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Completed Phase 1 Interventional

A Study of Venetoclax and Alvocidib in Patients With Relapsed/Refractory Acute Myeloid Leukemia

ClinicalTrials.gov ID: NCT03441555

Public ClinicalTrials.gov record NCT03441555. 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 Sep 27, 2026, 5:55 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

Phase 1b Study of Venetoclax and Alvocidib in Patients With Relapsed/Refractory Acute Myeloid Leukemia

Brief summary

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

An open-label, dose-escalation study to assess the safety and pharmacokinetics (PK), to determine the dose limiting toxicity (DLT) and the recommended Phase 2 dose (RPTD), and to assess the preliminary efficacy of alvocidib with venetoclax when co-administered in participants with relapsed or refractory (R/R) acute myeloid leukemia (AML).

Study identification

NCT ID
NCT03441555
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
AbbVie
Industry
Enrollment
36 participants

Conditions and interventions

Interventions

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
May 29, 2018
Primary completion
Jan 24, 2021
Completion
Jan 24, 2021
Last update posted
Jan 31, 2022

2018 – 2021

United States locations

U.S. sites
9
U.S. states
6
U.S. cities
8
Facility City State ZIP Site status
USC Norris Cancer Center /ID# 170844 Los Angeles California 90033 —
UC Irvine /ID# 201093 Orange California 92868 —
University of California, Davis Comprehensive Cancer Center /ID# 170799 Sacramento California 95817 —
Sylvester Comprehensive Cancer /ID# 170761 Miami Florida 33136-1002 —
Indiana Blood & Marrow Transpl /ID# 170793 Indianapolis Indiana 46237 —
NYU Langone Medical Center /ID# 201559 New York New York 10016-6402 —
Weill Cornell Medical College /ID# 170800 New York New York 10021 —
Duke University Medical Center /ID# 170842 Durham North Carolina 27710-3000 —
University of Pittsburgh Medic /ID# 170790 Pittsburgh Pennsylvania 15261 —

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03441555, 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 Jan 31, 2022 · Synced Sep 27, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03441555 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →