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A Study of the Comparative Effectiveness of Deucravacitinib in Adults With Plaque Psoriasis in Japan (RePhlect)

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NCT06382987 · readout in 1,230 d

Sponsored by Bristol-Myers Squibb (industry) · BMY — their whole pipeline →.

Phase
Status
Recruiting
Study type
Observational
Enrollment
600estimated
Sites
2
Country
Japan

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-01-22actualWhen the study began enrolling
Primary completion2029-12-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2029-12-31estimatedThe whole study's end, after follow-up
First posted2024-04-25actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2024-04-25actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Plaque Psoriasis

Interventions

  • Drug: Deucravacitinib
  • Drug: Apremilast

Primary outcomes

what the primary-completion date above is the date OF
Change in percent Body Surface Area (BSA) involved affected by plaque psoriasis from baseline to follow up in participants treated with deucravacitinib.
measured 1 month, 3 months, 6 months and every 6 months up to 5 years
Number of participants who achieved Physician's Global Assessment (PGA) of 0/1 from baseline to follow-up
measured 1 month, 3 months, 6 months and every 6 months up to 5 years
Number of participants who achieved Absolute Psoriasis Area and Severity Index (aPASI) of ≤2 from baseline to follow-up
measured 1 month, 3 months, 6 months and every 6 months up to 5 years
Number of participants who achieved Dermatology Life Quality Index (DLQI) of 0 /1 from baseline to follow-up
measured 1 month, 3 months, 6 months and every 6 months up to 5 years
Participant duration of treatment (time difference between date of treatment initiation to date of discontinuation)
measured 1 month, 3 months, 6 months and every 6 months up to 5 years

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