Pembrolizumab is a highly selective IgG4-kappa humanized monoclonal antibody against PD-1 receptors. It was generated by grafting the variable sequences of a very high-affinity mouse antihuman PD-1 antibody onto a human IgG4-kappa isotype containing a stabilizing S228P Fc mutation. It contains 32 cysteine residues and the complete folded molecule includes 4 disulfide linkages as interchain bonds and 23 interchain bonds. It was developed by Merck & Co and first approved for the treatment of metastatic malignant melanoma by the FDA on September 4, 2014, becoming the first approved therapy against PD-1. In the time since its initial approval, pembrolizumab has been granted approval in the treatment of a wide variety of cancers.
Pembrolizumab is indicated for the following conditions:
For all approved adult indications, pembrolizumab may be used for an additional 6 weeks at 400mg weekly.
Recruiting, Providence, Rhode Island, United States
Recrutiing, Philadelphia, Pennsylvania, United States
University of Colorado Health Sciences Center (UCHSC), Aurora, Colorado, United States
Western Regional Medical Center/Cancer Treatment Center of America, Goodyear, Arizona, United States
Sidney Kimmel Cancer Center at Thomas Jefferson University, Philadelphia, Pennsylvania, United States
Abramson Cancer Center of the University of Pennsylvania, Philadelphia, Pennsylvania, United States
H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, United States
OHSU Knight Cancer Institute, Portland, Oregon, United States
Saint Louis University Hospital, Saint Louis, Missouri, United States
Hartford HealthCare, Hartford, Connecticut, United States
Dana-Farber Cancer Institute, Boston, Massachusetts, United States
Mayo Clinic Cancer Center, Phoenix, Arizona, United States
Abramson Cancer Center of the University of Pennsylvania, Philadelphia, Pennsylvania, United States
Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia
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