Trial Search Results

Study of Nivolumab (BMS-936558) vs. Everolimus in Pre-Treated Advanced or Metastatic Clear-cell Renal Cell Carcinoma (CheckMate 025)

The purpose of the study is to compare the clinical benefit, as measured by duration of overall survival, of Nivolumab vs. Everolimus in subjects with advanced or metastatic clear-cell renal cell carcinoma who have received prior anti-angiogenic therapy

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Bristol-Myers Squibb

Collaborator: Ono Pharmaceutical Co. Ltd

Stanford Investigator(s):


  • Biological: Nivolumab
  • Drug: Everolimus


Phase 3


For more information regarding BMS clinical trial participation, please visit

Inclusion Criteria:

   - Men & women ≥18 years of age

   - Histologic confirmation of renal cell carcinoma (RCC) with clear-cell component

   - Advanced/metastatic RCC

   - Measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST) 1.1

   - Received 1 or 2 prior anti-angiogenic therapy regimens in advanced or metastatic

   - No more than 3 total prior systemic treatment regimens in the advanced or metastatic
   setting, and evidence of progression on or after last treatment regimen received and
   within 6 months of enrollment

   - Karnofsky Performance Score ≥70%

Exclusion Criteria:

   - Any Central Nervous System (CNS) metastases or history of CNS metastases

   - Prior therapy with an Mammalian target of rapamycin (mTOR) inhibitor

   - Any active known or suspected autoimmune disease

   - Uncontrolled adrenal insufficiency

   - Active chronic liver disease

   - Prior malignancy active within past 3 years, except for locally curable cancers

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study


Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Not Recruiting