Could a cancer drug tame rare clotting disorder?
NCT ID NCT05671757
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study tests whether daratumumab, a drug used for certain cancers, is safe for people with antiphospholipid syndrome (APS), an autoimmune disorder that raises blood clot risk. Up to 22 adults will receive weekly infusions for 8 weeks at different doses. The main goal is to check for serious side effects during dose escalation.
What this could mean
Our plain-language read of the trial. This is informational only โ not medical advice or a prediction.
- Active substance
- daratumumab (a drug that targets immune cells)
- What this could lead to
- If safe and effective, daratumumab could offer a new treatment option for antiphospholipid syndrome, reducing blood clot risk.
- What could go wrong
- This is a very early, small safety trial (phase 1b/2) with only 22 participants. It may not show benefit, and side effects like infections or allergic reactions are possible.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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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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Duke University
RECRUITINGDurham, North Carolina, 27710, United States
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Hospital for Special Surgery
RECRUITINGNew York, New York, 10021, United States
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Johns Hopkins University
RECRUITINGBaltimore, Maryland, 21205, United States
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Mayo Clinic Rochester
COMPLETEDRochester, Minnesota, 55905, United States
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NYU Langone
RECRUITINGNew York, New York, 10016, United States
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Northwell Health
RECRUITINGGreat Neck, New York, 11021, United States
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University of Michigan
RECRUITINGAnn Arbor, Michigan, 48109, United States
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Weill Cornell
RECRUITINGNew York, New York, 10021, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- New drug aims to tame antibodies in rare clotting disorder
- Promising new treatment for rare Muscle-Weakening disease enters human trials
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