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Tyrosine Kinase Inhibitor
Cabozantinib vs Sunitinib for Kidney Cancer
Phase 2
Waitlist Available
Led By Matthew T Campbell
Research Sponsored by M.D. Anderson Cancer Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
The subject has organ and marrow function and laboratory values as follows within 4 days before the first dose of cabozantinib or sunitinib: a.The ANC >/= 1500/mm^3 without colony stimulating factor support; b.White blood cell count >/= 2500/mm^3 (>/= 2.5 GI/L). c.Platelets >/=100,000/mm^3; d.Hemoglobin >/= 9 g/dL; e. Bilirubin </= 1.5 x the ULN. For subjects with known Gilbert's disease, bilirubin </= 3.0 mg/dL; f.Serum albumin >/= 2.8 g/dl g.Serum creatinine </= 2.0 X ULN or calculated creatinine clearance >/= 30 mL/min (>/= 0.5 mL/sec) using the Cockcroft-Gault equation: Males: (140 - age) x weight (kg)/(serum creatinine [mg/dL] × 72) Females: [(140 - age) x weight (kg)/(serum creatinine [mg/dL] × 72)] × 0.85 h.Alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase (ALP) </= 3 X upper limit of normal (ULN). ALP </= 5 X ULN with documented bone metastases. i.Urine protein/creatinine ratio (UPCR) </= 1 mg/mg (</= 113.2 mg/mmol);
The subject is >/=18 years old on the day of consent;
Must not have
The subject has a variant histology that includes renal medullary carcinoma or collecting duct renal cell carcinoma. Any clear cell component in the tumor will lead to exclusion.
Major surgery (eg, GI surgery, removal or biopsy of brain metastasis) within 8 weeks before first dose of study treatment. Complete wound healing from major surgery must have occurred 1 month before first dose and from minor surgery (eg, simple excision, tooth extraction) at least 10 days before first dose. Subjects with clinically relevant ongoing complications from prior surgery are not eligible.
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from randomization up to the time of disease progression or death up to two years
Awards & highlights
No Placebo-Only Group
Summary
This trial will compare the safety and effectiveness of two drugs for kidney cancer.
Who is the study for?
This trial is for adults with a specific type of kidney cancer that has spread and may have had one prior treatment excluding certain drugs. They should be in good physical condition, not pregnant, able to follow the study plan, and willing to use contraception. People with certain medical conditions or who've taken specific treatments recently can't join.
What is being tested?
The trial aims to compare the safety and effectiveness of two FDA-approved drugs for advanced kidney cancer: cabozantinib and sunitinib malate. Participants will receive either drug to determine which works better against this particular form of cancer.
What are the potential side effects?
Potential side effects include high blood pressure, fatigue, diarrhea, hand-foot syndrome (redness and pain on palms or soles), mouth sores, altered taste sensation, nausea/vomiting, decreased appetite/weight loss, hair color changes.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
Before starting the medication, your blood and organ function need to be within certain levels. For example, your white blood cell count needs to be at least 2500/mm^3, and your bilirubin levels need to be below a certain number.
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I am 18 years old or older.
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I can take care of myself but might not be able to do heavy physical work.
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I agree to use two forms of birth control during the study and for 4 months after.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
My kidney cancer is a specific type without any clear cell components.
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I have fully healed from any major surgery 1 month before starting the treatment and have no ongoing complications.
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I have previously been treated with drugs that stop the formation of new blood vessels in tumors, including cabozantinib.
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I haven't had recent radiation for bone metastasis or other radiation treatments.
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I have had brain metastases treated and stable for 4 weeks, and I'm not on steroids.
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I do not have serious heart issues, uncontrolled high blood pressure, or recent major cardiovascular events.
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I have serious stomach or intestine problems, including recent surgery complications.
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I have not had significant bleeding or serious wounds, and my liver and thyroid function are stable.
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My heart's electrical activity, measured by QTcF, is not over 500 ms.
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I cannot swallow pills.
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I need ongoing treatment with certain strong medications.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ from randomization to death or last contact if still alive up to two years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from randomization to death or last contact if still alive up to two years
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Progression-Free Survival (PFS) Evaluated Using RECIST 1.1 Criteria
Secondary study objectives
Adverse Event Rates
Objective Response Rate (ORR) Evaluated Using RECIST 1.1 Criteria
Overall Survival (OS)
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Group I: Group 2 (sunitinib malate)Experimental Treatment1 Intervention
Participants receive sunitinib malate PO QD on days 1-28. Courses repeat every 6 weeks in the absence of disease progression or unacceptable toxicity.
Group II: Group 1 (cabozantinib)Experimental Treatment1 Intervention
Participants receive cabozantinib PO QD on days 1-42. Courses repeat every 6 weeks in the absence of disease progression or unacceptable toxicity.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Cabozantinib
2020
Completed Phase 2
~1760
Sunitinib Malate
2008
Completed Phase 3
~3070
Find a Location
Who is running the clinical trial?
M.D. Anderson Cancer CenterLead Sponsor
3,059 Previous Clinical Trials
1,800,636 Total Patients Enrolled
National Cancer Institute (NCI)NIH
13,906 Previous Clinical Trials
41,012,000 Total Patients Enrolled
ExelixisIndustry Sponsor
120 Previous Clinical Trials
20,098 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My kidney cancer is a specific type without any clear cell components.I am on certain blood thinners or platelet inhibitors, but not for brain metastases.I have fully healed from any major surgery 1 month before starting the treatment and have no ongoing complications.I understand the study requirements and have signed the consent form.Your blood clotting tests are significantly higher than the normal range within 7 days before starting the study treatment.You have had a recent assessment of all known disease sites using scans like CT, MRI, or bone scan within the last 28 days before starting the medication.Before starting the medication, your blood and organ function need to be within certain levels. For example, your white blood cell count needs to be at least 2500/mm^3, and your bilirubin levels need to be below a certain number.I have previously been treated with drugs that stop the formation of new blood vessels in tumors, including cabozantinib.I am 18 years old or older.My kidney cancer is a special type and I've had limited or specific previous treatments.I can take care of myself but might not be able to do heavy physical work.I have had brain metastases treated and stable for 4 weeks, and I'm not on steroids.I do not have serious heart issues, uncontrolled high blood pressure, or recent major cardiovascular events.I haven't had recent radiation for bone metastasis or other radiation treatments.I have serious stomach or intestine problems, including recent surgery complications.I have not had significant bleeding or serious wounds, and my liver and thyroid function are stable.I cannot swallow pills.I haven't had any cancer except for minor skin cancer or low-risk tumors in the last 2 years.My heart's electrical activity, measured by QTcF, is not over 500 ms.I have recovered from previous treatment side effects, or they are minor and stable.I agree to use two forms of birth control during the study and for 4 months after.I am not pregnant and can potentially become pregnant.I need ongoing treatment with certain strong medications.The doctor has confirmed that you have a disease that can be measured using specific guidelines.
Research Study Groups:
This trial has the following groups:- Group 1: Group 2 (sunitinib malate)
- Group 2: Group 1 (cabozantinib)
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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