Study of AZD0120 in Newly Diagnosed Multiple Myeloma Ineligible for ASCT (NCT07764978)
Phase III Open-Label, Randomised Study of Consolidation With AZD0120 (Dual-Targeting BCMA/CD19 CAR-T) vs Continuous Standard Therapy in NDMM Patients Ineligible for ASCT as Initial Therapy (DURGA-5)
๐ฉบ Plain-English Summary (8th-Grade Level)
This is a randomised, multicentre, controlled, open-label, Phase III global study comparing the efficacy and safety of standard induction regimens (IsaVRd and DRd) followed by AZD0120 versus standard induction regimens followed by continuous therapy (IsaRd and DRd) in participants with newly diagnosed multiple myeloma (NDMM) who are ineligible for autologous stem cell transplant (ASCT) as initial therapy.
Who can join: Review the eligibility criteria below.
Location: Research Site โ Gilbert, Arizona
Age range: 18 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (124 Sites)
Showing the first 25 of 124 sites.
- Research Site โ Gilbert, Arizona
- Research Site โ Phoenix, Arizona
- Research Site โ Tucson, Arizona
- Research Site โ Orange, California
- Research Site โ Santa Monica, California
- Research Site โ Aurora, Colorado
- Research Site โ Denver, Colorado
- Research Site โ New Haven, Connecticut
- Research Site โ Coral Gables, Florida
- Research Site โ Tampa, Florida
- Research Site โ Atlanta, Georgia
- Research Site โ Chicago, Illinois
- Research Site โ Iowa City, Iowa
- Research Site โ Wichita, Kansas
- Research Site โ Louisville, Kentucky
- Research Site โ Baton Rouge, Louisiana
- Research Site โ Baltimore, Maryland
- Research Site โ Detroit, Michigan
- Research Site โ St Louis, Missouri
- Research Site โ East Brunswick, New Jersey
- Research Site โ Albany, New York
- Research Site โ New Hyde Park, New York
- Research Site โ New York, New York
- Research Site โ New York, New York
- Research Site โ New York, New York
๐ 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.
๐ฐ 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 ยง 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.
More studies in Newly Diagnosed Multiple Myeloma
Explore by condition: All Newly Diagnosed Multiple Myeloma clinical trials
๐ก 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.