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NCT02203331 · ClinicalTrials.gov registry record · Phase 2

Bay98-7196, Dose Finding / POC Study

A Phase 2 study, sponsored by Bayer.

Completed
Registry status
Phase 2
Development phase
319
Enrollment target

NCT02203331: Completed Phase 2 study, sponsored by Bayer.

NCT02203331 is a Phase 2 study that has completed, run by Bayer. The registered enrollment target is 319 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (140% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02203331, a Phase 2 study, has completed, sponsored by Bayer.

COMPLETED
Registry status
Phase 2
Development phase
319 participants
Enrollment target

Study Summary

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

Primary Outcome

Pain intensity was assessed on 11-point (0-10) NRS by question 1. In question 1, participants were asked to rate the pain in the target area during the past 24 hours, where 0= no pain and 10= worst imaginable pain and responses were recorded in ESD. The mean pain of the 7 days with worst EAPP within a 28-day window was calculated as the sum of ESD item 1 on 7 days with worst EAPP within that 28-day window divided by 7.

Interventions

  • DRUG Placebo
  • DRUG Anastrozole
  • DRUG Levonorgestrel
  • DRUG Lupron / Leuprolide acetate

Trial Details

FieldValue
Enrollment Target 319 participants
Start Date 2014-10-16
Est. Completion 2016-10-24
Phase Phase 2
Bayer

591 total trials

What the finished NCT02203331 record still lists

NCT02203331 is an interventional study that assigns participants to a tested intervention. The registered 319 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (140% higher).

The record links to 0 conditions, and to 4 interventions - of which Placebo is the first listed.

NCT02203331 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02203331 about?

NCT02203331 is a clinical study titled "Bay98-7196, Dose Finding / POC Study". 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

What is the current status of trial NCT02203331?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 319 participants. The study started on 2014-10-16. Estimated completion is 2016-10-24.

What interventions are being tested in trial NCT02203331?

The interventions under investigation include: Placebo (DRUG), Anastrozole (DRUG), Levonorgestrel (DRUG), Lupron / Leuprolide acetate (DRUG).

Who is sponsoring clinical trial NCT02203331?

This trial is sponsored by Bayer, which has 591 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02203331's enrollment target sits among peer trials

319 153rd of 2000 higher than 1,848 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02203331, the US trial registry maintained by the National Library of Medicine. NCT02203331 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.