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Recruiting Phase 3 Interventional

A Clinical Study of Sacituzumab Tirumotecan (MK-2870) in Combination With Pembrolizumab (MK-3475) as First-line Maintenance Treatment of Cervical Cancer (MK-2870-036/TroFuse-036/GOG-3123/ENGOT-cx22)

ClinicalTrials.gov ID: NCT07216703

Public ClinicalTrials.gov record NCT07216703. 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 Sep 1, 2026, 4:28 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, Open-label, Multicenter Study to Evaluate the Efficacy and Safety of Sacituzumab Tirumotecan (MK-2870) in Combination With Pembrolizumab With or Without Bevacizumab Compared With Standard of Care as Firstline Maintenance Treatment for Participants With Persistent, Recurrent, or Newly Diagnosed Metastatic Cervical Cancer With PD-L1 CPS Greater Than or Equal to 1 (TroFuse-036/GOG-3123/ENGOT-cx22)

Brief summary

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

Researchers are looking for new ways to treat metastatic cervical cancer. Cervical cancer is cancer in the cervix, the lower part of the uterus (womb). Metastatic means the cancer has spread to other parts of the body. Researchers want to learn about giving the study medicine sacituzumab tirumotecan (also called sac-TMT or MK-2870) along with pembrolizumab and bevacizumab treatments. Sac-TMT is an antibody drug conjugate, which is a type of medicine that attaches to specific targets on cancer cells and delivers treatment to destroy those cells. The goals of this study are to learn: * About the safety of sac-TMT with pembrolizumab and bevacizumab, and if people tolerate them when given together, and * If people who receive sac-TMT and pembrolizumab, with or without bevacizumab, live longer overall or without their cancer getting worse as compared to those who receive standard treatment

Study identification

NCT ID
NCT07216703
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Enrollment
1,023 participants

Conditions and interventions

Interventions

Biological · Drug

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
Jan 18, 2026
Primary completion
Oct 28, 2031
Completion
Oct 28, 2031
Last update posted
Aug 27, 2026

2026 – 2031

United States locations

U.S. sites
23
U.S. states
14
U.S. cities
21
Facility City State ZIP Site status
Florida Cancer Specialists - South ( Site 7001) Fort Myers Florida 33901 Recruiting
Mount Sinai Braman Comprehensive Cancer Center ( Site 5043) Miami Beach Florida 33140 Recruiting
Mount Sinai Comprehensive Cancer Center ( Site 6000) Miami Beach Florida 33140 Recruiting
Florida Cancer Specialists - East ( Site 7000) West Palm Beach Florida 33401 Recruiting
Winship Cancer Institute of Emory University ( Site 5005) Atlanta Georgia 30308 Recruiting
Nancy N. & J.C. Lewis Cancer and Research Pavillion - Research Department ( Site 6005) Savannah Georgia 31405 Recruiting
TRIALS 365 ( Site 6008) Shreveport Louisiana 71103 Recruiting
Maryland Oncology Hematology (MOH) ( Site 8001) Columbia Maryland 21044 Recruiting
Minnesota Oncology Hematology, PA ( Site 8003) Edina Minnesota 55435 Recruiting
Women's Cancer Center of Nevada ( Site 6011) Las Vegas Nevada 89106 Recruiting
Laura and Isaac Perlmutter Cancer Center at NYU Langone ( Site 6009) New York New York 10016 Recruiting
Oklahoma Cancer Specialists and Research Institute, LLC ( Site 6001) Tulsa Oklahoma 74146 Recruiting
Oncology Associates of Oregon, P.C.(Willamette Valley Cancer Institute) (WVCI) ( Site 8007) Eugene Oregon 97401 Recruiting
Asplundh Cancer Pavilion ( Site 5002) Willow Grove Pennsylvania 19090 Recruiting
Women & Infants Hospital ( Site 6003) Providence Rhode Island 02905 Recruiting
University of Tennessee Medical Center ( Site 6012) Knoxville Tennessee 37920 Recruiting
Texas Oncology - DFW ( Site 8005) Fort Worth Texas 76104 Recruiting
Houston Methodist Hospital-Obstetrics and Gynecology ( Site 6010) Houston Texas 77030 Recruiting
Texas Oncology-The Woodlands ( Site 8000) The Woodlands Texas 77380 Recruiting
Texas Oncology - Northeast Texas ( Site 8002) Tyler Texas 75702 Recruiting
University of Virginia Cancer Center ( Site 5044) Charlottesville Virginia 22908 Recruiting
University of Virginia Cancer Center ( Site 6014) Charlottesville Virginia 22908 Recruiting
Inova Schar Cancer Institute ( Site 5045) Fairfax Virginia 22031 Recruiting

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 143 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07216703, 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 27, 2026 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07216703 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →