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NCT03937219Active, not recruitingPhase 3

Study of Cabozantinib in Combination With Nivolumab and Ipilimumab in Patients With Previously Untreated Advanced or Metastatic Renal Cell Carcinoma

A Randomized, Double-Blind, Controlled Phase 3 Study of Cabozantinib in Combination With Nivolumab and Ipilimumab Versus Nivolumab and Ipilimumab in Subjects With Previously Untreated Advanced or Metastatic Renal Cell Carcinoma of Intermediate or Poor Risk

Source: ClinicalTrials.gov · Last updated 20 Oct 2026

Brief summary (registry, in English)

This is a multicenter, randomized, double-blinded, controlled Phase 3 trial of cabozantinib in combination with nivolumab and ipilimumab versus nivolumab and ipilimumab in combination with matched placebo. Approximately 840 eligible subjects with intermediate- or poor-risk advanced or metastatic RCC by IMDC criteria will be randomized in a 1:1 ratio at approximately 180 sites.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
855 (actual)
First submitted
2 May 2019
Start date
25 Jun 2019
Primary completion date
31 Jan 2022
Lead sponsor
Exelixis
NCT number
NCT03937219
EU CT number
2024-515616-47-00
EudraCT number
2018-004567-31

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 855
  • From 25 Jun 2019 to the primary completion date, 31 Jan 2022
  • 151 sites in 25 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior systemic anticancer therapy for unresectable locally advanced or metastatic RCC including investigational agents.
  • Radiation therapy for bone metastasis within 2 weeks, any other radiation therapy within 4 weeks prior to randomization.
  • Known brain metastases or cranial epidural disease unless adequately treated with radiotherapy and stable for at least 4 weeks prior to randomization.
  • Administration of a live, attenuated vaccine within 30 days prior to randomization.
  • Other clinically significant disorders such as:
    • Autoimmune disease that has been symptomatic or required treatment within the past two years from the date of randomization.
    • Any condition requiring systemic treatment with either corticosteroids (\> 10 mg daily prednisone equivalent) or other immunosuppressive medications within 14 days of randomization.
    • Active infection requiring systemic treatment. Acute or chronic hepatitis B or C infection, known human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS)-related illness, or known positive test for tuberculosis infection where there is clinical or radiographic evidence of active myobacterial infection.
    • Known history of COVID-19 unless the subject has clinically recovered from the disease at least 30 days prior to randomization.
  • Major surgery (eg, nephrectomy, GI surgery, removal or biopsy of brain metastasis) within 4 weeks prior to randomization. Minor surgeries within 10 days prior to randomization. Subjects must have complete wound healing from major or minor surgery before randomization.
  • Any other active malignancy at time of randomization or diagnosis of another malignancy within 3 years prior to randomization that requires active treatment, except for locally curable cancers that have been apparently cured, such as basal or squamous cell skin cancer, superficial bladder cancer, or carcinoma in situ of the prostate, cervix, or breast.

Other illness

  • Uncontrolled, significant intercurrent or recent illness including, but not limited to serious cardiovascular disorders (including uncontrolled hypertension defined as sustained blood pressure (BP) \> 150 mm Hg systolic or \> 90 mm Hg diastolic despite optimal antihypertensive treatment), GI disorders associated with high risk for perforation or fistula formation, tumors invading GI tract, bowel obstruction, intra-abdominal abscess, clinically significant bleeding events, cavitating pulmonary lesions, or lesions invading major pulmonary blood vessels.

Lab values

  • Concomitant anticoagulation with oral anticoagulants or platelet inhibitors.

Who the study is looking for

  • Histologically confirmed advanced (not amenable to curative surgery or radiation therapy) or metastatic (AJCC Stage IV) renal cell carcinoma with a clear-cell component.
  • Intermediate- or poor-risk RCC as defined by International Metastatic RCC Database Consortium (IMDC) criteria.
  • Measurable disease per RECIST 1.1 as determined by the Investigator. Measurable disease must be outside the radiation field if radiation therapy was previously administered.
  • Karnofsky Performance Status (KPS) ≥ 70%.
  • Adequate organ and marrow function.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (151)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
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Buenos AiresArgentinaUnknown status
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CABAArgentinaUnknown status
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Ciudad Autonoma de Buenos AireArgentinaUnknown status
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CórdobaArgentinaUnknown status
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PilarArgentinaUnknown status
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RosarioArgentinaUnknown status
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San Miguel de TucumánArgentinaUnknown status
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LinzAustriaUnknown status
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SalzburgAustriaUnknown status
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ViennaAustriaUnknown status
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Wiener NeustadtAustriaUnknown status
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AdelaideAustraliaUnknown status
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AlburyAustraliaUnknown status
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BallaratAustraliaUnknown status
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Box HillAustraliaUnknown status
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KogarahAustraliaUnknown status
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North AdelaideAustraliaUnknown status
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North RydeAustraliaUnknown status
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South BrisbaneAustraliaUnknown status
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SubiacoAustraliaUnknown status
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SydneyAustraliaUnknown status
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WoolloongabbaAustraliaUnknown status
Institut Jules Bordet
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AnderlechtBelgiumCompleted
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BarretosBrazilUnknown status
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Belo HorizonteBrazilUnknown status
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CuritibaBrazilUnknown status
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Porto AlegreBrazilUnknown status
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Porto AlegreBrazilUnknown status
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Porto AlegreBrazilUnknown status
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São José do Rio PretoBrazilUnknown status
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São PauloBrazilUnknown status
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São PauloBrazilUnknown status
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CalgaryCanadaUnknown status
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MontrealCanadaUnknown status
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OttawaCanadaUnknown status
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TorontoCanadaUnknown status
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WinnipegCanadaUnknown status
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SantiagoChileUnknown status
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SantiagoChileUnknown status
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TemucoChileUnknown status
Fakultni Nemocnice Hradec Kralove
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Novy Hradec KraloveCzechiaCompleted
Fakultni nemocnice v Motole
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PragueCzechiaCompleted
Fakultni Thomayerova nemocnice
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Prague 4CzechiaCompleted
Universitaetsklinikum Carl Gustav Carus Dresden an der Technischen Universitaet Dresden AöR
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DresdenGermanyCompleted
National Center for Tumor Diseases (NCT) Heidelberg
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HeidelbergGermanyCompleted
Universitaetsklinikum Jena KöR
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JenaGermanyCompleted
Universitaetsmedizin der Johannes Gutenberg-Universitaet Mainz KöR
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MainzGermanyCompleted
Universitaetsklinikum Muenster AöR
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MuensterGermanyCompleted
Universitaetsklinikum Tuebingen AöR
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TuebingenGermanyCompleted
Hospital Clinic de Barcelona
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BarcelonaSpainActive, not recruiting
Hospital Universitari Vall d'Hebron
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BarcelonaSpainActive, not recruiting
Hospital Universitario Reina Sofia
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CórdobaSpainActive, not recruiting
Hospital Clínico San Carlos
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MadridSpainActive, not recruiting
Hospital General Universitario Gregorio Marañón
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MadridSpainActive, not recruiting
Hospital Universitario 12 de Octubre
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MadridSpainActive, not recruiting
Hospital Universitario HM Sanchinarro
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MadridSpainActive, not recruiting
Hospital Universitario Central De Asturias
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OviedoSpainActive, not recruiting
Clínica Universidad de navarra
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PamplonaSpainActive, not recruiting
Complexo Hospitalario Universitario De Santiago
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Santiago de CompostelaSpainActive, not recruiting
Fundación Instituto Valenciano de Oncología
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ValenciaSpainActive, not recruiting
HUS-Yhtymae
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HelsinkiFinlandCompleted
Pirkanmaan hyvinvointialue
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TampereFinlandCompleted
Turku University Hospital
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TurkuFinlandCompleted
Centre hospitalier Universitaire de Bordeaux
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BordeauxFranceCompleted
Clinique Victor Hugo
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Le MansFranceCompleted
Centre Leon Berard
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LyonFranceCompleted
Centre Hospitalier Universitaire De Montpellier
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Montpellier Cedex 5FranceCompleted
Centre Antoine Lacassagne
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Nice Cedex 2FranceCompleted
Institut Godinot
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ReimsFranceCompleted
Les Hopitaux Universitaires De Strasbourg
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Strasbourg CedexFranceCompleted
Oncopole Claudius Regaud
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Toulouse Cedex 9FranceCompleted
Institut De Cancerologie De Lorraine
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Vandouvre Les NancyFranceCompleted
Institut Gustave Roussy
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VillejuifFranceCompleted
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CambridgeUnited KingdomUnknown status
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GlasgowUnited KingdomUnknown status
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LondonUnited KingdomUnknown status
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LondonUnited KingdomUnknown status
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ManchesterUnited KingdomUnknown status
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Hong KongHong Kong SAR ChinaUnknown status
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ShatinHong Kong SAR ChinaUnknown status
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TuenmenHong Kong SAR ChinaUnknown status
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BudapestHungaryUnknown status
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PécsHungaryUnknown status
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BeershebaIsraelUnknown status
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HaifaIsraelUnknown status
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JerusalemIsraelUnknown status
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Kfar SabaIsraelUnknown status
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Petah TikvaIsraelUnknown status
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Ramat GanIsraelUnknown status
Azienda Unita Sanitaria Locale Della Romagna
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FaenzaItalyActive, not recruiting
Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori" - IRST S.r.l
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MeldolaItalyActive, not recruiting
Azienda Ospedaliero - Universitaria di Modena
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ModenaItalyActive, not recruiting
Istituto Oncologico Veneto
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PadovaItalyActive, not recruiting
Istituti Clinici Scientifici Maugeri S.p.A. Societa' Benefit In Forma Abbreviata Istituti Clinici Scientifici Maugeri S.p.A. Sb O Anche Ics Maugeri S.p.A. Sb O Maugeri S.p.A. Sb
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PaviaItalyActive, not recruiting
Azienda Ospedaliera S Maria Di Terni
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TerniItalyActive, not recruiting
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Seongnam-siSouth KoreaUnknown status
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SeoulSouth KoreaUnknown status
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SeoulSouth KoreaUnknown status
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SeoulSouth KoreaUnknown status
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AguascalientesMexicoUnknown status
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LeónMexicoUnknown status
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Mexico CityMexicoUnknown status
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MonterreyMexicoUnknown status
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Oaxaca CityMexicoUnknown status
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QuerétaroMexicoUnknown status
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QuerétaroMexicoUnknown status
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ZapopanMexicoUnknown status
Amsterdam UMC Stichting
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AmsterdamNetherlandsCompleted
Erasmus Universitair Medisch Centrum Rotterdam (Erasmus MC)
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RotterdamNetherlandsCompleted
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HamiltonNew ZealandUnknown status
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NewtownNew ZealandUnknown status
Wojewodzki Szpital Specjalistyczny W Bialej Podlaskiej
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Biala PodlaskaPolandActive, not recruiting
Centrum Onkologii Im. Prof. Franciszka Lukaszczyka W Bydgoszczy
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BydgoszczPolandActive, not recruiting
Copernicus Podmiot Leczniczy Sp. z o.o
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GdanskPolandActive, not recruiting
Europejskie Centrum Zdrowia Otwock Sp. Z.o.o.
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OtwockPolandActive, not recruiting
Med Polonia Sp z o.o.
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PoznanPolandActive, not recruiting
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SingaporeSingaporeUnknown status
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SingaporeSingaporeUnknown status
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TaichungTaiwanUnknown status
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TaipeiTaiwanUnknown status
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TaoyuanTaiwanUnknown status
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AtlantaUnited StatesUnknown status
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BaltimoreUnited StatesUnknown status
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Boca RatonUnited StatesUnknown status
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BostonUnited StatesUnknown status
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BostonUnited StatesUnknown status
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BostonUnited StatesUnknown status
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BurlingtonUnited StatesUnknown status
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CharlestonUnited StatesUnknown status
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CharlotteUnited StatesUnknown status
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ChicagoUnited StatesUnknown status
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DetroitUnited StatesUnknown status
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FairfaxUnited StatesUnknown status
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Kansas CityUnited StatesUnknown status
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La JollaUnited StatesUnknown status
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MadisonUnited StatesUnknown status
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MiamiUnited StatesUnknown status
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Myrtle BeachUnited StatesUnknown status
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NashvilleUnited StatesUnknown status
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NashvilleUnited StatesUnknown status
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New YorkUnited StatesUnknown status
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New YorkUnited StatesUnknown status
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OmahaUnited StatesUnknown status
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OrangeUnited StatesUnknown status
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PittsburghUnited StatesUnknown status
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PortlandUnited StatesUnknown status
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ScarboroughUnited StatesUnknown status
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SeattleUnited StatesUnknown status
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SpokaneUnited StatesUnknown status
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St LouisUnited StatesUnknown status
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SyracuseUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.