New drug combo aims to boost platelets in Hard-to-Treat ITP
NCT ID NCT07362199
First seen Jan 24, 2026 · Last updated Jun 22, 2026 · Updated 21 times
Summary
This phase 2 trial tests whether combining rituximab with daratumumab can raise platelet counts in adults with immune thrombocytopenia (ITP) who have not responded to steroids. Twenty participants will receive one dose of rituximab and eight doses of daratumumab over eight weeks. The main goal is to see how many achieve a partial or complete response by week 12.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Study contacts
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Contact
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Contact
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Locations
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Chinese Academy of Medical Science and Blood Disease Hospital
RECRUITINGTianjin, Tianjin Municipality, 300020, China
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Contact
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What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
Active substance
rituximab combined with daratumumab (anti-CD38 monoclonal antibody)
What this could lead to
If successful, this combination could offer a new treatment option for people with immune thrombocytopenia who have not responded to steroids.
What could go wrong
This is a small, early-phase trial with only 20 participants, so results may not apply to everyone. The combination may cause side effects or fail to improve platelet counts.
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.