New drug IASO-782 aims to tame immune attacks on blood cells
NCT ID NCT06534021
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This early-stage trial is testing a new drug called IASO-782 in 16 adults with autoimmune thrombocytopenia (ITP) or warm autoimmune hemolytic anemia (wAIHA). These conditions cause the immune system to mistakenly attack blood cells. The study's main goal is to check the drug's safety and how well the body tolerates it. Participants receive a single dose of IASO-782 or a placebo, and researchers will monitor for side effects.
What this could mean
Our plain-language read of the trial. This is informational only โ not medical advice or a prediction.
- Active substance
- IASO-782 injection
- What this could lead to
- If successful, this could point toward a new treatment option for people with autoimmune blood disorders that haven't responded to standard therapies.
- What could go wrong
- This is a very early Phase 1 trial with only 16 participants, so safety and dosing are the main focus. It is too soon to know if IASO-782 will be effective, and there may be unknown side effects.
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
-
Institute of Hematology, Chinese Academy of Medical Sciences
RECRUITINGTianjin, Tianjin Municipality, 300020, China
-
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
RECRUITINGWuhan, Hubei, 430022, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Double attack on blood disorder: could two drugs beat one for stubborn ITP?
- Could a cholesterol drug and antioxidant help treat a rare bleeding disorder?
- New hope for lupus patients with dangerous low platelet counts
- Can a simple blood test predict who will get chronic ITP?
- New pill could help patients with rare blood disorder