New survey: When will FDA approve first biosimilar/biogeneric?
Definitions for this survey:
• A biosimilar is a non-substitutable biologic reviewed under a 351(k) submission whose approval for marketing is based, in part, on the safety and efficacy of a “reference” drug that was previously approved under a BLA.
• A biogeneric is a substitutable biologic reviewed under a 351(k) submission whose approval is based, in part, on the safety and efficacy of a “reference” drug that was previously approved under a BLA. A biogeneric may be substituted for the reference drug by a pharmacist or hospital formulary without explicit permission from the prescribing MD.
(Please see #msg-48581353 for provisions of the 2010 law that empowers the FDA to approve biosimilars and biogenerics. Note: Lovenox and Copaxone are not biosimilars or biogenerics, but rather complex mixtures regulated by the FDA as small-molecule drugs.)
Q1: When will FDA approve the first biosimilar? a) 2012 b) 2013 c) 2014 d) 2015 e) 2016 or later
Q2: When will FDA approve the first biogeneric? a) 2012 b) 2013 c) 2014 d) 2015 e) 2016 or later