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Recruiting Phase 3 Interventional

A Clinical Trial of Sac-TMT in People With Non-HRD Positive Advanced Ovarian Cancer (MK-2870-021)

ClinicalTrials.gov ID: NCT07318558

Public ClinicalTrials.gov record NCT07318558. 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, 10:07 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 of Sacituzumab Tirumotecan (Sac-TMT, MK-2870) Maintenance Treatment With or Without Bevacizumab Versus Standard of Care in Participants With Newly Diagnosed Advanced Non-HRD Positive Ovarian Cancer Following First-line Platinum-based Chemotherapy (TroFuse-021/ENGOTov85/GOG-3102)

Brief summary

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

Researchers are looking for new ways to treat ovarian cancer (OC). Current treatment for OC may start with surgery to remove as much of the cancer as possible. After surgery, people may receive chemotherapy. After chemotherapy, standard care options may include: * Maintenance treatment, which is used after another therapy to keep the cancer from growing, spreading, or coming back. Bevacizumab is a targeted therapy used as standard maintenance treatment. Targeted therapy works to control how specific types of cancer cells grow and spread. * Observation, which is watching to see if cancer grows or worsens The study medicine, sacituzumab tirumotecan (also called sac-TMT), is a targeted therapy. The goal of this study is to learn if people who receive sac-TMT maintenance treatment with or without bevacizumab live longer without the cancer getting worse than people who receive standard care.

Study identification

NCT ID
NCT07318558
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Enrollment
900 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
Feb 15, 2026
Primary completion
Feb 24, 2033
Completion
Feb 24, 2033
Last update posted
Aug 27, 2026

2026 – 2033

United States locations

U.S. sites
25
U.S. states
19
U.S. cities
24
Facility City State ZIP Site status
University of Alabama - Birmingham ( Site 0058) Birmingham Alabama 35233 Recruiting
John Muir Health Cancer Center ( Site 0069) Walnut Creek California 94598 Recruiting
Mount Sinai Cancer Center ( Site 0029) Miami Beach Florida 33140 Recruiting
Orlando Health Winnie Palmer Hospital for Women and Babies ( Site 0085) Orlando Florida 32806 Recruiting
Winship Cancer Institute of Emory University ( Site 0037) Atlanta Georgia 30308 Recruiting
Illinois Cancer Specialists (ICS) ( Site 8009) Arlington Heights Illinois 60005 Recruiting
Parkview Research Center at Parkview Regional Medical Center ( Site 0055) Fort Wayne Indiana 46845 Recruiting
Franciscan Health Indianapolis ( Site 0081) Indianapolis Indiana 46237 Recruiting
Women's Cancer Care ( Site 0018) Covington Louisiana 70433 Recruiting
Maine Medical Center Research Institute-MaineHealth/Maine Medical Partners - GynOnc ( Site 0060) Scarborough Maine 04074 Recruiting
Maryland Oncology Hematology, P.A. ( Site 8002) Columbia Maryland 21044 Recruiting
Nebraska Methodist Hospital ( Site 0004) Omaha Nebraska 68114 Recruiting
University Of Nebraska Medical Center ( Site 0035) Omaha Nebraska 68198 Recruiting
The Center of Hope ( Site 0025) Reno Nevada 89511 Recruiting
Womens Cancer Care Associates, LLC ( Site 0023) Albany New York 12208-1743 Recruiting
Duke Cancer Center ( Site 0012) Durham North Carolina 27710 Recruiting
University of Cincinnati Medical Center ( Site 0042) Cincinnati Ohio 45219 Recruiting
Oklahoma Cancer Specialists and Research Institute, LLC ( Site 0007) Tulsa Oklahoma 74146 Recruiting
Hospital of the University of Pennsylvania ( Site 0071) Philadelphia Pennsylvania 19104 Recruiting
Women & Infants Hospital ( Site 0001) Providence Rhode Island 02905 Recruiting
West Cancer Center and Research Institute ( Site 0013) Germantown Tennessee 38138 Recruiting
University of Tennessee Medical Center ( Site 0087) Knoxville Tennessee 37920 Recruiting
Henry-Joyce Cancer Clinic ( Site 0011) Nashville Tennessee 37232 Recruiting
Virginia Cancer Specialists (VCS) ( Site 8012) Fairfax Virginia 22031 Recruiting
Virginia Oncology Associates (VOA) ( Site 8013) Norfolk Virginia 23502 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 134 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07318558, 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 NCT07318558 live on ClinicalTrials.gov.

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