atopic dermatitis
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients treated with tralokinumab for the treatment of AD which is inadequately responsive to conventional therapies Patients with medical records of at least 16 weeks or more after starting tralokinumab treatment
Exclusion criteria
Exclusion criteria: Cases where tralokinumab was clearly used outside its approved indications. Patients with prior experience participating in clinical trials for tralokinumab. Patients who have refused to participate in this study (i.e., refused the use of their medical records). The opportunity for research subjects to refuse the use of their medical records in this study (opt-out) will be ensured.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Distribution of IGA scores from the start of Tralokinumab administration at16 weeks | — |
Countries
Japan
Contacts
EBC&M LLC Clinical Division