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Safety of Chlamydia Vaccine CTH522 in Healthy Women Aged 18 to 45 Years

Chlamydia Trachomatis Clinical Trial

Official title:
A Phase I First in Human, Double-blind, Parallel, Randomised and Placebo Controlled Clinical Trial of the Safety of SSI's Adjuvanted Chlamydia Vaccine CTH522 in Healthy Women Aged 18 to 45 Years

Clinical Trial Summary

The present trial is a phase I first in human, double blind, parallel and placebo controlled trial of SSI's adjuvanted chlamydia vaccine CTH522: CTH522-CAF01 (CAF01 is an adjuvant system) and CTH522-Al(OH)3. The trial will be conducted at Imperial College Research site in the United Kingdom.

Subjects are randomly assigned to one of the following three treatment groups in a ratio of 3:3:1.

This trial consisted of 10 visits and 5 telephonic interviews

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02787109
Study type Interventional
Source Statens Serum Institut
Contact
Status Completed
Phase Phase 1
Start date July 2016
Completion date July 31, 2017
View Details
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