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Terminated Phase 1 Interventional

A Study of Voruciclib Alone or in Combination With Venetoclax in Subjects With B-Cell Malignancies or AML

ClinicalTrials.gov ID: NCT03547115

Public ClinicalTrials.gov record NCT03547115. 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 Nov 2, 2026, 11:57 AM EST

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

Official title

Phase 1, Open-label, Study of Voruciclib in Subjects With Relapsed and/or Refractory B Cell Malignancies or AML After Failure of Prior Standard Therapies and Voruciclib in Combination With Venetoclax in Subjects With Relapsed/Refractory AML

Brief summary

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

This is a Phase 1, open-label, dose escalation study to determine the safety and preliminary efficacy of voruciclib monotherapy in subjects with relapsed/refractory B cell malignancies or AML after failure of standard therapies or voruciclib in combination with venetoclax in subjects with relapsed or refractory AML

Study identification

NCT ID
NCT03547115
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
MEI Pharma, Inc.
Industry
Enrollment
84 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
May 31, 2018 (Actual)
Primary completion
Jul 24, 2024 (Actual)
Completion
Jul 24, 2024 (Actual)
Last update posted
Mar 17, 2026

2018 – 2024

United States locations

U.S. sites
12
U.S. states
12
U.S. cities
12
Facility City State ZIP Site status
City of Hope Duarte California 91010 —
Northwestern Memorial Hospital Chicago Illinois 60611 —
Dana Farber Cancer Institute Boston Massachusetts 02215 —
Mayo Clinic Rochester Minnesota 55905 —
University of Nebraska Medical Center Omaha Nebraska 68198 —
New York University New York New York 10016 —
Duke University Durham North Carolina 27705 —
Oregon Health and Science University Portland Oregon 97239 —
MD Anderson Houston Texas 77030 —
University of Virginia Charlottesville Virginia 22903 —
Swedish Cancer Institute Seattle Washington 98104 —
Froedtert Hospital & the Medical College of Wisconsin 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03547115, 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 17, 2026 · Synced Nov 2, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03547115 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →