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Janssen's Tremfya (guselkumab) Receives FDA's Approval for Moderate-to-Severe Plaque Psoriasis in Adults

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Janssen's Tremfya (guselkumab) Receives FDA's Approval for Moderate-to-Severe Plaque Psoriasis in Adults

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  • The approval is based on P-III study results assessing Tremfya (guselkumab- 100mg) vs PBO in 78 patients with moderate-to-severe plaque psoriasis
  • P-III ORION study: IGA score of 0/1 or PASI 90 @16wks. (81%- 76% vs 0%-0%); IGA score of 0 @16 wk (56% vs 0%); PASI 100 response @16 wks (50% vs 0%)
  • Tremfya (guselkumab-100mg- SC) is a mAb offering one-press patient-controlled injector inhibiting interleukin (IL)-23- evaluated in two P-III trials for active psoriatic arthritis & Crohn’s disease and is approved in the US- EU- Canada & Japan for moderate-to-severe plaque psoriasis in adults

Ref: Janssen | Image: Janssen

Click here to­ read the full press release 

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