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Trials / Completed

CompletedNCT03284879

Post-Marketing Surveillance Study of OTEZLA

OTEZLA® Tablets Drug Use-Results Survey

Status
Completed
Phase
Study type
Observational
Enrollment
1,086 (actual)
Sponsor
Amgen · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

To evaluate the safety and efficacy of OTEZLA in actual clinical settings of use in patients with Psoriasis vulgaris that is with an inadequate response to topical therapies and Psoriasis arthropathica 1. Planned registration period 2 years 2. Planned surveillance period for 4 years from 6 months after launch

Conditions

Timeline

Start date
2017-09-05
Primary completion
2021-10-31
Completion
2022-03-20
First posted
2017-09-15
Last updated
2025-09-08

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT03284879. Inclusion in this directory is not an endorsement.

Post-Marketing Surveillance Study of OTEZLA (NCT03284879) · Clinical Trials Directory