Study Description
Screening
Study Centers
Contact/Consent
Kidney Cancer Disease Study CRAD001L2201
The purpose of this medical research is to study the effects of combining a Novartis investigational drug with an existing therapy, when treating people with metastatic clear cell carcinoma of the kidney (Kidney Cancer). An “investigational drug” is a drug that is being tested and is not approved for sale in the United States by the U.S. Food and Drug Administration (FDA).
Trial phase:
Phase 2
Participation Duration:
Participants will be required to visit their study site every two weeks for approximately two years. One group will be required to inject themselves three times a week and return to the study site every two weeks for an additional infusion treatment. Another group, will be required to take two tablets every day and return to the site every two weeks for an additional infusion treatment.
Protocol Number:
CRAD001L2201
The next step is to see if you (or the participant) meet the
basic criteria required for participation in this clinical trial.
Please fill out the questionnaire below to see if you (or the
participant) may be suitable for the clinical trial. Your answers to
these questions are not retained by this system. You must answer the
questions below for yourself, or, you must be the legally authorized
representative of the potential participant in order to answer the
questions on their behalf. If you (or the participant) do not meet
the preliminary qualifications, you may search for other clinical
trials of interest or sign up to the Mailing List.
Answers to all questions are required to determine if you meet
the preliminary qualifications for the study.
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