Oncolytic Virus Plus PD-1 Inhibitor to Patients With Advanced Pancreatic Cancer
- Sponsor
- Fudan University
- Study ID
- NCT06196671
- Phase
- PHASE2
- Status
- Not Yet Recruiting
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Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- H101 — DRUGH101 15x10\^11vp intratumorally injection starts at day 1.
- Camrelizumab — DRUGCamrelizumab will be administered at 200 mg i.v. every 3 weeks at day 2.
Study Details
The purpose of this study is to evaluate the efficacy of oncolytic virus plus PD-1 inhibitor to Patients with Advanced Pancreatic Cancer.
Key Dates
- Start date
- Dec 1, 2026
- Status verified
- Mar 2025
- Primary completion
- Jan 1, 2028
- Completion
- Jan 1, 2028
Study Design
- Enrollment
- 30 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Oncolytic virus plus PD-1 inhibitor* H101 intratumorally injection starts at day 1. * Camrelizumab will be administered at 200 mg i.v. every 3 weeks at day 2. * After two cycles of treatment, Camrelizumab will be administered alone at 200 mg i.v. every 3 weeks from cycle 3 until documented disease progression, development of unacceptable toxicity, participant request, or withdrawal of consent. * The following treatment will be applied according to the newest edition of National Comprehensive Cancer Network (NCCN) guideline.
Primary Outcome Measure
Overall survival,OS [ Time Frame: At the end of Cycle 1 (each cycle is 21 days) ]
Central Contacts
- Ying Yang, MD86 64175590
- Guopei Luo, MD
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