drugset / Trial / NCT06442449

Booster Dose of sIPV Co-administered With MMR and HepA-I.

NCT06442449 ↗

Phase 4 Completed 889 enrolled Sinovac Biotech Co., Ltd
RandomizedParallel-groupOpen-labelPrevention

Summary

This is an Open-labeled, Randomized, Controlled Phase IV Clinical Trial to Evaluate the Immunogenicity and Safety of Booster Dose of Sabin Strain Inactivated Poliovirus Vaccine (Vero cell) (sIPV) Co-administered with Measles, Mumps, Rubella (MMR) Combined Live Attenuated Vaccine and Inactivated Hepatitis A (Hep-A) Vaccine.

Timeline

Start
2024-08-08
Primary completion
2025-09-10
Completion
2025-10-10

Outcome

Met primary endpoint

paper all pairwise SCR differences met non-inferiority (-10% margin). PMID 41295459 ↗

paper CONCLUSIONS: Same-day sIPV co-administration with MMRV or HepA was non-inferior and well tolerated, supporting programmatic adoption. PMID 41295459 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject HepA-I Vaccine — —
Subject Measles, Mumps, Rubella (MMR) Combined Live Attenuated Vaccine Vaccine — —
Subject Sabin Strain Inactivated Poliovirus Vaccine (Vero cell) Vaccine — —

Indications