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About Us

Affymax Milestones

  • 2001
    Incorporated in July in Delaware
  • 2003
    Lead compound, peginesatide, selected for clinical development
  • 2004
    Peginesatide entered the clinic
  • 2006
    Worldwide collaboration for peginesatide established with Takeda Pharmaceutical Company Limited
  • 2006
    IPO in December, Nasdaq symbol AFFY
  • 2007
    Phase 3 trials for peginesatide initiated in chronic kidney disease
  • 2008
    Enrollment completed in
    Phase 3 trials for peginesatide in chronic kidney disease
  • 2010
    Completion of treatment and follow-up in Phase 3 trials
  • 2010
    Data from Phase 3 trials for peginesatide in chronic kidney disease announced
  • 2011
    Peginesatide NDA accepted for review by the FDA

Corporate Overview

Affymax is a biopharmaceutical company committed to developing novel drugs to improve the treatment of serious and often life-threatening conditions. The company’s first product candidate, peginesatide (formerly known as Hematide™), has been investigated in Phase 3 trials for the potential treatment of anemia associated with chronic kidney disease (CKD). A New Drug Application (NDA) for peginesatide for the treatment of anemia associated with CKD in adult patients on dialysis is currently being reviewed by the U.S. Food and Drug Administration (FDA).

Anemia is a serious condition in which blood is deficient in red blood cells and hemoglobin. It is common in patients with CKD, cancer, heart failure, inflammatory diseases and other critical illnesses, as well as in the elderly. If left untreated, anemia may lead to chronic fatigue or increase the risk of other diseases or death.