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Study details
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Ivosidenib, Venetoclax, and Azacitidine for Hematologic Malignancies

M.D. Anderson Cancer Center
NCT IDNCT03471260ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1/2

Target enrollment

96

Study length

about 9.5 years

Ages

18+

Locations

4 sites in MA, OH, OR +1

What this study is about

This trial is testing the safety and best dose of venetoclax when combined with ivosidenib and/or azacitidine in treating patients with IDH1-mutated hematologic malignancies. The goal is to determine if this combination treatment works better than venetoclax alone.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Azacitidine
  • 2.Take Ivosidenib
  • 3.Take Venetoclax

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IVsubcutaneous

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

azacitidine, ivosidenib, venetoclax

Drug routes

injection, subcutaneous, oral (Oral Tablet), oral

Endpoints

Primary: Dose-limiting toxicity, Incidence of adverse events, Overall response rate (ORR)

Secondary: Duration of response, Event-free survival, Overall survival

Body systems

Oncology