FDA approves lower-cost alternative to biotech drug Humira
WASHINGTON (AP) — Federal regulators have approved the first alternative version of the second-biggest selling drug in the world, AbbVie’s Humira, a blockbuster injection used to treat rheumatoid arthritis and other inflammatory diseases.
The Food and Drug Administration cleared the near-copy of the drug, dubbed Amjevita, developed by Amgen Inc. of Thousand Oaks, California. Regulators approved the drug for more than a half-dozen conditions listed on the original drug’s label, including severe psoriasis and Crohn’s disease.
Humira posted sales of nearly $15 billion last year and was for many years the top-selling prescription drug in the world, according to data from IMS Health.
AbbVie Inc. is based in North Chicago, Illinois.