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Completed Phase 2 Interventional Results available

A Study to Assess the Efficacy and Safety of OBE2109 in Subjects With Endometriosis

ClinicalTrials.gov ID: NCT02778399

Public ClinicalTrials.gov record NCT02778399. 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 20, 2026, 3:12 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, Phase 2b Dose-ranging Study to Assess the Efficacy and Safety of OBE2109 in Subjects With Endometriosis Associated Pain

Brief summary

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

The primary objective of this study is to assess the efficacy and safety of a range of oral doses of OBE2109 versus placebo, in reducing endometriosis associated pain.

Study identification

NCT ID
NCT02778399
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
ObsEva SA
Industry
Enrollment
328 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 45 Years
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
Jul 2016 (Actual)
Primary completion
Apr 2018 (Actual)
Completion
Jul 1, 2019 (Actual)
Last update posted
Jul 21, 2022

2016 – 2019

United States locations

U.S. sites
71
U.S. states
24
U.S. cities
62
Facility City State ZIP Site status
Site reference ID 455 Chandler Arizona — —
Site reference ID 439 Scottsdale Arizona — —
Site reference ID 462 Arcadia California — —
Site reference ID 405 Chino California — —
Site reference ID 463 Huntington Park California — —
Site refenrec ID 469 Northridge California — —
Site reference ID 431 San Diego California — —
Site reference ID 440 Tustin California — —
Site reference ID 474 Denver Colorado — —
Site reference ID 450 Lakewood Colorado — —
Site reference ID 425 Longmont Colorado — —
Site reference ID 410 Washington D.C. District of Columbia — —
Site reference ID 457 Boca Raton Florida — —
Site reference ID 418 Clearwater Florida — —
Site reference ID 437 Gainesville Florida — —
Site reference ID 458 Jensen Beach Florida — —
Site reference ID 411 Miami Florida — —
Site reference ID 424 Miami Florida — —
Site reference ID 435 Miami Florida — —
Site reference ID 420 Miami Lakes Florida — —
Site reference ID 441 Miami Springs Florida — —
Site reference ID 423 New Port Richey Florida — —
Site reference ID 426 Tampa Florida — —
Site reference ID 442 Wellington Florida — —
Site reference ID 428 Atlanta Georgia — —
Site reference ID 459 Atlanta Georgia — —
Site reference ID 475 Nampa Idaho — —
Site reference ID 465 Oak Brook Illinois — —
Site reference ID 404 Shawnee Mission Kansas — —
Site reference ID 456 Wichita Kansas — —
Site reference ID 454 Marrero Louisiana — —
Site reference ID 453 Metairie Louisiana — —
Site reference ID 478 Glen Burnie Maryland — —
Site reference ID 445 Fall River Massachusetts — —
Site reference ID 471 Fall River Massachusetts — —
Site reference ID 430 Ann Arbor Michigan — —
Site reference ID 409 Bay City Michigan — —
Site reference ID 468 Saginaw Michigan — —
Site reference ID 473 Saginaw Michigan — —
Site reference ID 427 Southfield Michigan — —
Site reference ID 421 Albuquerque New Mexico — —
Site reference ID 466 New York New York — —
Site reference ID 436 Greensboro North Carolina — —
Site reference ID 433 Morehead City North Carolina — —
Site reference ID 443 Dayton Ohio — —
Site reference ID 472 Franklin Ohio — —
Site reference ID 415 Tiffin Ohio — —
Site reference ID 414 Westerville Ohio — —
Site reference ID 419 Bryn Mawr Pennsylvania — —
Site reference ID 449 Jenkintown Pennsylvania — —
Site reference ID 476 Columbia South Carolina — —
Site reference ID 408 Bristol Tennessee — —
Site reference ID 403 Chattanooga Tennessee — —
Site reference ID 429 Nashville Tennessee — —
Site reference ID 452 Austin Texas — —
Site reference ID 461 Beaumont Texas — —
Site reference ID 447 Dallas Texas — —
Site reference ID 460 Dallas Texas — —
Site reference ID 464 Fort Worth Texas — —
Site reference ID 413 Houston Texas — —
Site reference ID 434 Houston Texas — —
Site reference ID 479 Houston Texas — —
Site reference ID 451 San Antonio Texas — —
Site reference ID 402 Schertz Texas — —
Site reference ID 432 Webster Texas — —
Site reference ID 422 Draper Utah — —
Site reference ID 467 Centreville Virginia — —
Site reference ID 407 Norfolk Virginia — —
Site reference ID 412 Richmond Virginia — —
Site reference ID 417 Richmond Virginia — —
Site reference ID 406 Seattle Washington — —

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 15 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02778399, 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 Jul 21, 2022 · Synced Oct 20, 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 NCT02778399 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →