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Terminated Phase 1 Interventional

Study to Evaluate Adverse Events and Movement of Intravenously (IV) Infused ABBV-787 in Adult Participants With Relapsed/Refractory (R/R) Acute Myeloid Leukemia (AML)

ClinicalTrials.gov ID: NCT06068868

Public ClinicalTrials.gov record NCT06068868. 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 Jul 24, 2026, 12:27 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 First-in-Human Study Evaluating Safety, Pharmacokinetics and Efficacy of ABBV-787 in Adult Subjects With Acute Myeloid Leukemia (AML)

Study identification

NCT ID
NCT06068868
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
AbbVie
Industry
Enrollment
36 participants

Conditions and interventions

Interventions

  • ABBV-787 Drug

Drug

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
Nov 12, 2023
Primary completion
Feb 24, 2025
Completion
Feb 24, 2025
Last update posted
Mar 5, 2025

2023 – 2025

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
City of Hope /ID# 253727 Duarte California 91010
University of California Davis Health /ID# 252723 Sacramento California 95817
Yale University School of Medicine /ID# 252724 New Haven Connecticut 06510
Northwestern Memorial Hospital /ID# 252800 Chicago Illinois 60611-2927
University of Chicago Medical /ID# 252764 Chicago Illinois 60637
University of Maryland, Baltimore /ID# 253726 Baltimore Maryland 21201
Cancer & Hematology Centers /ID# 252803 Grand Rapids Michigan 49503
Memorial Sloan Kettering Cancer Center-Koch Center /ID# 252515 New York New York 10065-6007
Weill Cornell Medical College /ID# 252516 New York New York 10065
University of Pennsylvania /ID# 252789 Philadelphia Pennsylvania 19104-5502
St. David's South Austin Medical Center /ID# 252790 Austin Texas 78704
MD Anderson Cancer Center /ID# 252514 Houston Texas 77030
Fred Hutchinson Cancer Research Center /ID# 253730 Seattle Washington 98109-1024
Wisconsin Medical Center /ID# 252513 Milwaukee Wisconsin 53226

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 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06068868, 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 Mar 5, 2025 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06068868 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →