Phase 1 Study of C5252 for Recurrent Glioblastoma
This study is testing a new treatment called C5252 for people with glioblastoma, a type of brain tumor, that has come back or gotten worse after previous treatments. C5252 is given as a single injection directly into the tumor. The main goals of this Phase 1 study are to find out if C5252 is safe, what side effects it might cause, and to determine the highest dose that can be given safely. The study plans to enroll about 51 participants. Currently, the study's recruitment status is unclear.
- Study design
- This is a Phase 1, open-label study, meaning both you and your doctors will know which treatment you are receiving. It will enroll approximately 51 participants to evaluate escalating doses of C5252.
- What's involved
- You would receive a single injection of C5252 directly into your tumor on Day 1. The study will then monitor your safety and tolerability for up to 28 days after the injection.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your safety and tolerability will be evaluated for up to 28 days from the C5252 injection.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
A Clinical Study of Intratumoral MVR-C5252 (C5252) in Patients With Recurrent or Progressive Glioblastoma
At a glance
Conditions
Where it's being run
1 sites across 1 statesWho to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- Evaluate the safety and tolerability of C5252Up to 28 days from C5252 injection
Number of participants in dose escalating cohorts with dose limiting toxicities (DLTs), treatment-emergent adverse events (TEAEs), and/or changes in clinical laboratory abnormalities.
- Characterize Dose Limiting ToxicitiesUp to 28 days from C5252 injection
Incidence of DLTs
- Identify the maximum tolerated dose (MTD) and/or the RD of C5252Up to 28 days from C5252 injection
Incidence of DLTs