Sarpatwari A, Barenie RE, Curfman GD, Darrow JJ, Kesselheim AS - Clinical Pharmacology & Therapeutics
The US biosimilar market has experienced limited growth since the 2010 creation of an abbreviated approval pathway, with only 13 FDA approvals and 6 products actually available to patients as of November 2018, due to manufacturing, regulatory, and marketing barriers. The authors recommend reforms to address these obstacles and accelerate biosimilar market entry and adoption.
VIEW SOURCE
Eisenkraft Klein D, Kesselheim AS - Clinical Pharmacology & Therapeutics
Daval CJR, Kesselheim AS - STAT
Cai CL, Bucha S, Kesselheim AS, Rome BN - Journal of General Internal Medicine