Can engineered immune cells outsmart Hard-to-Treat blood cancers?
NCT ID NCT05457010
First seen Aug 11, 2026 · Last updated Aug 12, 2026 · Updated 1 time
Summary
This early-stage trial is testing an experimental cell therapy for people with acute myeloid leukemia (AML) or high-risk myelodysplastic syndrome (MDS) that has returned or not responded to standard treatments. The therapy uses a patient's own immune cells, modified to recognize a specific protein on cancer cells, along with a targeting molecule that helps them bind and attack. The main goals are to assess safety, find the right dose, and see if the treatment shows any signs of fighting the cancer.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- A combination of genetically modified immune cells (ARC-T cells) and a targeting protein (SPRX002) that helps these cells find and attack cancer cells.
- What this could lead to
- If successful, this could lead to a new treatment option for people with hard-to-treat blood cancers, potentially offering a path to remission.
- What could go wrong
- This is an early-phase trial with a small number of participants, so safety and effectiveness are not yet proven. There are risks of side effects, including severe immune reactions.
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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City of Hope
Duarte, California, 91010, United States
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Dana Farber Cancer Institute
Boston, Massachusetts, 02215, United States
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MD Anderson Cancer Center
Houston, Texas, 77030, United States
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Montefiore Einstein Cancer Center
New Rochelle, New York, 10801, United States
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The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Baltimore, Maryland, 21205, United States
More trials for these conditions
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