Trial Search Results

Adjuvant Axitinib Therapy of Renal Cell Cancer in High Risk Patients

The purpose of this trial is to determine if adjuvant therapy with axitinib will prevent or delay the recurrence of renal cell cancer after surgery to remove the primary tumor in high risk patients.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

SFJ Pharma Ltd. II

Collaborator: SFJ Pharmaceuticals, Inc.

Stanford Investigator(s):

Intervention(s):

  • Drug: Axitinib
  • Drug: Placebo

Phase:

Phase 3

Eligibility


Inclusion Criteria:

Patients must be treated by nephrectomy and patients must meet all of the following
inclusion criteria to be eligible for enrollment into the trial:

   1. Patients must have no evidence of macroscopic residual disease or metastatic disease.

   2. Male or female, age >=18 years (age >=20 years in Japan, Korea and Taiwan).

   3. Patients must be diagnosed with one of the following based on American Joint Committee
   on Cancer (AJCC) TNM staging version 2010, Eastern Collaborative Oncology Group (ECOG)
   performance status (PS):

      - pT2, pN0 or pNx, M0 and ECOG PS 0-1

      - pT3, pN0 or pNx, M0 and ECOG PS 0-1

      - pT4, pN0 or pNx, M0 and ECOG PS 0-1

      - Any pT, pN1, M0 and ECOG PS 0-1

   4. Patients must have histologically confirmed preponderant, defined as >50%, clear cell
   RCC.

   5. Patients must not have received any previous systemic (includes chemotherapeutic,
   hormonal, or immunotherapeutic) treatment for RCC.

   6. Patients must not have received any previous anti angiogenic treatment.

   7. Patients must have adequate organ function.

Exclusion Criteria

   1. Histologically undifferentiated carcinomas, sarcomas, collecting duct carcinoma,
   lymphoma, or patients with any metastatic renal sites.

   2. National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE)
   Grade 3 hemorrhage <4 weeks of date of randomization.

   3. Diagnosis of any non-RCC malignancy within the 5 years from date of randomization,
   except basal cell carcinoma, squamous cell skin cancer, or in situ carcinoma of the
   cervix uteri that has been adequately treated with no evidence of recurrent disease
   for 12 months.

   4. Any of the following within the 12 months prior to study drug administration:
   myocardial infarction, uncontrolled angina, coronary/peripheral artery bypass graft,
   symptomatic congestive heart failure, cerebrovascular accident or transient ischemic
   attack and 6 months for deep vein thrombosis or pulmonary embolism.

   5. Gastrointestinal abnormalities

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
CCTO
650-498-7061
Not Recruiting