Clinical Trial of the Safety and Efficacy of IBA Proton Therapy System PROTEUS® PLUS (Hebei)
Condition(s) studied
Investigational drug(s) / intervention(s)
Proton Beam Therapy (PBT): PROTEUS® PLUS
Study summary
This trial will enroll 47 subjects who will be be treated with the IBA PROTEUS® PLUS Proton Beam radiation Therapy (PBT) medical device.
The trial aims to assess the safety and efficacy of PROTEUS® PLUS for radiation therapy to oncology patients, and to provide a clinical basis for product registration application.
Eligibility
Primary outcome measure(s)
- Short term efficacy evaluation — 90 days after the treatment completion
Disease Control Rate (DCR) according to Response Evaluation Criteria in Solid Tumors RECIST Version 1.1 (RECIST 1.1) criteria - Short term safety evaluation — 90 days after the treatment completion
Toxicity of grade 3, 4 and 5 according to CTCAE
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Hebei Yizhou Cancer Hospital | Zhuozhou | Hebei |
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Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07137195 on ClinicalTrials.gov ↗ ← All trials in China