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.

NCT05095441

A Clinical Study of Intratumoral MVR-C5252 (C5252) in Patients With Recurrent or Progressive Glioblastoma

UNKNOWN
PHASE1Ages 18+InterventionalTreatment
ImmVira Pharma Co. Ltd
~51 participants
Updated 2022-10-12 on ClinicalTrials.gov
What's tested:C5252

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Evaluate the safety and tolerability of C5252
Measured over Up to 28 days from C5252 injection
+2 more outcomes measured
Solid Tumor
Glioblastoma
Glioblastoma Multiforme
Glioblastoma Multiforme of Brain
1 sites across 1 states
Utah1

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  • 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