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U.S. and EU regulators approved a global Phase III trial for olverembatinib in newly diagnosed Ph+ ALL patients, with promising early results.
The U.S. FDA and European Medicines Agency have approved Ascentage Pharma to launch a global Phase III trial (POLARIS-1) testing olverembatinib plus chemotherapy for newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) patients.
The trial, already active in China and other regions, aims to evaluate the drug’s efficacy and safety as a first-line treatment.
Early data from the 2025 ASH meeting showed high rates of minimal residual disease negativity after three cycles, especially in high-risk subtypes.
Olverembatinib, already approved in China for resistant CML, has received Breakthrough Therapy Designation and is included in national guidelines.
An agreement with Takeda may lead to global rights outside China, Hong Kong, Macau, and Taiwan.
The drug remains investigational in the U.S. and not yet approved.
Los reguladores de los Estados Unidos y la UE aprobaron un ensayo global de fase III para el olverembatinib en pacientes recién diagnosticados con Ph+ ALL, con resultados tempranos prometedores.