U.S. Food and Drug Administration approval summary: Eltrombopag for the treatment of pediatric patients with chronic immune (idiopathic) thrombocytopenia

Pediatr Blood Cancer. 2017 Dec;64(12). doi: 10.1002/pbc.26657. Epub 2017 Jun 19.

Abstract

The U.S. Food and Drug Administration (FDA) approved eltrombopag for pediatric patients with chronic immune (idiopathic) thrombocytopenia (ITP) ages ≥6 on June 11, 2015, and ages ≥1 on August 24, 2015. Approval was based on the FDA review of two randomized trials that included 159 pediatric patients with chronic ITP who had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. This manuscript describes the basis for approval of these applications. The FDA concluded that eltrombopag has shown efficacy and a favorable benefit to risk profile for pediatric patients with chronic ITP.

Keywords: Promacta; eltrombopag; immune thrombocytopenic purpura; pediatric.

MeSH terms

  • Adolescent
  • Benzoates / administration & dosage
  • Benzoates / therapeutic use*
  • Child
  • Child, Preschool
  • Chronic Disease
  • Drug Approval
  • Female
  • Humans
  • Hydrazines / administration & dosage
  • Hydrazines / therapeutic use*
  • Infant
  • Male
  • Pyrazoles / administration & dosage
  • Pyrazoles / therapeutic use*
  • Thrombocythemia, Essential / drug therapy*
  • United States
  • United States Food and Drug Administration*

Substances

  • Benzoates
  • Hydrazines
  • Pyrazoles
  • eltrombopag