9 out of 10

active PsA patients continued therapy on TREMFYA® in DISCOVER 2 through 2 years (Week 100) and in DISCOVER 1 prior to Week 481*

DISCOVER 2: Study disposition at Week 24 and through Week 100

DISCOVER 2 Adverse events chart between week 24 and week 100
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DISCOVER 2 Adverse events chart between week 24 and week 100

DISCOVER 1: Study disposition at Week 24 and prior to Week 48

DISCOVER 1 adverse events chart between week 24 and week 48
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DISCOVER 1 adverse events chart between week 24 and week 48

No conclusions regarding clinical efficacy or safety can be drawn.

*Year 2 represents Week 100.

Discontinuations shown for patients who were randomized and received at least 1 study drug administration.

248 patients in DISCOVER 2 were randomized to the TREMFYA® 100 mg q4w dosing regimen through Week 112; TREMFYA® q4w was not an FDA-approved dosing regimen.

§1 patient-initiated, protocol-prohibited medication in the placebo group through Week 24.

Reference: 1. Data on file. Janssen Biotech, Inc.

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