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A Study of Venetoclax and Dinaciclib (MK7965) in Patients With Relapsed/Refractory Acute Myeloid Leukemia

Terminated · Phase 1 · NCT03484520

Conditions: Cancer - Acute Myeloid Leukemia

At a glance

Research payments reported, 2025
$3,900
U.S. investigators named
1
Sites paid
1
Planned or actual enrollment
48

About the trial

Sponsor
AbbVie (with Merck Sharp & Dohme LLC)
Tested
Venetoclax (drug), Dinaciclib (drug)
Dates
Started 2018-07-23; completion 2022-12-01
Results posted
Not yet

An open-label, dose-escalation study to assess safety, pharmacokinetics and efficacy as well as determine the recommended Phase 2 doses of co-administered therapy of dinaciclib and venetoclax for patients with relapsed or refractory Acute Myeloid Leukemia (R/R AML).

From ClinicalTrials.gov, last updated 2022-12-30. Full record, eligibility and contacts (opens in a new tab)

Industry funding

AbbVie Inc. reported $3,900 in research payments for this study in 2025 (2 payments).

Products named: Venclexta

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

  • University of Chicago $3,900

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