ClinicalTrials.gov record
Completed Phase 1 Interventional

IO-202 as Monotherapy and IO-202 Plus Azacitidine ± Venetoclax in Patients in AML and CMML

ClinicalTrials.gov ID: NCT04372433

Public ClinicalTrials.gov record NCT04372433. 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 May 17, 2026, 1:35 PM 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, Multicenter, Open-Label, Dose-Escalation and Expansion, Safety, Pharmacokinetic, Pharmacodynamic, and Clinical Activity Study of Intravenously Administered IO-202 and IO-202 + Azacitidine ± Venetoclax in Acute Myeloid Leukemia (AML) Patients With Monocytic Differentiation and in Chronic Myelomonocytic Leukemia (CMML) Patients

Study identification

NCT ID
NCT04372433
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Immune-Onc Therapeutics
Industry
Enrollment
67 participants

Conditions and interventions

Interventions

  • IO-202 Biological
  • IO-202 and Azacitidine Biological
  • IO-202 and Azacitidine + Venetoclax Biological

Biological

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
Sep 13, 2020
Primary completion
Jan 30, 2025
Completion
Jan 30, 2025
Last update posted
Feb 13, 2025

2020 – 2025

United States locations

U.S. sites
14
U.S. states
8
U.S. cities
14
Facility City State ZIP Site status
University California, Davis (117) Davis California 95817
City of Hope (106) Duarte California 91010
University of California, Irvine (107) Irvine California 92868
UCLA, Medical Center Division of Hematology/Oncology (119) Los Angeles California 90095
Stanford University (114) Palo Alto California 94305
University of California, San Francisco (118) San Francisco California 94143
University of Colorado, Anschutz Medical Campus (103) Aurora Colorado 80045
Winship Cancer Institute of Emory University (105) Atlanta Georgia 30322
The University of Chicago (113) Chicago Illinois 60637
Weill Cornell Medical College, New York Presbyterian Hospital (110) New York New York 10021
Cleveland Clinic, Taussig Cancer Institute (111) Cleveland Ohio 44195
Oregon Health and Science University, Center for Hematologic Malignancies (116) Portland Oregon 97239
University of Texas Southwestern, Simmons Comprehensive Cancer Center (104) Dallas Texas 75390
MD Anderson Cancer Center (101) Houston Texas 77030

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 NCT04372433, 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 Feb 13, 2025 · Synced May 17, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04372433 live on ClinicalTrials.gov.

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