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Study identifier: NCT04260022 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Leukemia, Myeloid, Chronic · Myeloid Leukemia · Chronic Myeloid Leukemia  ·  Sponsor: Ascentage Pharma Group Inc.

PhasePhase 1
Planned participants242
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

A multi-center, open-label, randomized, phase Ib study to evaluate the pharmacokinetics (PK) of HQP1351 and to determine the recommended phase 2 dose (RP2D) of HQP1351 in subjects with CML chronic phase (CP), accelerated phase (AP), or blast phase (BP) or with Ph+ ALL, who have experienced resistance or intolerance to at least two tyrosine kinase inhibitors (TKIs) or in subjects with Ph+ B-cell precursor (BCP) ALL or lymphoid blast phase CML (CML LBP), who have experienced resistance or intolerance to at least one second or later generation TKI.

This description comes directly from the study's public registry record.

Talk to the study team

Bill Garrett  ·  301-520-3962  ·  Bill.Garrett@ascentage.com

Always discuss trial participation with your own doctor first.

Locations (9)

University of Alabama at BirminghamBirmingham, Alabama, United StatesRecruiting
City of HopeDuarte, California, United StatesRecruiting
Winship Cancer Institute, Emory UniversityAtlanta, Georgia, United StatesRecruiting
Augusta Cancer CenterAugusta, Georgia, United StatesRecruiting
University of MarylandBaltimore, Maryland, United StatesRecruiting
Cleveland ClinicCleveland, Ohio, United StatesRecruiting
University of Texas MD Anderson Cancer CenterHouston, Texas, United StatesRecruiting
Fred Hutchinson Cancer Research CenterSeattle, Washington, United StatesRecruiting
Princess Margaret Cancer CentreToronto, Ontario, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT04260022