Brain cancer boost: radioactive tile added to standard therapy in new trial
NCT ID NCT05342883
First seen Jun 25, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study tests whether adding a special radiation tile (GammaTile) during brain surgery, followed by standard chemotherapy and radiation, is safe and feasible for people with newly diagnosed glioblastoma. About 61 participants will receive the tile implant at the time of tumor removal, then start standard chemoradiation within 21–35 days. The goal is to see if this combination can improve local tumor control without delaying standard treatment.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- GammaTile (cesium-131 brachytherapy device) and temozolomide
- What this could lead to
- If successful, this approach could improve local control of glioblastoma and potentially extend survival when added to standard treatment.
- What could go wrong
- This is a small, single-arm pilot study focused on feasibility and safety, not yet designed to prove efficacy. Adding radiation may increase side effects without clear benefit.
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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Advent Health Orlando
Orlando, Florida, 32803, United States
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Brown University Health
Providence, Rhode Island, 02906, United States
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ECU Health Medical Center - Vidant
Greenville, North Carolina, 27834, United States
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Florida Health Sciences Center, Inc. d/b/a Tampa General Hospital
Tampa, Florida, 33606, United States
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Henry Ford Health System
Detroit, Michigan, 48202, United States
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HonorHeath Scottsdale Osborn Medical Center
Scottsdale, Arizona, 85251, United States
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Indiana University Office of Clinical Research
Indianapolis, Indiana, 46202, United States
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Keck Medicine of USC
Los Angeles, California, 90033, United States
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Kettering Medical Center
Kettering, Ohio, 45429, United States
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Piedmont Healthcare
Atlanta, Georgia, 30309, United States
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RUSH University
Chicago, Illinois, 60607, United States
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St. Louis University Hospital Center
St Louis, Missouri, 63110, United States
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UC Davis Comprehensive Cancer Center
Sacramento, California, 95817, United States
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UTHealth Houston | Memorial Hermann Health System
Houston, Texas, 77030, United States
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University of Kansas Hospital
Kansas City, Kansas, 66016, United States
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University of Minnesota
Minneapolis, Minnesota, 55485, United States
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Other studies related to the condition(s) this trial covers.
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