Study Description
Screening
Study Centers
Contact/Consent
Metastatic Melanoma
Metastatic melanoma is the most advanced stage melanoma--a type of skin cancer. These cancer cells can become malignant and grow uncontrollably. This creates a fast-growing mass of cells, called a tumor.
Novartis is seeking people to participate in a clinical trial(s) testing the safety
and effectiveness of Novartis products. Novartis recommends that you consult your
doctor before participating in a clinical trial.
For more information about clinical trial participation, click here. Also, for additional information
about how Novartis helps to protect the privacy of the personal information that you provide to us, please
see the Novartis Privacy Policy.
Please review the details of the clinical trial(s) listed below and click on the one that you feel best suits
your (or the participant's) condition.
Malignant Melanoma Study - US255
Novartis Oncology is supporting a clinical study that is being sponsored and conducted by Dr. F. Stephen Hodi of the Dana-Farber Cancer Institute, to find out if a Novartis study drug is safe and effective for people with metastatic acral lentiginous melanoma. An "investigational drug" is a drug that is being clinically tested and is not approved for sale or use in the United States by the Food and Drug Administration (FDA), for the indication in which it is being studied.
Trial phase: Phase 2
Participation Duration: Participants will be asked to visit the study center a predetermined number of times over the course of a one year period.
Protocol Number: CSTI571BUS255
Metastatic Melanoma Study - B2301
A randomized, phase III, open label, multi-center, two-arm study to compare the efficacy of a Novartis investigational drug versus and exsisting therapy in the treatment of patients with metastatic and/or inoperable melanoma harboring a c-Kit mutation. An "investigational drug" is a drug that is being clinically tested and is not approved for sale or use in the United States by the Food and Drug Administration (FDA), for the indication in which it is being studied.
Trial phase: Phase 3
Participation Duration: Participation in this trial would include coming to the doctors office every 3 weeks, then every 3 weeks from then on. Each visit should take about 4 hours.
Protocol Number: CAMN107B2301
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