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Janssen's IL-12/IL-23 inhibitor submits a new application to the FDA for the treatment of psoriatic arthritis in children

 Last Update: 2021-12-11
 Source: Internet
 Author: User

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Recently, Janssen, a subsidiary of Johnson & Johnson, announced that it has submitted its IL-12/IL-23 inhibitor Stelara (ustekinumab) supplementary biologics license application (sBLA) to the US FDA for the treatment of 5 Children with juvenile psoriatic arthritis (jPsA) over the age of years

Stelara is a humanized IL-12 and IL-23 antibody.

This application was supported by nine trials for adults with active psoriatic arthritis, adults and children with moderate to severe plaque psoriasis

Reference materials:

[1] Janssen Submits Application Seeking US FDA Approval of Stelara® (ustekinumab) for the Treatment of Pediatric Patients With Juvenile Psoriatic Arthritis.

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Express Janssen IL-12/IL-23 inhibitor submits a new application to the FDA for the treatment of children with psoriatic arthritis

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Janssen's IL-12/IL-23 inhibitor submits a new application to the FDA for the treatment of psoriatic arthritis in children

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Express Janssen IL-12/IL-23 inhibitor submits a new application to the FDA for the treatment of children with psoriatic arthritis