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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Study Comparing Estradiol Vaginal Inserts 4mcg To IMVEXXY ® (Estradiol Vaginal Inerts 4 mcg) In The Treatment Of Dyspareunia in Women With Vulvur and Vaginal Atrophy

ClinicalTrials.gov ID: NCT05617820

Public ClinicalTrials.gov record NCT05617820. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 1:32 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled, Parallel- Design, Multiple-Site Study to Evaluate the Therapeutic Equivalence of Estradiol Vaginal Inserts 4 mcg (Teva Pharmaceuticals, Inc.) With IMVEXXY® (Estradiol Vaginal Inserts) (TherapeuticsMD, Inc.) in the Treatment of Dyspareunia in Women With Vulvar and Vaginal Atrophy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Randomized, double-blind, placebo-controlled, parallel-designed, multiple-site, bioequivalence study with clinical endpoints.

Study identification

NCT ID
NCT05617820
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Teva Pharmaceuticals USA
Industry
Enrollment
1,050 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
40 Years to 75 Years
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 15, 2022 (Actual)
Primary completion
Mar 15, 2024 (Actual)
Completion
Mar 15, 2024 (Actual)
Last update posted
Sep 30, 2026

2022 – 2024

United States locations

U.S. sites
42
U.S. states
18
U.S. cities
39
Facility City State ZIP Site status
Site 10112 Birmingham Alabama 35218 —
Site 10146 Chandler Arizona 85224 —
Site 10103 Sacramento California 95821 —
Site 10124 Sacramento California 95821 —
Site 10135 San Diego California 92111 —
Site 10136 Milford Connecticut 06460 —
Site 10130 Edgewater Florida 32132 —
Site 10123 Hialeah Florida 33351 —
Site 10139 Lake Worth Florida 33461 —
Site 10115 Leesburg Florida 34748 —
Site 10138 Maitland Florida 32751 —
Site 10107 Miami Lakes Florida 33014 —
Site 10144 Miami Lakes Florida 33014 —
Site 10101 Miami Springs Florida 33166 —
Site 10106 New Port Richey Florida 34652 —
Site 10143 Oldsmar Florida 34677 —
Site 10129 Ormond Beach Florida 32174 —
Site 10116 Palm Harbor Florida 34684 —
Site 10117 Sarasota Florida 34239 —
Site 10121 Sunrise Florida 33351 —
Site 10140 Tampa Florida 33614 —
Site 10119 West Palm Beach Florida 33409 —
Site 10113 Norcross Georgia 30093 —
Site 10104 Wichita Kansas 67226 —
Site 10128 Marrero Louisiana 70072 —
Site 10109 Metairie Louisiana 70001 —
Site 10122 New Orleans Louisiana 70127 —
Site 10105 Saginaw Michigan 95821 —
Site 10111 Las Vegas Nevada 89128 —
Site 10147 North Las Vegas Nevada 89030 —
Site 10126 Lawrenceville New Jersey 08648 —
Site 10137 New Bern North Carolina 28562 —
Site 10145 New Bern North Carolina 28562 —
Site 10134 Philadelphia Pennsylvania 19114 —
Site 10102 Upper Saint Clair Pennsylvania 15241 —
Site 10110 North Charleston South Carolina 29405 —
Site 10118 Chattanooga Tennessee 37404 —
Site 10142 Beaumont Texas 77701 —
Site 10120 Fort Worth Texas 76104 —
Site 10141 Houston Texas 77022 —
Site 10108 Norfolk Virginia 23502 —
Site 10154 Seattle Washington 98105 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05617820, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 30, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05617820 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →