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ECOG E1609; A Phase III Randomized Study of Adjuvant Ipilimumab Anti-CTLA4 Therapy Versus High-Dose Interferon a2b for Resected High Risk Melanoma

Objective
This is a clinical trial of ipilimumab that will be administered by IV which is investigational and interferon Alfa-2b that will be administered by IV and is standard of care.
IRB Protocol Number
11-0999
Principal Investigator(s)
KARL LEWIS

Cancer Trials

  • Melanoma (Except Eye)
Sponsor(s)
ECOG
Contact
COURTNEY VON BERGEN at
Eligibility and Other Participant Information
What To Expect : A screening period to determine eligibility. A treatment period that can last up to 12 to 18 months. A follow up period will consist of clinic visits. // Eligibility criteria include but are not limited to 18 years or older with melanoma.

Location

  • ST. MARYS HOSPITAL - G.J.