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Completed Phase 2 Interventional Results available

Bay98-7196, Dose Finding / POC Study

ClinicalTrials.gov ID: NCT02203331

Public ClinicalTrials.gov record NCT02203331. 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, 8:56 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, Double-dummy, Parallel- Group, Multi-center Phase IIb Study to Assess the Efficacy and Safety of Different Dose Combinations of an Aromatase Inhibitor and a Progestin in an Intravaginal Ring Versus Placebo and Leuprorelin / Leuprolide Acetate in Women With Symptomatic Endometriosis Over a 12-week Treatment Period

Brief summary

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

Purpose of the study is to test efficacy and safety of BAY98-7196 intravaginal ring as a new treatment option for patients with endometriosis-associated pelvic pain

Study identification

NCT ID
NCT02203331
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bayer
Industry
Enrollment
319 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Oct 16, 2014 (Actual)
Primary completion
Oct 24, 2016 (Actual)
Completion
Oct 24, 2016 (Actual)
Last update posted
Nov 7, 2023

2014 – 2016

United States locations

U.S. sites
25
U.S. states
15
U.S. cities
25
Facility City State ZIP Site status
Not listed San Diego California 92108 —
Not listed San Francisco California 94158-2509 —
Not listed Gainesville Florida 32605 —
Not listed New Port Richey Florida 34652 —
Not listed Atlanta Georgia 30338 —
Not listed Sandy Springs Georgia 30328 —
Not listed Chicago Illinois 60611 —
Not listed Palos Heights Illinois 60463 —
Not listed Wichita Kansas 67226 —
Not listed Marrero Louisiana 70072 —
Not listed Canton Michigan 48187 —
Not listed Detroit Michigan 48034 —
Not listed Saginaw Michigan 48604 —
Not listed Lincoln Nebraska 68510 —
Not listed Neptune City New Jersey 07754 —
Not listed Plainsboro New Jersey 08536 —
Not listed Durham North Carolina 27713 —
Not listed Greensboro North Carolina 27408 —
Not listed Winston-Salem North Carolina 27103 —
Not listed Columbus Ohio 43213 —
Not listed Dayton Ohio 45409 —
Not listed Philadelphia Pennsylvania 19104 —
Not listed Chattanooga Tennessee 37404 —
Not listed Seattle Washington 98105 —
Not listed Madison Wisconsin 53562 —

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 92 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02203331, 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 Nov 7, 2023 · Synced Oct 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02203331 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →