With FDA nod for Tremfya, J&J moves quickly to shore up psoriasis portfolio

14 July 2017

After cashing in a priority review voucher with the US Food and Drug Administration, healthcare giant Johnson & Johnson's (NYSE: JNJ) biopharmaceutical arm Janssen Biotech has been given approval to market Tremfya (guselkumab) as a treatment for moderate to severe plaque psoriasis.

J&J’s interleukin blocker targets interleukin (IL)-23, in contrast to rival next-gen psoriasis treatments Taltz (ixekizumab) and Cosentyx (secukinumab), which target IL-17.

The indication is already hotly contested, with Valeant Pharmaceuticals' (TSX: VRX) affordably-priced IL-17 blocker Siliq (brodalumab) adding to those therapeutic options from Novartis (NOVN: VX) and Eli Lilly (NYSE: LLY).

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