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IMGN632 as Monotherapy or With Venetoclax and/or Azacitidine for Participants With CD123-Positive Acute Myeloid Leukemia

Active, not recruiting · Phase 1, Phase 2 · NCT04086264

Conditions: Acute Myeloid Leukemia

At a glance

Research payments reported, 2025
$575,040
U.S. investigators named
8
Sites paid
8
Planned or actual enrollment
218

About the trial

Sponsor
AbbVie
Tested
Azacitidine (drug), IMGN632 (drug), Venetoclax (drug)
Dates
Started 2019-11-06; completion 2027-02
Results posted
Not yet

This is an open-label, multicenter, Phase 1b/2 study to determine the safety and tolerability of IMGN632 and assess the antileukemia activity of IMGN632 when administered in combination with azacitidine and/or venetoclax in participants with relapsed and frontline CD123-positive AML.

From ClinicalTrials.gov, last updated 2025-08-14. Full record, eligibility and contacts (opens in a new tab)

Industry funding

AbbVie Inc. reported $575,040 in research payments for this study in 2025 (53 payments).

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.