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Study of ABT-199 (GDC-0199) in Combination With Azacitidine or Decitabine (Chemo Combo) in Subjects With Acute Myelogenous Leukemia (AML)

Terminated · Phase 1 · NCT02203773

Conditions: Acute Myelogenous Leukemia, Myelogenous Leukemia, Treatment Naive AML

At a glance

Research payments reported, 2025
$160,500
U.S. investigators named
1
Sites paid
2
Planned or actual enrollment
212

About the trial

Sponsor
AbbVie (with Genentech, Inc.)
Tested
Posaconazole (drug), ABT-199 (drug), Decitabine (drug), Azacitidine (drug)
Dates
Started 2014-10-06; completion 2022-06-16
Results posted
Not yet

This is a Phase 1b, open-label, non-randomized, multicenter study to evaluate the safety and pharmacokinetics of orally administered venetoclax (ABT-199) combined with decitabine or azacitidine and the preliminary efficacy of these combinations. In addition, there is a drug-drug interaction (DDI) sub-study only at a single site, to assess the pharmacokinetics and safety of venetoclax (ABT-199) in combination with posaconazole.

From ClinicalTrials.gov, last updated 2023-05-16. Full record, eligibility and contacts (opens in a new tab)

Industry funding

AbbVie Inc. reported $160,500 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

  • Baylor College of Medicin $80,250
  • Baylor College of Medicine $80,250

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