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RecruitingNCT06026774

Clinical Study of Personalized mRNA Vaccine Encoding Neoantigen in Subjects With Resected Digestive System Neoplasms

A Clinical Study to Assess the Safety, Feasibility, and Efficacy of Personalized mRNA Vaccine Encoding Neoantigen in Combination With Standard Adjuvant Therapy in Subjects With Resected Digestive System Neoplasms

Status
Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
Sir Run Run Shaw Hospital · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to assess the safety, feasibility, and efficacy of personalized mRNA vaccine iNeo-Vac-R01 with standard adjuvant therapy in subjects with surgically resected digestive system neoplasms.

Detailed description

This is a single-center, open-label, single-arm clinical study of personalized mRNA vaccine iNeo-Vac-R01 in combination with standard adjuvant therapy in subjects with surgically resected digestive system neoplasms.

Conditions

Interventions

TypeNameDescription
BIOLOGICALiNeo-Vac-R01 in combination with standard adjuvant therapyPersonalized mRNA vaccine encoding neoantigen, IH injection

Timeline

Start date
2023-09-08
Primary completion
2027-08-31
Completion
2027-12-31
First posted
2023-09-07
Last updated
2023-09-11

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06026774. Inclusion in this directory is not an endorsement.

Clinical Study of Personalized mRNA Vaccine Encoding Neoantigen in Subjects With Resected Digestive System Neoplasms (NCT06026774) · Clinical Trials Directory