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Active, not recruiting Phase 1Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT03386513

Public ClinicalTrials.gov record NCT03386513. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 12:30 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1/2, Multi-center, Open-label Study of IMGN632 Monotherapy Administered Intravenously in Patients With CD123-positive Acute Myeloid Leukemia and Other CD123-positive Hematologic Malignancies

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT03386513
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
AbbVie
Industry
Enrollment
179 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 2, 2018 (Actual)
Primary completion
Oct 2, 2024 (Actual)
Completion
Dec 30, 2026 (Estimated)
Last update posted
Sep 4, 2026

2018 – 2026

United States locations

U.S. sites
16
U.S. states
10
U.S. cities
16
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294 —
Banner Health MD Anderson Cancer Center Gilbert Arizona 85234 —
City of Hope Medical Center Duarte California 91010 —
UCLA Los Angeles California 90095 —
Stanford Stanford California 94305 —
Moffitt Cancer Center Tampa Florida 33612 —
University of Maryland Medical Center Baltimore Maryland 21201 —
Dana-Farber Cancer Institute Boston Massachusetts 02215 —
Roswell Park Cancer Institute Buffalo New York 14263 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
Novant Health Cancer Institute Hematology Charlotte North Carolina 28204 —
Duke Cancer Institute Durham North Carolina 27710 —
Novant Health Cancer Institute Hematology - Forsyth Winston-Salem North Carolina 27103 —
Baylor Scott & White University Medical Center Dallas Texas 75246 —
MD Anderson Cancer Center Houston Texas 77030-7095 —
Fred Hutchinson Cancer Research Center/Seattle Cancer Care Alliance Seattle Washington 98109 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 13 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03386513, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 4, 2026 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03386513 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →