The FDA Has Approved a New Sickle Cell Drug for the First Time in 20 Years

Sickle cell disease has long plagued minorities—particularly African Americans and Latinos—with painful and sometimes debilitating crises. The inherited lifelong disorder, due to abnormal hemoglobin, has perplexed doctors as though many are skilled at identifying the disease, success has been limited as far as treating the resulting crises once they arise.
There was little hope, until now. Endari, a drug that reduces the complications associated with sickle cell, has just been approved by the U.S. Food and Drug Administration. It is the first drug approved for the blood disorder in the past 20 years.
“I am hoping we are finally seeing channels opening, and that this will be the first of many new drugs to hit the market [for sickle cell disease],” said Dr. Alexis A. Thompson. Dr. Thompson is the head of the Hematology Section and Director of the Comprehensive Thalassemia Program at the Ann and Robert H. Lurie Children’s Hospital of Chicago.