14 de novembro de 2026 foi atribuída. Isso estabelece o primeiro cronograma formal de revisão da FDA para o ativo fora da China.
EX-99.2 3 a20260223q4fy2025earning.htm EX-99.2 a20260223q4fy2025earning Summit Therapeutics Q4 & FY 2025 Earnings Call February 23, 2026 4:30pm ET Forward Looking Statement Any statements in this presentation about the Company’s future expectations, plans and prospects, including but not limited to, statements about the clinical and preclinical development of the Company’s product candidates, entry into and actions related to the Company’s partnership with Akeso Inc., the Company's anticipated spending and cash runway, the therapeutic potential of the Company’s product candidates, the potential commercialization of the Company’s product candidates, the timing of initiation, completion and availability of data from clinical trials, the potential submission of applications for marketing a
Summit apresenta dados atualizados de OS do HARMONi no WCLC 2026
Summit inicia ensaio HARMONi-GU1 de Fase II/III de ivonescimab no cancro da bexiga em 1L
Summit: dados de OS do ivonescimab HARMONi-6 no ASCO 2026 Plenary
Summit: Dados do ivonescimab no ELCC 2026 (PFS intracraniana do HARMONi)
Summit, GSK iniciarão ensaio clínico de ivonescimab + ADC B7-H3 em meados de 2026