An international, multicenter, randomized, double-blind, phase 3 pivotal registrational clinical study of APG-2575 (Lisaftoclax) combined with azacitidine in elderly patients with newly diagnosed acute myeloid leukemia (GLORA-3)

Trial status: Authorised Event-free survival (EFS): The interval from the date of randomization to the time point when any of the following “events” occur (whichever occurs first): • Progressive disease; • Disease recurrence after CR/CRi/CRh/MLFS; • Death of any cause (including but not limited to death caused by leukemia or therapeutic drugs); • CR/CRi/CRh/MLFS is not achieved after at least 6 treatment cycles., Complete response (CR) rate: The proportion of patients with complete response in the total analysis population., Overall response rate (ORR): The proportion of patients who have achieved CR, CRi, CRh, MLFS and PR in total analysis population., Composite complete response (CRc) rate: The proportion of patients who have achieved CR, CRi and CRh in total analysis population., Time to response (TTR): The interval from the date of randomization to the date of the first CR, CRi, or CRh., Duration of response (DOR): The interval from the date of confirming response (CR/CRi/CRh) to the date of disease recurrence or death of any cause (whichever occurs first). DOR will be calculated for patients with the best response of CR, CRh and CRi separately., Safety and tolerability of subjects: Treatment emergent adverse events (TEAEs) and treatment related adverse events (TRAEs) will be evaluated., Population pharmacokinetic (Pop PK) parameters of APG-2575., Results of EORTC QLQ C30 (V3) and EuroQol 5-Dimension (EQ-5D) questionnaire. Overall survival (OS): Interval between the date of randomization to the date of death of any cause. Survival time will be censored at the latest known survival date of the subject if death cannot be confirmed.

Event-free survival (EFS): The interval from the date of randomization to the time point when any of the following “events” occur (whichever occurs first): • Progressive disease; • Disease recurrence after CR/CRi/CRh/MLFS; • Death of any cause (including but not limited to death caused by leukemia or therapeutic drugs); • CR/CRi/CRh/MLFS is not achieved after at least 6 treatment cycles., Complete response (CR) rate: The proportion of patients with complete response in the total analysis population., Overall response rate (ORR): The proportion of patients who have achieved CR, CRi, CRh, MLFS and PR in total analysis population., Composite complete response (CRc) rate: The proportion of patients who have achieved CR, CRi and CRh in total analysis population., Time to response (TTR): The interval from the date of randomization to the date of the first CR, CRi, or CRh., Duration of response (DOR): The interval from the date of confirming response (CR/CRi/CRh) to the date of disease recurrence or death of any cause (whichever occurs first). DOR will be calculated for patients with the best response of CR, CRh and CRi separately., Safety and tolerability of subjects: Treatment emergent adverse events (TEAEs) and treatment related adverse events (TRAEs) will be evaluated., Population pharmacokinetic (Pop PK) parameters of APG-2575., Results of EORTC QLQ C30 (V3) and EuroQol 5-Dimension (EQ-5D) questionnaire.

Age group: 65+ years, 18-64 years Gender: Female, Male Target enrollment: 58 participants