Study of AZD3632 Monotherapy or in Combination With Anticancer Agents in Participants With Advanced Haematologic Malignancies With KMT2Ar, NPM1m, or Other Genotypes Associated With HOX Overexpression (NCT07155226)
A Modular Phase I/II, Open-label, Multi-Centre Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy of AZD3632 Monotherapy or in Combination With Anticancer Agents in Participants With Advanced Haematologic Malignancies With KMT2Ar, NPM1m, or Other Genotypes Associated With HOX Overexpression
🩺 Plain-English Summary (8th-Grade Level)
The purpose of this study is to understand the safety, tolerability, efficacy, pharmacokinetic (PK), pharmacodynamic (PD), and preliminary efficacy of orally administered AZD3632 in participants with advanced haematologic malignancies with KMT2Ar, NPM1m, or other genotypes associated with homeobox (HOX) overexpression.
Who can join: Review the eligibility criteria below.
Location: Research Site — Decatur, Illinois
Age range: 16 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (30 Sites)
Showing the first 25 of 30 sites.
- Research Site — Decatur, Illinois
- Research Site — New York, New York
- Research Site — Chapel Hill, North Carolina
- Research Site — Durham, North Carolina
- Research Site — Portland, Oregon
- Research Site — Houston, Texas
- Research Site — Fitzroy,
- Research Site — Perth,
- Research Site — Toronto, Ontario
- Research Site — Montreal, Quebec
- Research Site — Copenhagen,
- Research Site — Dresden,
- Research Site — Frankfurt A. Main,
- Research Site — Halle,
- Research Site — Heidelberg,
- Research Site — München,
- Research Site — Ulm,
- Research Site — Bologna,
- Research Site — Ravenna,
- Research Site — Bunkyō City,
- Research Site — Kashiwa,
- Research Site — Okayama,
- Research Site — Seoul,
- Research Site — Seoul,
- Research Site — Seoul,
📞 Contact the Study Coordinator
Phone: (877) 240-9479
Email: information.center@astrazeneca.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.