Johnson & Johnson will launch its first-in-class interleukin-23 inhibitor Tremfya (guselkumab) at a premium price that is nonetheless competitive with other new biologic entrants for moderate-to-sever plaque psoriasis. The company announced the FDA approval of Tremfya July 13, with plans to launch the drug within two weeks.
J&J's First-In-Class Tremfya Poised To Join A Crowded Psoriasis Market
FDA approved Johnson & Johnson's IL-23 blocker guselkumab July 13; the drug will be priced at an annual wholesale acquisition cost of $58,100, roughly in line with the currently marketed IL-17 blocker Cosentyx.

More from New Products
Strong sales growth for the German group’s SGLT2 inhibitor in 2024
Pipeline Watch is a weekly snapshot of selected late-stage clinical trial events and approvals announced by pharmaceutical and biotech companies at medical and industry conferences, in financial and company presentations, and in company releases and statements.
The small interference RNA therapeutic can be used by patients regardless of inhibitor status.
The company is planning to launch oxylanthanum carbonate for chronic kidney disease patients on dialysis with hyperphosphatemia.
More from Scrip
CEO Kris Elverum told Scrip about the start-up’s platform for editing RNA to correct genetic variants that cause harm and to reproduce healthy variants as a means of treating disease.
The study’s failure in the overall MDD population was not a surprise, but solriamfetol’s efficacy in MDD with EDS provided a rationale for testing it in that subpopulation.
Pharma executives and investors are waiting with bated breath to find out if President Trump will include drugs in a new round of tariffs to be announced on 2 April.