ClinicalTrials.gov record
Active, not recruiting Phase 3 Interventional

A Study to Evaluate Dostarlimab Plus Carboplatin-paclitaxel Versus Placebo Plus Carboplatin-paclitaxel in Participants With Recurrent or Primary Advanced Endometrial Cancer

ClinicalTrials.gov ID: NCT03981796

Public ClinicalTrials.gov record NCT03981796. 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 May 6, 2026, 2:07 AM 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 Phase 3, Randomized, Double-blind, Multicenter Study of Dostarlimab (TSR-042) Plus Carboplatin-paclitaxel Versus Placebo Plus Carboplatin-paclitaxel in Patients With Recurrent or Primary Advanced Endometrial Cancer (RUBY)

Study identification

NCT ID
NCT03981796
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Tesaro, Inc.
Industry
Enrollment
785 participants

Conditions and interventions

Conditions

Interventions

  • Carboplatin Drug
  • Dostarlimab Biological
  • Niraparib Drug
  • Paclitaxel Drug
  • Placebo matching Niraparib Drug
  • Placebo matching dostarlimab Drug

Drug · Biological

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
Jul 17, 2019
Primary completion
Nov 25, 2026
Completion
Nov 25, 2026
Last update posted
Sep 2, 2025

2019 – 2026

United States locations

U.S. sites
59
U.S. states
24
U.S. cities
52
Facility City State ZIP Site status
GSK Investigational Site Phoenix Arizona 85016
GSK Investigational Site Scottsdale Arizona 85016
GSK Investigational Site Tucson Arizona 85704
GSK Investigational Site Tucson Arizona 85710
GSK Investigational Site Newport Beach California 92663
GSK Investigational Site Palo Alto California 94304
GSK Investigational Site Deerfield Beach Florida 33442
GSK Investigational Site Jacksonville Florida 32207
GSK Investigational Site Miami Florida 33136
GSK Investigational Site Miami Florida 33176
GSK Investigational Site Orlando Florida 32804
GSK Investigational Site Atlanta Georgia 30342
GSK Investigational Site Augusta Georgia 30912
GSK Investigational Site Savannah Georgia 31405
GSK Investigational Site Hinsdale Illinois 60521
GSK Investigational Site Zion Illinois 60099
GSK Investigational Site Fort Wayne Indiana 46845
GSK Investigational Site Indianapolis Indiana 46202
GSK Investigational Site Indianapolis Indiana 46260
GSK Investigational Site Iowa City Iowa 52242
GSK Investigational Site Lexington Kentucky 40536
GSK Investigational Site Covington Louisiana 70433
GSK Investigational Site New Orleans Louisiana 70121
GSK Investigational Site Shreveport Louisiana 71103
GSK Investigational Site Boston Massachusetts 02114
GSK Investigational Site Springfield Massachusetts 01199
GSK Investigational Site Detroit Michigan 48201
GSK Investigational Site St Louis Missouri 63108
GSK Investigational Site Lebanon New Hampshire 03756
GSK Investigational Site Albuquerque New Mexico 87131
GSK Investigational Site Rio Rancho New Mexico 87124
GSK Investigational Site Albany New York 12208
GSK Investigational Site Mineola New York 10016
GSK Investigational Site New York New York 10016
GSK Investigational Site The Bronx New York 10461
GSK Investigational Site Charlotte North Carolina 28204
GSK Investigational Site Durham North Carolina 27710
GSK Investigational Site Kernersville North Carolina 27284
GSK Investigational Site Mount Airy North Carolina 27030
GSK Investigational Site Winston-Salem North Carolina 27103
GSK Investigational Site Cincinnati Ohio 45219
GSK Investigational Site Cincinnati Ohio 45220
GSK Investigational Site Cleveland Ohio 44106
GSK Investigational Site Columbus Ohio 43210
GSK Investigational Site Hilliard Ohio 43026
GSK Investigational Site Hilliard Ohio 43210
GSK Investigational Site Tulsa Oklahoma 74146
GSK Investigational Site Philadelphia Pennsylvania 19111
GSK Investigational Site Pittsburgh Pennsylvania 15224
GSK Investigational Site Willow Grove Pennsylvania 19090
GSK Investigational Site Providence Rhode Island 02905
GSK Investigational Site Knoxville Tennessee 37920
GSK Investigational Site Austin Texas 78731
GSK Investigational Site Austin Texas 78758
GSK Investigational Site Dallas Texas 75246
GSK Investigational Site Dallas Texas 76104
GSK Investigational Site Charlottesville Virginia 22903
GSK Investigational Site Roanoke Virginia 24016
GSK Investigational Site Seattle Washington 98109

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 110 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03981796, 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 Sep 2, 2025 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03981796 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →