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Active, not recruiting Phase 3 Interventional

Sacituzumab Tirumotecan (MK-2870) in Post Platinum and Post Immunotherapy Endometrial Cancer (MK-2870-005)

ClinicalTrials.gov ID: NCT06132958

Public ClinicalTrials.gov record NCT06132958. 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 28, 2026, 6:11 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, Active-controlled, Open-label, Multicenter Study to Compare the Efficacy and Safety of MK-2870 Monotherapy Versus Treatment of Physician's Choice in Participants With Endometrial Cancer Who Have Received Prior Platinum-based Chemotherapy and Immunotherapy (MK-2870-005/ENGOT-en23/GOG-3095)

Brief summary

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

Researchers are looking for new ways to treat people with endometrial cancer (EC) who have previously received treatment with platinum based therapy (a type of chemotherapy) and immunotherapy. Immunotherapy is a treatment that helps the immune system fight cancer. This clinical study will compare sacituzumab tirumotecan to chemotherapy. The goal of the study is to learn if people who receive sacituzumab tirumotecan live longer overall and without the cancer getting worse compared to people who receive chemotherapy.

Study identification

NCT ID
NCT06132958
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Enrollment
710 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
Dec 6, 2023 (Actual)
Primary completion
Jan 10, 2028 (Estimated)
Completion
Jan 10, 2028 (Estimated)
Last update posted
Aug 28, 2026

2023 – 2028

United States locations

U.S. sites
43
U.S. states
25
U.S. cities
42
Facility City State ZIP Site status
USA Mitchell Cancer Institute ( Site 4142) Mobile Alabama 36604 —
Alaska Womens Cancer Care ( Site 4122) Anchorage Alaska 99508 —
HonorHealth (HH) ( Site 8000) Phoenix Arizona 85016 —
Arizona Oncology Associates - HOPE ( Site 8002) Tucson Arizona 85711 —
UCLA Hematology/Oncology - Westwood (Building 100)-Department of OBGYN, Division of Gynecologic Onc ( Site 4131) Los Angeles California 90095 —
California Pacific Medical Center - Van Ness Campus ( Site 4129) San Francisco California 94109 —
Yale-New Haven Hospital-Smilow Cancer Hospital at Yale-New Haven ( Site 4114) New Haven Connecticut 06511 —
MedStar Washington Hospital Center ( Site 4108) Washington D.C. District of Columbia 20010 —
Mount Sinai Cancer Center ( Site 4117) Miami Beach Florida 33140 —
AdventHealth Orlando-AdventHealth Medical Group Gynecological Oncology ( Site 4113) Orlando Florida 32804 —
Florida Cancer Specialists - East ( Site 7000) West Palm Beach Florida 33401 —
Northside Hospital ( Site 4112) Atlanta Georgia 30342 —
Augusta University ( Site 4116) Augusta Georgia 30912 —
Centricity Research Columbus Cancer Center ( Site 4154) Columbus Georgia 31904 —
NorthShore University HealthSystem - Evanston Hospital ( Site 4110) Evanston Illinois 60201 —
Parkview Research Center at Parkview Regional Medical Center ( Site 4132) Fort Wayne Indiana 46845 —
Saint Elizabeth Medical Center Edgewood-Cancer Care Center ( Site 4150) Edgewood Kentucky 41017 —
University Medical Center New Orleans ( Site 4133) New Orleans Louisiana 70112 —
TRIALS 365 ( Site 4105) Shreveport Louisiana 71103 —
University of Massachusetts Memorial Medical Center ( Site 4103) Worcester Massachusetts 01605 —
Washington University School of Medicine-Obstetrics & Gynecology ( Site 4146) St Louis Missouri 63110 —
The Center of Hope ( Site 4109) Reno Nevada 89511 —
John Theurer Cancer Center at Hackensack University Medical Center ( Site 4118) Hackensack New Jersey 07601 —
Atlantic Health System Morristown Medical Center ( Site 4135) Morristown New Jersey 07960 —
Holy Name Medical Center ( Site 4115) Teaneck New Jersey 07666 —
New York - Presbyterian Brooklyn Methodist Hospital ( Site 4134) Brooklyn New York 11215 —
Perlmutter Cancer Center at NYU Langone Hospital - Long Island ( Site 4156) Mineola New York 11501 —
Laura and Isaac Perlmutter Cancer Center ( Site 4106) New York New York 10016 —
Icahn School of Medicine at Mount Sinai-Department of Obstetrics, Gynecology, and Reproductive Scie ( Site 4128) New York New York 10029 —
Good Samaritan Hospital Medical Center ( Site 4139) West Islip New York 11795 —
Duke Cancer Institute ( Site 4120) Durham North Carolina 27710 —
Sanford Health Roger Maris Cancer Center ( Site 4158) Fargo North Dakota 58102 —
University of Cincinnati Medical Center ( Site 4136) Cincinnati Ohio 45219 —
The James Cancer Hospital and Solove Research Institute at The Ohio State University Comprehensive C (Site 4125) Columbus Ohio 43210 —
Sidney Kimmel Cancer Center - Jefferson Health ( Site 4157) Philadelphia Pennsylvania 19107 —
AHN West Penn Hospital-Gynecologic Oncology ( Site 4111) Pittsburgh Pennsylvania 15244 —
Asplundh Cancer Pavilion ( Site 4107) Willow Grove Pennsylvania 19090 —
Women & Infants Hospital ( Site 4138) Providence Rhode Island 02905 —
Sanford Cancer Center-Gynecologic Oncology ( Site 4121) Sioux Falls South Dakota 57104 —
The West Clinic, PLLC dba West Cancer Center ( Site 4102) Germantown Tennessee 38138 —
Houston Methodist Hospital-Obstetrics and Gynecology ( Site 4130) Houston Texas 77030 —
Texas Oncology - San Antonio ( Site 8005) San Antonio Texas 78240 —
Texas Oncology - Gulf Coast ( Site 8006) The Woodlands Texas 77380 —

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 199 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06132958, 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 Aug 28, 2026 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06132958 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →