Gene-Edited cells take aim at incurable blood diseases
NCT ID NCT07549698
First seen May 02, 2026 · Last updated May 16, 2026 · Updated 2 times
Summary
This early-stage trial tests a new treatment called CTX112 for adults with two serious autoimmune blood diseases—immune thrombocytopenia (ITP) and warm autoimmune hemolytic anemia (wAIHA)—that have not responded to standard therapies. CTX112 uses CRISPR gene editing to create donor T cells that target and destroy faulty immune cells causing the disease. The study will enroll 60 participants to check safety and see if the treatment can control these conditions.
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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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Conditions
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