Clinical Trials in the USA / NCT07417774
Enrolling by invitation
Observational
Liquid Biopsy in Glioblastoma Treated With Chemoradiation and an Oxygen Therapeutic
NCT07417774 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Glioblastoma (GBM)
Study summary
The goal of this sub-study of the RESTORE trial is to identify biomarkers associated with tumor hypoxia, identify biomarkers that differentiate pseudoprogression from true progression, and correlate biomarkers with clinical outcomes.
Eligibility
Inclusion Criteria:
* Subjects must be enrolled in the RESTORE study (NCT03862430) and provide written informed consent for the RESTORE LB sub-study
Primary outcome measure(s)
- Tumor hypoxia biomarkers — until disease progression and up to 5 years
Identify differentially expressed tumor hypoxia markers in newly-diagnosed glioblastoma subjects treated with NanO2 versus placebo in the RESTORE study.
Trial sites (4)
| Facility | City | Region | Status |
|---|---|---|---|
| Center for Neurosciences | Tucson | Arizona | |
| Yale Cancer Center | New Haven | Connecticut | |
| Saint Luke's Cancer Institute | Kansas City | Missouri | |
| Duke University Medical Center | Durham | North Carolina |
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Official registry record
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 NCT07417774 on ClinicalTrials.gov ↗ ← All trials in the USA