Last updated on June 2019

A Study to Evaluate the Efficacy and Safety of Gefapixant (MK-7264) in Women With Endometriosis-Related Pain (MK-7264-034)


Brief description of study

The purpose of this study is to evaluate the efficacy, safety, and tolerability of gefapixant (MK-7264) in premenopausal female participants with moderate to severe endometriosis-related pain. The primary hypothesis: gefapixant is superior to placebo in reducing the average daily pelvic pain score (cyclic and non-cyclic) during Treatment Cycle 2.

Clinical Study Identifier: NCT03654326

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Synexus ( Site 0734)

Scottsdale, AZ United States
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KO Clinical Research, LLC ( Site 0723)

Fort Lauderdale, FL United States
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Uromed LLC ( Site 0410)

Smolensk, Russian Federation
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Women clinic 22 ( Site 0400)

St. Petersburg, Russian Federation
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Recruitment Status: Open


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