Comparison of Niraparib alone versus Niraparib with Bevacizumab in patients with newly diagnosed advanced ovarian cancer after chemotherapy with carboplatin and paclitaxel

3 1 1 1

What is this study about?

This clinical trial focuses on patients with newly diagnosed advanced ovarian cancer, peritoneal cancer, or fallopian tube cancer. The study compares two treatment approaches using several medications. All patients will initially receive chemotherapy with carboplatin and paclitaxel, which are standard cancer drugs given through an intravenous infusion.

After the initial chemotherapy, patients will be divided into two groups. One group will receive a medication called niraparib alone, while the other group will receive niraparib combined with bevacizumab. Niraparib is taken as a capsule by mouth, while bevacizumab is given through an intravenous infusion. The purpose of this study is to determine if adding bevacizumab to niraparib treatment leads to better results than using niraparib alone.

The study will monitor how long patients remain without their cancer getting worse. Patients will receive regular medical examinations and tests throughout the study period. The treatment may continue for up to 36 months, depending on how well patients respond to the therapy and whether they experience any side effects.

1 Initial chemotherapy phase

You will receive a combination of paclitaxel and carboplatin through intravenous infusion

During this phase, some patients will also receive bevacizumab through intravenous infusion

The treatment will begin within 8 weeks after surgery

2 Maintenance treatment phase

After completing chemotherapy, you will receive niraparib capsules taken by mouth

Some patients will continue receiving bevacizumab through intravenous infusion along with niraparib

The specific treatment group will be determined randomly

3 Regular monitoring

Your health will be monitored through regular medical examinations

Blood tests will check your liver and kidney function

Blood pressure measurements will be taken regularly

Imaging tests will be performed to assess the cancer’s response to treatment

4 Quality of life assessment

You will be asked to complete questionnaires about your symptoms and quality of life

These assessments help monitor how the treatment affects your daily life

5 Long-term follow-up

Your progress will be monitored until 2031

Regular check-ups will continue to assess your response to treatment

Any side effects or health changes will be documented and managed

Who Can Join the Study?

  • Must be female and at least 18 years old
  • Must have been diagnosed with advanced ovarian, peritoneal, or fallopian tube cancer that has been confirmed through tissue examination
  • Must have either already had initial surgery or be planning to have chemotherapy followed by surgery
  • Must be able to start treatment within 8 weeks after surgery
  • Must have good physical function (able to carry out all normal activities with minimal limitations)
  • Must have a life expectancy of more than 3 months
  • Must have adequate blood test results showing:
    – Normal liver and kidney function
    – Good blood cell counts
    – Normal blood clotting ability
  • Must have normal blood pressure or well-controlled blood pressure (140/90 or lower)
  • Must provide a tissue sample for BRCA genetic testing
  • For women who can become pregnant:
    – Must have a negative pregnancy test
    – Must use highly effective birth control or remain abstinent during treatment and for 6 months after
  • Must be willing and able to:
    – Attend scheduled appointments
    – Follow treatment plans
    – Complete required laboratory tests
    – Fill out questionnaires
  • Must sign an informed consent form showing understanding of and willingness to participate in the study

Who Cannot Join the Study?

  • Prior chemotherapy, radiotherapy, hormonal therapy, immunotherapy, or any other systemic anti-cancer treatment for ovarian cancer
  • History of other cancers within the last 5 years (except successfully treated non-melanoma skin cancer or cervical carcinoma in situ)
  • Known brain metastases (cancer that has spread to the brain)
  • Significant cardiovascular disease, including:
    • Uncontrolled high blood pressure
    • Heart attack within past 6 months
    • Unstable angina (chest pain)
    • Severe heart rhythm problems
  • Major surgery within 4 weeks before starting treatment
  • Active bleeding or high risk of bleeding
  • Serious infections requiring antibiotics
  • Pregnancy or breastfeeding
  • Known allergies to any of the study medications
  • Inability to swallow oral medications
  • Serious medical conditions that could interfere with study participation
  • Thromboembolism (blood clots) within the past 6 months
  • Inadequate organ function, including:
    • Poor kidney function
    • Poor liver function
    • Low blood cell counts
  • Psychiatric disorders or conditions that would interfere with following study requirements

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Other Sites

Site Name City Country Status
Klinikum Frankfurt Hoechst GmbH Frankfurt Germany
Klinikum Dortmund gGmbH Dortmund Germany
HELIOS Klinikum Krefeld GmbH Krefeld Germany
Staedtisches Klinikum Karlsruhe gGmbH Karlsruhe Germany
St. Vincenz-Krankenhaus GmbH Paderborn Germany
Universitair Ziekenhuis Gent Gent Belgium
Klinikum Mutterhaus der Borromaeerinnen gGmbH Trier Germany
Leopoldina-Krankenhaus der Stadt Schweinfurt GmbH Schweinfurt Germany
SRH Wald-Klinikum Gera GmbH Gera Germany
Universitaetsklinikum Brandenburg an der Havel GmbH Brandenburg An Der Havel Germany
Centre Hospitalier Universitaire Dinant Godinne Sainte-Elisabeth-UCL-Namur Namur Belgium
Johannes Wesling Klinikum Minden Minden Germany
Gesundheit Nord gGmbH Klinikverbund Bremen Bremen Germany
Klinikum St Marien Amberg Amberg Germany
Klinikum Esslingen GmbH Esslingen Am Neckar Germany
RKH Klinken Ludwigsburg-Bietigheim gGmbH Ludwigsburg Germany
St. Josefs-Hospital Wiesbaden GmbH Wiesbaden Germany
Hochtaunus-Kliniken gGmbH Bad Homburg Germany
HELIOS Klinikum Berlin-Buch GmbH Berlin Germany
Klinikverbund Allgaeu gGmbH Kempten (Allgau) Germany
Barmherzige Brueder gemeinnuetzige Krankenhaus GmbH Regensburg Germany
Mammazentrum Hamburg MVZ GbR Hamburg Germany
Klinikum Magdeburg gGmbH Magdeburg Germany
Klinikum Hanau GmbH Hanau Germany
Ortenau Klinikum Offenburg Germany
Staedtisches Krankenhaus Kiel GmbH Kiel Germany
Philipps-Universitaet Marburg Marburg Germany
Universitaetsklinikum Schleswig-Holstein AöR Kiel Germany
Universitaetsklinikum Tuebingen AöR Tuebingen Germany
Klinikum Der Landeshauptstadt Stuttgart gKAöR Stuttgart Germany
Universitaetsklinikum Magdeburg AöR Magdeburg Germany
Charite Universitaetsmedizin Berlin KöR Berlin Germany
SLK-Kliniken Heilbronn GmbH Heilbronn Germany
Klinikum Worms gGmbH Worms Germany
Klinikum Suedstadt Rostock Rostock Germany
St. Elisabeth Krankenhaus GmbH Cologne Germany
Klinikum Chemnitz gGmbH Chemnitz Germany
Universitaetsklinikum Mannheim GmbH Mannheim Germany
Kaiserswerther Diakonie Duesseldorf Germany
Klinikum Kassel GmbH Kassel Germany
Justus-Liebig-Universitaet Giessen Giessen Germany
Medical Center – University Of Freiburg Freiburg Im Breisgau Germany
Kliniken Suedostbayern AG Traunstein Germany
Rotkreuzklinikum Muenchen gGmbH Munich Germany
Klinikum Konstanz GmbH Konstanz Germany
Institut fuer Klinische Transfusionsmedizin und Immungenetik Ulm gGmbH Ulm Germany
Studienzentrum Onkologie Ravensburg GmbH Ravensburg Germany
Romed Klinikum Rosenheim Rosenheim Germany
Istituto Oncologico Veneto Padua Italy
Alessandro Manzoni Hospital Lecco Italy
Azienda Ospedaliera Ordine Mauriziano Di Torino Turin Italy
Fakultni Nemocnice Brno Brno Czechia
Vseobecna Fakultni Nemocnice V Praze Prague Czechia
Fakultni Nemocnice Bulovka Prague Czechia
Universitaetsklinikum Leipzig AöR Leipzig Germany
Thueringen-Kliniken Georgius Agricola GmbH Saalfeld Germany
AUSL Piacenza – Ospedale “Guglielmo Da Saliceto” Piacenza Italy
Azienda Usl Toscana nord ovest – Ospedale San Luca Lucca Italy
Gynäkologie Kompetenzzentrum Stralsund Gynäkologische Praxis Dr. med. Carsten Hielscher Stralsund Germany
MVZ Nordhausen Nordhausen Germany
Kppjirxvqwekr Rbulpnjyaf Guig Reutlingen Germany
Usoozosfug Mkpeezu Cwpwlx Hliogctvtizsftqnv Hamburg Germany
Uerpqioicrcpewswoijpv Eapne Avk Essen Germany
Uvwdhudtohhrsdjdnyaca Aaqzlzwa Augsburg Germany
Kyqsqevqjwwedbyqxrynner Ske Vffwgfz mds Limburg Germany
Kdgneoqg Ggokhlmqoc gpzxf Guetersloh Germany
Oqusyaamulxu Shlbejnaytgmnkktl Bielefeld Germany
Uadiczczmx Hsjizzxz Cosabqi Cologne Germany
Uwhccdwudikkusphvfpju Moufzpxw Alc Munster Germany
Kbfvdyqq dcl Uxozvbnuirty Mqgkviar Alu Munich Germany
Mgqberkmsvtqxvqrdibecinhsc Hkzmenfcqzbwmdnp Halle (Saale) Germany
Keekfpow Evrgrscnypibfotujyjbrxoe Hblehsmbitaogctez Essen Germany
Oekmnimj Iglovuk dp Rkvsaw Rimini Italy
Axbtqyi Umu Ieftl Du Riijyb Egcygn Reggio Emilia Italy
Vhddn Ceaniusxuiv Khyporuh Kxdvvpkzb Karlsruhe Germany
Uepekjaiwtswtjxedpogl Dcmujohslrv Aeo Duesseldorf Germany
Gfvgqh Urqhqpcfeu Fpumjpfje Frankfurt Germany

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

Trial status

Country Status Recruitment Start
Belgium Belgium
Not yet recruiting
01.09.2022
Czechia Czechia
Not yet recruiting
01.09.2022
Germany Germany
Recruiting
01.09.2022
Italy Italy
Not yet recruiting
01.09.2022

Trial locations

Niraparib is a medication that belongs to a class of drugs called PARP inhibitors. It works by blocking an enzyme that cancer cells need to repair their DNA, which can help stop cancer cells from growing. It is taken as an oral medication and is used in the treatment of ovarian cancer.

Bevacizumab is a targeted therapy that works by blocking the formation of new blood vessels that feed tumors. It belongs to a class of drugs called angiogenesis inhibitors. This medication is given through an intravenous (IV) infusion and helps prevent tumors from growing by cutting off their blood supply.

Carboplatin is a chemotherapy medication that belongs to a group of drugs called platinum compounds. It works by interfering with cancer cell DNA, preventing cancer cells from dividing and growing. It is given through an intravenous (IV) infusion.

Paclitaxel is a chemotherapy medication that belongs to a class of drugs called taxanes. It works by stopping cancer cells from dividing and growing. This medication is given through an intravenous (IV) infusion and is commonly used in combination with other cancer treatments.

Ovarian Cancer – A disease that begins in the ovaries when cells start growing abnormally. It typically develops in the cells that make up the outer surface of the ovary. The cancer can spread within the pelvis and abdomen.

Peritoneal Cancer – A rare cancer that develops in the peritoneum, the thin layer of tissue that lines the abdomen and covers most of the abdominal organs. It behaves similarly to ovarian cancer and produces similar symptoms.

Fallopian Tube Cancer – A disease that begins in the fallopian tubes, which connect the ovaries to the uterus. The cancer starts in the cells of the fallopian tube lining and can spread to nearby organs. This type of cancer is closely related to ovarian cancer in terms of its behavior and characteristics.

Trial ID:
2024-516066-11-00
Protocol code:
AGO-OVAR 28
NCT ID:
NCT05009082
Trial Phase:
Therapeutic confirmatory (Phase III)

Other Trials to Consider

  • Phase 3 Study of LY4170156 (Sofetabart Mipitecan) with drug combination in platinum‑resistant and platinum‑sensitive ovarian cancer patients

    Recruiting

    3 1 1 1
    Austria Belgium Czechia Denmark France Germany +9
  • A study of sacituzumab tirumotecan and bevacizumab in patients with newly diagnosed advanced ovarian cancer following first-line platinum-based chemotherapy

    Recruiting

    3 1 1 1
    Investigated diseases:
    Austria Belgium Czechia Denmark Finland France +9