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Efficacy, Safety, and Dose-response of a Live Biotherapeutic Product in Women With Acute Vaginal Infection — ELINA  

Bacterial Vaginosis Clinical Trial

Official title:
Efficacy, Safety, and Dose-response of a Live Biotherapeutic Product (BGY-1601-VT) as a First-line Monotherapy in Women With Acute Vaginal Infection: a Randomized, Double-blind, Placebo-controlled Study

Clinical Trial Summary

The purpose of this clinical trial is to investigate the clinical efficacy and safety of a Live Biotherapeutic Product (BGY-1601-VT) intended as a first line of treatment in cases of acute vaginal infection without upfront microbiological confirmed diagnosis

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06450990
Study type Interventional
Source NEXBIOME THERAPEUTICS
Contact Marine CARDONA
Email contact@nexbiome.com
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date July 8, 2024
Completion date February 26, 2026
View Details
See also
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