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Not Yet RecruitingNCT07243340

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

A Phase I/IIa Study to Evaluate the Safety, Tolerability, and Preliminary Efficacy of Herpes Virus C5252 Injection in Patients With Intracranial Tumor

Status
Not Yet Recruiting
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
36 (estimated)
Sponsor
ImmVira Pharma Co. Ltd · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
BIOLOGICALHerpes Virus C5252 InjectionC5252 will be administered at designed dose level.

Timeline

Start date
2025-12-15
Primary completion
2027-12-15
Completion
2028-12-15
First posted
2025-11-21
Last updated
2025-11-21

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07243340. Inclusion in this directory is not an endorsement.

A Phase I/IIa Study of C5252 in Patients With Intracranial Tumor (NCT07243340) · Clinical Trials Directory