drugset / Trial / NCT06927297

Phase I Study of the Safety, Tolerability, and Efficacy of an Engineered Mitochondrial Vaccine in Advanced Solid Tumors

NCT06927297 ↗

Phase 1 Recruiting 12 enrolled West China Hospital
NaSequentialOpen-labelTreatment

Summary

This study is a dose-escalation, prospective clinical trial to assess the safety, tolerability, and preliminary therapeutic efficacy of engineered mitochondria expressing specific tumor antigen in patients with advanced solid tumors.

Timeline

Start
2025-05-09
Primary completion
2026-12-31
Completion
2028-04-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Engineered mitochondrial vaccine Vaccine 25 ug Subcutaneous
Subject Engineered mitochondrial vaccine Vaccine 50 ug Subcutaneous
Subject Engineered mitochondrial vaccine Vaccine 100 ug Subcutaneous
Subject Engineered mitochondrial vaccine Vaccine 200 ug Subcutaneous