A study of sacituzumab tirumotecan and bevacizumab in patients with newly diagnosed advanced ovarian cancer following first-line platinum-based chemotherapy

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What is this study about?

This study focuses on individuals with newly diagnosed advanced Ovarian Cancer that is HRD-negative, which means the cancer cells have a specific type of genetic profile related to how they repair their DNA. The purpose of this study is to compare a maintenance treatment using MK-2870, also known as sacituzumab tirumotecan, either alone or combined with bevacizumab, against the current standard medical care. Maintenance treatment refers to therapy given to keep the cancer from growing again after the initial main treatment has finished.

Participants in the study will receive medications through an intravenous infusion, which is a method of delivering medicine directly into a vein. The study involves comparing different combinations of drugs to see how they affect progression-free survival, a term used to describe the length of time during and after treatment that a person lives with the disease without it getting worse. Other factors being observed include overall survival and the quality of life, which tracks how well a person can perform daily activities and their general well-being during the study.

Who Can Join the Study?

  • Must be a female patient.
  • Must be between the ages of 12 and 17 years old.
  • Must have a confirmed diagnosis of epithelial ovarian cancer, primary peritoneal cancer, or fallopian tube cancer that is at Stage III or Stage IV, which means the cancer has grown or spread significantly.
  • Must have finished a debulking surgery, which is a procedure to remove as much of the tumor as possible from the body.
  • Must have completed their first round of platinum-based chemotherapy, which is a type of medicine used to kill cancer cells.
  • The cancer must have shown a stable disease (meaning it did not grow), a partial response (meaning the tumor shrank), or a complete response (meaning no cancer was found) after the first treatment.
  • Must be able to provide a tumor tissue sample that has not been treated with radiation (high-energy beams used to kill cancer cells).
  • If the patient has HIV (a virus that affects the immune system), it must be well-controlled using antiretroviral therapy (medicines used to manage the virus).
  • If the patient has Hepatitis B (a virus that affects the liver), the viral load (the amount of virus in the blood) must be undetectable, and they must be taking antiviral therapy (medicine to fight the virus).
  • If the patient has a history of Hepatitis C (another virus that affects the liver), the viral load must be undetectable.

Who Cannot Join the Study?

  • Having types of cancer other than the specific ovarian cancer being studied, such as nonepithelial cancers, borderline tumors (growths that are not fully cancerous), mucinous tumors (tumors that produce mucus), malignant Brenner’s tumors, or undifferentiated carcinoma (cancer cells that do not look like normal cells).
  • Having an active infection (a current illness caused by germs) that requires systemic therapy (medicine that travels through the entire body).
  • Having current infections of the Hepatitis B virus (HBV) or Hepatitis C virus (HCV), which are viruses that affect the liver.
  • Having an HIV infection or a history of Kaposi’s sarcoma or multicentric Castleman’s disease (types of rare cancers or disorders affecting the immune system).
  • Not having fully recovered from a major surgery or having ongoing problems caused by a recent surgery.
  • Having active central nervous system (CNS) metastases (cancer that has spread to the brain or spine) or carcinomatous meningitis (cancer that has spread to the protective layers covering the brain and spinal cord).
  • Having a history of severe eye disease.
  • Having active inflammatory bowel disease (a condition causing swelling in the digestive tract) that requires immunosuppressive medication (drugs that lower the body’s immune response) or having had this disease in the past.
  • Having uncontrolled cardiovascular disease (serious heart problems) or cerebrovascular disease (problems with blood flow to the brain, such as a stroke).
  • Having a history of, or currently having, pneumonitis (inflammation of the lung tissue) or interstitial lung disease (ILD) (a group of disorders that cause scarring of lung tissue) that required the use of steroids (strong anti-inflammatory medicines).
  • Having received prior systemic anticancer therapy (previous treatments like chemotherapy that travel through the bloodstream to fight cancer).
  • Having received a live or live-attenuated vaccine (a vaccine containing a weakened form of a germ) within 30 days before being assigned to the study groups.
  • Having another type of malignancy (cancer) that is growing or required active treatment within the last 3 years.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Medical University Of Vienna Vienna Austria
University Hospital Jena KöR Jena Germany
Centre Hospitalier Regional Et Universitaire De Brest Brest France
Medizinische Universitaet Innsbruck Innsbruck Austria
Institut Gustave Roussy Villejuif France
Oncopole Claudius Regaud Toulouse France
Technische Universitaet Dresden Dresden Germany
Katholieke Universiteit te Leuven Leuven Belgium
Fondazione Policlinico Universitario Agostino Gemelli IRCCS Rome Italy
Oslo Universitetssykehus HF Oslo Norway
Hospital Universitario De Navarra Pamplona Spain
Centre Jean Perrin Clermont Ferrand France
Comite Entreprise Paul Papin Angers France
Kuopio University Hospital Kuopio Finland

Other Sites

Site Name City Country Status
University Hospital Ostrava Ostrava Czechia
Fakultni Nemocnice Hradec Kralove Novy Hradec Kralove Czechia
Karolinska University Hospital Solna Sweden
Semmelweis University Budapest Hungary
Turku University Hospital Turku Finland
Istituto Europeo Di Oncologia S.r.l. Milan Italy
Azienda Ospedaliero Universitaria Di Modena Modena Italy
Az Maria Middelares Gent Gent Belgium
Uniwersytecki Szpital Kliniczny W Poznaniu Poznan Poland
Fakultni Nemocnice Bulovka Prague Czechia
Mazowiecki Szpital Wojewodzki Im. Sw. Jana Pawła II W Siedlcach Sp. z o.o. Siedlce Poland
Ixeubmzg Jgtzs Bjmkuy Anderlecht Belgium
Urazrsxxbo Oy Dfcfxtks Debrecen Hungary
Izimrwpw Pbcougnvcwlwwxt Ceyows Cuyshp Marseille France
Hdgrhbfk Vkwm dxfrudmq Barcelona Spain
Hjfpxpbt Ubokmbijfvyew dn A Cgwbhe A Coruna Galicia Spain
Ftwpkqhm nnoronsbe Mdthk a Hwtzvzv Prague Czechia
Oeqrkm Urxrroqaxo Hcekgbmi Odense Denmark
Hnpclo Hoiqjnxx Herlev Denmark
Abllkjxff Hdlyzghd Athens Greece
Hbifdewn Czydqu Du Bijszskan Barcelona Spain
Cvgeqwe Uhrfwrrmuiwsakxffnux Bqqgvt Kgn Berlin Germany
Foopjvid Ntevpipcc Bbqf Brno Czechia
Cedwzw Hrqeicwqqnr Rbawkmqo Uglozodbxeqny Dt Thduu Tours France
Fyjzvhmn Nvrolufav Kbnnwyugj Vrikwusok Prague Czechia
Hshzllem Chkclds Sks Czfdux Madrid Spain
Aitpymq Uglzxvpghb Hnduppmm Aalborg Denmark
Jvhokajw Ktjfsp Uukfdmyncd Linz Austria
Kokajnul Kmekja Gmhe Kassel Germany
Rstbog Mpjfplyarxr Aarhus Denmark
Vnjmamctm Fggooioh Ncxiarwss V Pgbsn Prague Czechia
Umdororavhxb Lasyztg Leipzig Germany
Si Vdyhldwucmwscch Uzkkynsmdd Huwodolp Dublin Ireland
Cafkhc Lasv Bqpohj Lyon France
Uffdyjwhowhkwophbjxxt Ahbwlw Aze Aachen Germany
Hcegq Seazwpmjj Hh Stavanger Norway
Iunkbcpy Cewyjn Defevxxjxmnfnmwjg L'hospitalet De Llobregat Spain
Uulkqtesuf Dttgq Sansw Dl Bnmtnaj Brescia Italy
Fbsidpdbs Poti Lu Itmxuwdakbfry Bsqhspvwe Das Hcceleqd Uxclzzbdgqazy Ll Pnz Madrid Spain
Fbyqxyjda Ixknawnro Vbomkgsyhs Dp Oxtqthmaj Valencia Spain
Ouvv Uxwzkkhuna Hguhjens Oulu Finland
Fojlcxvamo Izwikdjmzm Iojpudex Nyyfizrdrtg Bbhvw Milan Italy
Hqzafgbr Ulmjldlbivuwnd Sxnfdqjwlu &jcyuge Hopncdl dx Hemjqcpknpr STRASBOURG, Alsace France
Itopgdue Oztgphebbx Vlsmwk Padua Italy
Itzumgvy Rveqwtmj Dm Cvgjfa Dn Mqwugbtpzjz Montpellier France
Ojkytbok Oznchilkef Iljlavu Budapest Hungary
Bflwpcfacrn Vtbnthaqt Omsepevofmup Kecskemet Hungary
Kvkhycus Luvcl Gqep Detmold Germany
Sqyfcmosy sqcwhfd Kjatgwzfbiwc Kristiansand Norway
Cpctjd Ojhnv Lwryyer Lille France
Uqxotenwnuknd Sknxsho Kvshipmnq Nl 2 Plh W Srgijqbcrf Szczecin Poland
Cjccec Hbpvfvvkfof Ee Uxyyatfjwlufy Dy Lzlrbly Limoges France
Ahdcauhiwo Mukjshj Huttmdty Lecco Italy
Gxxqfejkvullajnnh Vdjxqqxce Pifg Atcghl Epcrmies Osivmg Kgrifu Gyor Hungary
Nzuuonhp Iteiwuvd Orlwnduuf Ius Mdaaz Shibiwecdiizzgboeaqouewaicto Ijzrjxhl Bqqyosfg Cracow Poland
Hesmhrb Ptoax Dwq Cnmtx Dmqhboqttrimw Plerin France
Srn Lphlvhgcmhvh Hptxjolt Sqfr Thessaloniki Greece
Eihmdsrkcp Cqbdvr Abql Txeva Shzq Athens Greece
Pxuqnhedki hhnxnpvlevaquau Tampere Finland
Rhpfah Oqdycakbbwpcka Linkoping Sweden
Cwno Uegajlcxuk Hsidelfy Cork Ireland
Gmazh Hbvejqg Da Cpabnrylx Charleroi Belgium
Wzhtyoysbzzgx Ctnlbjb Ojsrtjywb Ikq Mkrmp Szizuamofltxrfrvhy Poznan Poland
Altsmzr Ozwhifrvkvm Ovbexk Mutpqhghxq Dr Tiagar Turin Italy
Brkjlywryjqw Cgjhvzh Ograqxcaa Iyj Moqrn Sfvcazrcmfikzfzvrt W Biqwpyblciu Bialystok Poland

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Austria Austria
Recruiting
15.04.2026
Belgium Belgium
Recruiting
15.04.2026
Czechia Czechia
Recruiting
15.04.2026
Denmark Denmark
Recruiting
15.04.2026
Finland Finland
Recruiting
15.04.2026
France France
Recruiting
15.04.2026
Germany Germany
Not yet recruiting
15.04.2026
Greece Greece
Recruiting
15.04.2026
Hungary Hungary
Recruiting
15.04.2026
Ireland Ireland
Recruiting
15.04.2026
Italy Italy
Recruiting
15.04.2026
Norway Norway
Recruiting
15.04.2026
Poland Poland
Recruiting
15.04.2026
Spain Spain
Recruiting
15.04.2026
Sweden Sweden
Recruiting
15.04.2026

Trial locations

Sacituzumab tirumotecan is a medication administered through an intravenous infusion. It is being studied as a maintenance treatment to help manage advanced ovarian cancer after a patient has completed their first round of platinum-based chemotherapy.

Bevacizumab is a medication given through an intravenous infusion. In this study, it is used either alongside sacituzumab tirumotecan or as part of the standard care to help treat advanced ovarian cancer.

Investigated Diseases:

Ovarian cancer – This disease occurs when harmful cells grow uncontrollably in the ovaries. These cells can form masses or tumors that disrupt normal organ function. The condition often begins in the surface cells of the ovary and can spread to nearby tissues or other parts of the body. As the disease progresses, the abnormal cells may move through the pelvic area or the abdominal cavity. This spreading process can lead to various changes in how the reproductive system and surrounding organs operate.

Trial ID:
2023-508047-40-00
Protocol code:
MK-2870-021
Trial Phase:
Therapeutic confirmatory (Phase III)

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