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Antimicrobial Agent
EVO100 for Gonorrhea (EVOGUARD Trial)
Phase 3
Waitlist Available
Research Sponsored by Evofem Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 16 weeks
Awards & highlights
EVOGUARD Trial Summary
This study is evaluating whether a vaginal gel may help prevent the sexual transmission of certain sexually transmitted infections.
Eligible Conditions
- Gonorrhea
- Chlamydia
- Sexually Transmitted Infections
EVOGUARD Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 16 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~16 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Percentage of Study Successes in the EVO100 and Placebo Treatment Groups
Secondary outcome measures
Evaluate Safety of EVO100: AEs
Side effects data
From 2019 Phase 2 & 3 trial • 860 Patients • NCT031073775%
Vulvovaginal Candidiasis
3%
Bacterial Vaginosis
3%
Urinary tract infections
3%
Vaginal Discharge
2%
Vulvovaginal discomfort
100%
80%
60%
40%
20%
0%
Study treatment Arm
EVO100
Placebo
EVOGUARD Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: EVO100 gelExperimental Treatment1 Intervention
EVO100 vaginal gel, 5 g
Group II: Placebo gelPlacebo Group1 Intervention
Placebo vaginal gel, 5 g
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
EVO100
2017
Completed Phase 3
~2760
Find a Location
Who is running the clinical trial?
Evofem Inc.Lead Sponsor
6 Previous Clinical Trials
6,631 Total Patients Enrolled
Brandi Howard, PhDStudy DirectorEvofem Inc.
Catherine Maher, PhDStudy DirectorEvofem Inc.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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