Atopic Dermatitis Clinical Trials

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The Real-world Treatment Patterns and Clinical Outcomes in Moderate-to-severe Atopic Dermatitis (AD) Patients Receiving Abrocitinib

Status: Recruiting
Location: See all (8) locations...
Study Type: Observational
SUMMARY

This study is to describe the real-world treatment patterns and clinical outcomes in moderate-to-severe AD patients receiving abrocitinib over a 12-month observation period, and to describe patient demographic and baseline characteristics.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 12
Healthy Volunteers: f
View:

⁃ Patients must meet all of the following inclusion criteria to be eligible for inclusion in the study:

• Patients aged ≥12 years

• Patients with confirmed diagnosis of moderate-to-severe AD as assessed by the physician

• Patients for whom the physician's decision has been made to newly prescribe abrocitinib in usual clinical practice conditions

• Evidence of a personally signed and dated informed consent/assent document indicating that the patient (or a legally acceptable representative) has been informed of all pertinent aspects of the study

Locations
Other Locations
Taiwan
Chang Gung Memorial Hospital at Kaohsiung
RECRUITING
Kaohsiung City
Kaohsiung Medical University Hospital
NOT_YET_RECRUITING
Kaohsiung City
Taipei Medical University - Shuang Ho Hospital
NOT_YET_RECRUITING
New Taipei City
MacKay Memorial Hospital
NOT_YET_RECRUITING
Taipei
NTUH
RECRUITING
Taipei
Taipei Veterans General Hospital
NOT_YET_RECRUITING
Taipei
Tri-Service General Hospital
NOT_YET_RECRUITING
Taipei
Chang Gung Hospital Linkou
NOT_YET_RECRUITING
Taoyuan District
Contact Information
Primary
Pfizer CT.gov Call Center
ClinicalTrials.gov_Inquiries@pfizer.com
1-800-718-1021
Time Frame
Start Date: 2024-07-01
Estimated Completion Date: 2026-05-15
Participants
Target number of participants: 200
Related Therapeutic Areas
Sponsors
Leads: Pfizer

This content was sourced from clinicaltrials.gov