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Clinical Trials in the UK / NCT03937219
Active, not recruiting Phase 3

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

NCT03937219 · tracked via the Priya Life Science UK tracker
Sponsor
Exelixis
Phase
Phase 3
Started
2019-06-25
Last updated
2025-09-10

Condition(s) studied

Renal Cell Carcinoma

Investigational drug(s) / intervention(s)

CabozantinibNivolumabIpilimumabCabozantinib-matched placebo

Cabozantinib: Specified dose on specified days.

Nivolumab: Specified dose on specified days.

Ipilimumab: Specified dose on specified days.

Cabozantinib-matched placebo: Specified dose on specified days.

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * 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. Exclusion Criteria: * 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. * Concomitant anticoagulation with oral anticoagulants or platelet inhibitors. * Administration of a live, attenuated vaccine within 30 days prior to randomization. * 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. * 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.

Primary outcome measure(s)

Trial sites (159)

FacilityCityRegionStatus
Exelixis Clinical Site #116 La Jolla California
Exelixis Clinical Site #166 Orange California
Exelixis Clinical Site #29 Boca Raton Florida
Exelixis Clinical Site #44 Miami Florida
Exelixis Clinical Site #3 Atlanta Georgia
Exelixis Clinical Site #95 Chicago Illinois
Exelixis Clinical Site #69 Scarborough Maine
Exelixis Clinical Site #58A Baltimore Maryland
Exelixis Clinical Site #7B Boston Massachusetts
Exelixis Clinical Site #7A Boston Massachusetts
Exelixis Clinical Site #7C Boston Massachusetts
Exelixis Clinical Site #6 Burlington Massachusetts
Exelixis Clinical Site #15 Detroit Michigan
Exelixis Clinical Site #24 Kansas City Missouri
Exelixis Clinical Site #4 St Louis Missouri
Exelixis Clinical Site #2 Omaha Nebraska
Exelixis Clinical Site #159 New York New York
Exelixis Clinical Site #8 New York New York
Exelixis Clinical Site #19 Syracuse New York
Exelixis Clinical Site #101 Charlotte North Carolina
Exelixis Clinical Site #107 Portland Oregon
Exelixis Clinical Site #12 Pittsburgh Pennsylvania
Exelixis Clinical Site #102 Charleston South Carolina
Exelixis Clinical Site #5 Myrtle Beach South Carolina
Exelixis Clinical Site #10 Nashville Tennessee
Exelixis Clinical Site #38 Nashville Tennessee
Exelixis Clinical Site #64 Fairfax Virginia
Exelixis Clinical Site #57 Seattle Washington
Exelixis Clinical Site #1 Spokane Washington
Exelixis Clinical Site #13 Madison Wisconsin
Exelixis Clinical Site #153 Pilar Buenos Aires
Exelixis Clinical Site #109 Rosario Santa Fe Province
Exelixis Clinical Site #73 San Miguel de Tucumán Tucumán Province
Exelixis Clinical Site #54 Buenos Aires Argentina
Exelixis Clinical Site #63 CABA Argentina
Exelixis Clinical Site #110 Ciudad Autonoma de Buenos Aire Argentina
Exelixis Clinical Site #120 Córdoba Argentina
Exelixis Clinical Site #32 Albury New South Wales
Exelixis Clinical Site #35 Kogarah New South Wales
Exelixis Clinical Site #27 North Ryde New South Wales

+ 119 more sites — see the full list on the official registry below.

On this site

📄 Cabometyx (cabozantinib) drug profile → 📄 Opdivo (nivolumab) drug profile →

More Exelixis trials in the UK

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03937219 on ClinicalTrials.gov ↗ ← All trials in the UK