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Retrospective observational study of patients with atopic dermatitis in remission with Upadacitinib.

Retrospective Observational Study of Atopic Dermatitis Patient After Achieving Remission by Upadacitinib in Japanese Real-world Practice - ROADMAP study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000054106
Enrollment
300
Registered
2024-04-12
Start date
2024-04-20
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atopic Dermatitis

Interventions

None listed

Sponsors

Non-Profit Organization Health Institute Research of Skin
Lead Sponsor
Abbvie LLC.
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) AD patients receiving upadacitinib for the treatment of AD 2) Patients aged 12 years or older at the start of treatment with Upadacitinib 3) Patients who achieved remission after treatment with Upadacitinib 4) Patients who can be followed up for at least 1 year after remission

Exclusion criteria

Exclusion criteria: 1) Cases of use clearly off-label for Upadacitinib 2) Patients who have requested to refuse to participate in the study

Design outcomes

Primary

MeasureTime frame
Remission maintenance rate at 1 year after achieving remission with Upadacitinib

Secondary

MeasureTime frame
Upadacitinib for atopic dermatitis: the actual treatment of atopic dermatitis.

Countries

Japan

Contacts

Public ContactRYOICHI TAGUCHI

EBC&M LLC Clinical Division

ryoichi_taguchi@ebc-m.com0364353833

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026