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Completed Phase 3 Interventional Accepts healthy volunteers

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 Jul 21, 2026, 10:03 PM 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

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

  • Estradiol Drug
  • Imvexxy Drug
  • Placebo Drug

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 14, 2022
Primary completion
Mar 14, 2024
Completion
Mar 14, 2024
Last update posted
Apr 11, 2024

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 Apr 11, 2024 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05617820 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →