Independent directory Public ClinicalTrials.gov records United States
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 Oct 25, 2026, 11:37 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 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)

Brief summary

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

This is a 2 part study. Part 1 is to evaluate the efficacy and safety of dostarlimab plus carboplatin-paclitaxel followed by dostarlimab versus placebo plus carboplatin-paclitaxel followed by placebo; and Part 2 is to evaluate the efficacy and safety of dostarlimab plus carboplatin-paclitaxel followed by dostarlimab plus niraparib versus placebo plus carboplatin-paclitaxel followed by placebo in participants with recurrent or primary advanced (Stage III or IV) endometrial cancer.

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

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 18, 2019 (Actual)
Primary completion
Nov 26, 2026 (Estimated)
Completion
Nov 26, 2026 (Estimated)
Last update posted
Sep 3, 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 3, 2025 · Synced Oct 25, 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 NCT03981796 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →