Post-Marketing Surveillance Study of OTEZLA

NCT03284879 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1086

Last updated 2025-09-08

No results posted yet for this study

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

Sponsors & Collaborators

Principal Investigators

  • MD · Amgen

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-09-05
Primary Completion
2021-10-31
Completion
2022-03-20

Countries

  • Japan

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03284879 on ClinicalTrials.gov