Ipilimumab is a fully humanized IgG1 monoclonal antibody that blocks cytotoxic T lymphocyte antigen-4 (CTLA-4). Blocking CTLA-4 removes an inhibitory signal from reducing the activity of T lymphocytes. Ipilimumab was developed by Bristol-Myers Squibb and Medarex.
Ipilimumab was granted FDA approval on 25 March 2011.
Ipilimumab is indicated in the following cancerous conditions:
Melanoma
Renal Cell Carcinoma (RCC)
Colorectal Cancer
Hepatocellular Carcinoma
Non-Small Cell Lung Cancer (NSCLC)
Malignant Pleural Mesothelioma
Esophageal Cancer
- Treatment of adult patients with unresectable advanced or metastatic esophageal squamous cell carcinoma, as first line treatment in combination with nivolumab
Stanford Cancer Institute, Stanford, California, United States
Memorial Sloan Kettering Cancer Center, New York, New York, United States
Gabrail Cancer Center, Canton, Ohio, United States
University of Kansas Cancer Center, Westwood, Kansas, United States
Icahn School Of Medicine at Mount Sinai, New York, New York, United States
University Hospital Zurich, Zurich, Switzerland
IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy
Clinica Universidad de Navarra, Pamplona, Spain
H. C. U. de Valladolid, Valladolid, Spain
H. U. Virgen de la Victoria, Malaga, Spain
Hospital La Paz, Madrid, Spain
Medical Oncology and Immunotherapy Unit, University Hospital of Siena, Siena, Italy
Mount Vernon Hospital, Northwood, United Kingdom
Local Institution, Truro, United Kingdom
Local Institution, Shanghai, China
Local Institution, Guangzhou, Guangdong, China
Illinois CancerCare-Macomb, Macomb, Illinois, United States
Carle Physician Group-Mattoon/Charleston, Mattoon, Illinois, United States
McFarland Clinic - Ames, Ames, Iowa, United States
University of California, San Francisco, San Francisco, California, United States
Stay informed with timely notifications on clinical trials, regulatory changes, and research advancements related to this medication.