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NCT07243340

A Phase I/IIa Study of C5252 in Patients With Intracranial Tumor

Not yet recruiting Phase 1, PHASE2 Last updated 21 November 2025
What this trial tests

Phase 1, PHASE2 trial testing Herpes Virus C5252 Injection in Glioma, Malignant in 36 participants. Not yet recruiting.

Timeline
15 December 2025
Primary endpoint
15 December 2027
15 December 2028

Quick facts

Lead sponsorImmVira Pharma Co. Ltd
PhasePhase 1, PHASE2
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment36
Start date15 December 2025
Primary completion15 December 2027
Estimated completion15 December 2028
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

ImmVira Pharma Co. Ltd — full company profile →

Who can join

18 and older, any sex, with Glioma, Malignant. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study includes phase I dose escalation part and phase IIa dose expansion part. The goal of this clinical trial is to learn if C5252 treatment is safe and well tolerated in patients with intracranial tumor and to learn preliminary efficacy of C5252. In this study, participants will be given single or multiple doses of C5252 according to protocol followed by toxicity observation, safety follow-up and long-term follow-up.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Glioma, Malignant

Currently open trials in the same condition.

Other ImmVira Pharma Co. Ltd trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07243340.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing