Overview
The objective of this Study is to confirm the safety during the long-term use of this drug and the effectiveness during the use of this drug under the actual use in the patients treated with this drug.
Description
This study is an open-label, multi-center, one arm prospective observational cohort study of patients receiving this drug. The investigators complete the CRF based on the information extracted from the medical record created in daily medical practice.
Eligibility
Inclusion Criteria:
Patients must meet all of the following inclusion criteria to be eligible for inclusion in
the study:
- Patients with alopecia areata who start receiving this drug for the first time after
the contract date of this study
- Patients who have not participated in a clinical trial (clinical study) of this drug
Exclusion Criteria:
Patients meeting any of the following criteria will not be included in the study:
- Patients previously enrolled in this study
- Patients with a history of treatment with this drug (including investigational
product)