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ABSTRACT: Introduction
The benefit/risk profiles of biologics can be affected by comorbidities, certain demographic characteristics, and concomitant medications; therefore, it is important to evaluate the long-term safety profiles of biologics across broad patient populations. Guselkumab was well tolerated and efficacious across individual pivotal clinical studies in adults with moderate-to-severe psoriasis and/or active psoriatic arthritis (PsA).Objectives
The objective of the current analysis was to evaluate guselkumab safety in a large population of patients with psoriatic disease by pooling adverse event (AE) data from 11 phase II/III studies (seven in psoriasis; four in PsA).Methods
Guselkumab was generally administered as 100 mg subcutaneous injections at Week 0, Week 4
SUBMITTER: Strober B
PROVIDER: S-EPMC10764399 | biostudies-literature | 2024 Jan
REPOSITORIES: biostudies-literature