New drug aims to reduce Blood-Letting in rare blood cancer
NCT ID NCT06985147
First seen Jun 27, 2026 · Last updated Jul 31, 2026 · Updated 1 time
Summary
This study tests an experimental drug called DISC-3405 in 60 adults with polycythemia vera, a condition where the body makes too many red blood cells. The goal is to see if the drug can safely lower the need for phlebotomies (blood removal) and control blood counts. Participants will receive increasing doses of the drug and be monitored for side effects and effectiveness.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Atrium Health - Levine Cancer Center
Charlotte, North Carolina, 28204, United States
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Atrium Health Wake Forest Baptist Medical Center
Winston-Salem, North Carolina, 27157, United States
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Cleveland Clinic
Cleveland, Ohio, 44195, United States
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Duke University
Durham, North Carolina, 27705, United States
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Keck Medicine of USC - Cancer Clinic- Newport Beach
Newport Beach, California, 92663, United States
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MD Anderson Cancer Center
Houston, Texas, 77030, United States
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Mayo Clinic in Arizona
Phoenix, Arizona, 85054, United States
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Mayo Clinic in Florida
Jacksonville, Florida, 32224, United States
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Mayo Clinic in Minnesota
Rochester, Minnesota, 55905, United States
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Ohio State University
Columbus, Ohio, 43210, United States
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Oregon Health & Science University
Portland, Oregon, 97239, United States
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Siteman Cancer Center - Washington University St. Louis
St Louis, Missouri, 63110, United States
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UCLA Health
Los Angeles, California, 90095, United States
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USC Norris Comprehensive Cancer Center
Los Angeles, California, 90033, United States
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University of Washington - Fred Hutchinson Cancer Research Center
Seattle, Washington, 98109, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Massive new study aims to unlock secrets of rare blood cancers
- Blood thickens during exercise in rare disorder, study aims to find why