drugset / Trial / NCT06337643

A Study to Evaluate Tolerability, Safety and Immunogenicity of MVX01 Pneumococcal Vaccine

NCT06337643 ↗

Phase 1 Unknown 75 enrolled Matrivax Research and Development Corporation
RandomizedSequentialTriple-blindPrevention

Summary

The objectives of this first-in-human study is to evaluate the tolerability, safety, and immunogenicity of MVX01, a pneumococcal vaccine candidate, at four dose levels.

Timeline

Start
2023-03-07
Primary completion
2024-04-16
Completion
2024-04-16

Drugs

EvaluationDrugModalityDoseRoute
Subject MVX01 Vaccine 10 ug Intramuscular
Subject MVX01 Vaccine 30 ug Intramuscular
Subject MVX01 Vaccine 60 ug Intramuscular
Subject MVX01 Vaccine 90 ug Intramuscular

Indications

No indication recorded.