drugset / Trial / NCT07492706

Safety, Tolerability and Immunogenicity of a Maternal Respiratory Syncytial Virus (RSV) Vaccine (MKK900) in Healthy Adult Women

NCT07492706

Phase 1 Not yet recruiting 120 enrolled MAXVAX Biotechnology Limited Liability Company
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A Phase 1 study to evaluate safety, tolerability and immunogenicity a RSV vaccine in healthy women 18 to 49 years of age

Timeline

Start
2026-04-01
Primary completion
2026-04-30
Completion
2027-01-15

Drugs

EvaluationDrugModalityDoseRoute
Subject MKK900 Unknown 60 ug Intramuscular
Subject MKK900 Unknown 120 ug Intramuscular
Comparator RSVpreF Vaccine 120 ug Intramuscular