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Study of HQP1351 in Subjects With Refractory CML and Ph+ ALL

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NCT04260022 · readout in 1,226 d

Sponsored by Ascentage Pharma Group Inc. (industry) · AAPG — their whole pipeline →.

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
242estimated
Sites
9
Countries
Canada, United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2020-01-09actualWhen the study began enrolling
Primary completion2029-12-27estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2030-03-31estimatedThe whole study's end, after follow-up
First posted2020-02-07actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-11-05actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Leukemia, Myeloid, Chronic
  • Myeloid Leukemia
  • Chronic Myeloid Leukemia
  • Philadelphia Positive Acute Lymphoblastic Leukemia
  • B Cell Precursor Type Acute Leukemia

Interventions

  • Drug: Ascentage Pharma HQP1351 bioavailable inhibitor
  • Drug: Blinatumomab — also filed as Blincyto

Primary outcomes

what the primary-completion date above is the date OF
Maximum Plasma Concentration (Cmax) of HQP1351
measured 28 days
Area Under the Curve (AUC) of HQP1351
measured 28 days

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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