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A Study of Ponatinib Versus Imatinib in Adults With Acute Lymphoblastic Leukemia

Active, not recruiting · Phase 3 · NCT03589326

Conditions: Philadelphia Chromosome Positive Acute Lymphoblastic Leukemia (Ph+ALL)

At a glance

Research payments reported, 2025
$679,384
U.S. investigators named
12
Sites paid
12
Planned or actual enrollment
245

About the trial

Sponsor
Takeda
Tested
Ponatinib (drug), Imatinib (drug), Vincristine (drug), Dexamethasone (drug), Cytarabine (drug), Methotrexate (drug), Prednisone (drug)
Dates
Started 2018-10-04; completion 2027-07-31
Results posted
Yes

In this study, adults with newly-diagnosed Philadelphia Chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) will receive first-line therapy of ponatinib or imatinib. The main aim of this study is to compare the number of participants on each treatment that show no signs of disease. Participants will take tablets of either ponatinib or imatinib at the same time each day combined with reduced-intensity chemotherapy for up to 20 months. Then, they will continue with single-agent therapy (ponatinib or imatinib) until they meet the discontinuation criteria from the study.

From ClinicalTrials.gov, last updated 2025-11-26. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Takeda Pharmaceuticals U.S.A., Inc. reported $679,384 in research payments for this study in 2025 (98 payments).

Products named: Iclusig

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.