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)
Duration of Progression-Free Survival (PFS) by Blinded Independent Radiology Committee (BIRC) — Up to 32 months Duration of PFS was defined as the time from randomization to the earlier of either the date of radiographic progression per BIRC or the date of death due to any cause. PFS (months) = (earliest date of progression, death, censoring - date of randomization + 1)/30.4375. PFS was determined as per Response Evaluation Criteria in Solid Tumors version (RECIST) v1.1.
Trial sites (159)
Facility
City
Region
Status
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.
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.
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