FDA Approves Ixifi® (infliximab-qbtx), Third Biosimilar of Remicade® in U.S.

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The FDA announced that it has approved Pfizer’s Ixifi® (infliximab-qbtx) as a biosimilar to Remicade®. Ixifi® is indicated for the treatment of most of the same conditions as its reference product: Crohn’s disease, pediatric Crohn’s disease, ulcerative colitis (in adult patients), rheumatoid arthritis, ankylosing spondylitis and plaque psoriasis.  (Remicade® is additionally indicated for the treatment of pediatric ulcerative colitis.)

Ixifi® is the ninth biosimilar overall to obtain FDA approval under the abbreviated regulatory pathway of the BPCIA.  It is the third FDA-approved biosimilar of Remicade® to receive FDA approval, after Celltrion’s Inflectra® (infliximab-dyyb) in April 2016 and Samsung Bioepis’s Renflexis® (infliximab-abda) in April of this year.

Stay tuned to Big Molecule Watch for further developments.

DISCLAIMER: Because of the generality of this update, the information provided herein may not be applicable in all situations and should not be acted upon without specific legal advice based on particular situations.

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