Ascentage Pharma Wins FDA and EMA Clearance for Global Phase III Study of Olverembatinib in Ph+ ALL

Reuters12-05
<a href="https://laohu8.com/S/AAPG">Ascentage Pharma</a> Wins FDA and EMA Clearance for Global Phase III Study of Olverembatinib in Ph+ ALL

Ascentage Pharma Group International has received clearance from both the US Food and Drug Administration (FDA) and the European Medicines Agency $(EMA)$ to conduct a global registrational Phase III study (POLARIS-1; NCT06051409) of olverembatinib in combination with chemotherapy for the first-line treatment of newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL). This approval enables the company to enroll patients across multiple countries, accelerating the potential registration of olverembatinib in the US and European markets.

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