Registry of Psoriasis Health Outcomes: A Longitudinal Real-world Collaboration (RePhlect) - A Real-World, Prospective, Observational Study of the Comparative Effectiveness of Deucravacitinib in Adults With Plaque Psoriasis in Japan

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug
Study Type: Observational
SUMMARY

This is a prospective, observational, real-world study of adult participants in Japan with physician-reported diagnosis of plaque psoriasis treated with deucravacitinib or apremilast.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Japanese adult participants aged 18 years old or older

• Physician-reported diagnosis of plaque psoriasis

• Newly initiating deucravacitinib or apremilast according to the label

• Participants who have signed informed consent

Locations
Other Locations
Japan
Fukuoka University Hospital
RECRUITING
Fukuoka
Mebix. Inc.
RECRUITING
Minato-ku
Contact Information
Primary
BMS Study Connect Contact Center www.BMSStudyConnect.com
Clinical.Trials@bms.com
855-907-3286
Backup
First line of the email MUST contain NCT # and Site #.
Time Frame
Start Date: 2024-01-22
Estimated Completion Date: 2029-12-31
Participants
Target number of participants: 600
Treatments
Participants that have initiated deucravacitinib treatment
Participants that have initiated apremilast treatment
Related Therapeutic Areas
Sponsors
Leads: Bristol-Myers Squibb

This content was sourced from clinicaltrials.gov