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olverembatinib

olverembatinib: 9 clinical trials tracked.

olverembatinib evidence translation

What we can confirm

9 tracked trials

No verified listed developer

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about olverembatinib, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence2 indications · 2 study sponsors
Clinical Trials (9)

Phase II Study of the Combination of Subcutaneous Blinatumomab and Olverembatinib in Patients With Philadelphia Chromosome (ph)-Positive and/or BCR::ABL1 Positive Acute Lymphoblastic Leukemia (ALL)

NCT07178912·Phase 2
Not yet recruiting

Primary endpoint: safety and adverse events

Interventionalopen60 targetStarted 2026-08Completion 2033-091 site · United StatesM.D. Anderson Cancer Center

An Open-Label, Single-Arm, Phase II Exploratory Study of ABL and JAK Kinase Inhibitors With Chemotherapy and Venetoclax in Adult Patients With Ph-like ALL

Recruiting

Primary endpoint: Rate of flow cytometry-minimal residual disease (flow-MRD) negative complete remission at 3 months after treatment initiation

Interventionalopen92 targetStarted 2026-05Completion 2030-031 site · ChinaInstitute of Hematology & Blood Diseases Hospital, China

Low-intensity Chemotherapy Combined With Targeted-Immunotherapy for Newly Diagnosed Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia: A Prospective Clinical Cohort Study

Not yet recruiting

Primary endpoint: Rate of BCR::ABL1 ≤0.01% at 90 days (after three cycles of treatment)

InterventionalRandomizedopen100 targetStarted 2026-04Completion 2030-03Institute of Hematology & Blood Diseases Hospital, China

An Open-Label, Phase 1 Study to Investigate the Effect of Hepatic Impairment on the Pharmacokinetics of Olverembatinib

NCT07282093·Phase 1·CPHI
Recruiting

Primary endpoint: Maximum observed plasma concentration C(max)

Interventionalopen48 targetStarted 2025-11Completion 2026-101 site · ChinaAscentage Pharma Group Inc.

A Phase 3, Multicenter Trial for Pediatric Philadelphia Chromosome-positive B-Acute Lymphoblastic Leukemia -2025 Project

NCT07152041·Phase 3
Recruiting

Primary endpoint: Day 48 end-of-induction measurable residual diseases (MRD48) after induction remission with olverembatinib and blinatumomab, compared to MRD46 of those treated with dasatinib plus chemotherapy induction (CCCG-ALL-2015 /2020) or from historical cohorts .

Interventionalopen150 targetStarted 2025-03Completion 2030-0624 sites · China, Hong KongInstitute of Hematology & Blood Diseases Hospital, China

A Single-Arm Registrational Phase III Study of Olverembatinib in the Treatment of Patients With SDH-Deficient Gastrointestinal Stromal Tumor (POLARIS-3)

NCT06640361·Phase 3·AAPG
Recruiting

Primary endpoint: Progression-free survival(PFS) rate

Interventionalopen40 targetStarted 2024-11Completion 2029-061 site · ChinaAscentage Pharma Group Inc.

This is a Global, Multi-center, Open-label Randomized and Registrational Phase 3 Study of Olverembatinib (HQP1351) in Patients With Chronic Phase Chronic Myeloid Leukemia

NCT06423911·Phase 3·AAPG
Recruiting

Primary endpoint: MMR rate Part A

InterventionalRandomizedopen285 targetStarted 2024-02Completion 2026-021 site · United StatesAscentage Pharma Group Inc.

A Pivotal Registrational Phase 3 Study of Olverembatinib Combined With Chemotherapy Versus Investigator's Choice of TKI Combined With Chemotherapy in Patients With Newly Diagnosed Ph+ ALL

NCT06051409·Phase 3·CPHI
Recruiting

Primary endpoint: Minimal Residual Disease Negative CR Rate

InterventionalRandomizedopen350 targetStarted 2023-08Completion 2029-0650 sites · Australia, China, Czechia, France…Ascentage Pharma Group Inc.

A Phase Ib Study of the Safety, Pharmacokinetic of Lisaftoclax (APG-2575) Single Agent and in Combination With Homoharringtonine or Azacitidine in Patients With Relapsed/Refractory AML

NCT04501120·Phase 1/Phase 2·CPHI
Recruiting

Primary endpoint: Dose Limiting Toxicities (DLT)

Interventionalopen682 targetStarted 2020-09Completion 2029-0912 sites · ChinaAscentage Pharma Group Inc.