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Study of IMGN632 in Patients With Untreated BPDCN and Relapsed/Refractory BPDCN

Active, not recruiting · Phase 1, Phase 2 · NCT03386513

Conditions: Blastic Plasmacytoid Dendritic Cell Neoplasm, Myeloproliferative Neoplasm

At a glance

Research payments reported, 2025
$181,832
U.S. investigators named
6
Sites paid
6
Planned or actual enrollment
179

About the trial

Sponsor
AbbVie
Tested
IMGN632 (drug)
Dates
Started 2018-01-02; completion 2026-12-30
Results posted
Yes

This is an open-label, multi-center, Phase 1/2 study to determine the MTD and assess the safety, tolerability, PK, immunogenicity, and anti-leukemia activity of IMGN632 when administered as monotherapy to patients with CD123+ disease.

From ClinicalTrials.gov, last updated 2026-09-04. Full record, eligibility and contacts (opens in a new tab)

Industry funding

AbbVie Inc. reported $181,832 in research payments for this study in 2025 (30 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

  • Moffitt Cancer Center $101,240
  • Banner Casa Grande Medical Center, AZ $50,764
  • City of Hope National Medical Ctr $24,830
  • Fred Hutchinson Cancer Research Ctr $3,318
  • Dana-Farber Cancer Institute $840
  • Cll Global Research Foundation $840

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