drugset / Trial / NCT04921111

A Phase I Safty and Immunogenicity Study of SCT1000 in Healthy Women Aged 18 to 45 Years

NCT04921111

Phase 1 Unknown 240 enrolled Sinocelltech Ltd.
RandomizedParallel-groupDouble-blindPrevention

Summary

A phase 1 random, double blind, positive and placebo control trail was conducted in 120 healthy women in the arm A: 18-26 years old and Arm B: 27-45 years old. The 40 subjects to be inoculated with low, middle, and high dose vaccinefirst in sequence if there was no safety issue. In each dose group SCT1000 : placebo: positive =3:1:1.Two arms can be recruited at the same time. If the DSMB assessment shows that the adverse events of a certain dose group meet the criteria of suspension / termination, the dose group will be suspended / terminated, and the vaccination of this dose group or higher dose group will not be carried out, and the study of other dose groups will continue. If this happens at a low dose, the study will be suspended / terminated.

Timeline

Start
2021-07-02
Primary completion
2022-07-31
Completion
2022-10-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Gardasil Vaccine
Subject Gardasil 9 Vaccine
Subject SCT1000 Vaccine

Indications

No indication recorded.