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NOT YET RECRUITING
NCT06863493
PHASE2/PHASE3

Comparison of Otezla to SFA-002 to Placebo in Plaque Psoriasis Patients

Sponsor: SFA Therapeutics

View on ClinicalTrials.gov

Summary

The goal of this clinical trial\] is to learn if SFA002 can treat mild, moderate and severe plaque psoriasis as good or better than Otezla, compared to placebo in adult and pediatric patients. The main questions it aims to answer are: How much does oral SFA002 treatment improve plaque psoriasis measured at different timepoints, 12 weeks, 24 weeks and 52 weeks of treatment. How much does Oral Otezla (Apremilast) improve plaque psoriasis measured at different timepoints, 12 weeks, 24 weeks and 52 weeks of treatment. These treatments will be compared to placebo, a look-alike substance that contains no drug. Participants will be randomly placed into 3 groups to receive either SFA002, or oral apremilast or placebo for the duration of the trial. Patients that do not respond to apremilast or placebo treatment in 12 weeks will be offered the opportunity to take SFA002 for the remainder of the study. There may be a higher burden for participants in this study compared to usual standard of care. Participants will attend regular visits per routine clinical practice. The effect of the treatment will be checked by medical assessments, checking for side effects, and questionnaires.

Official title: Study of the Safety and Effectiveness of Oral SFA-002 Compared to Oral Apremilast (Otezla) Tablets and Placebo in Mild to Severe Plaque Psoriasis

Key Details

Gender

All

Age Range

18 Years - 85 Years

Study Type

INTERVENTIONAL

Enrollment

125

Start Date

2025-06-01

Completion Date

2026-09-01

Last Updated

2025-03-11

Healthy Volunteers

No

Conditions

Interventions

DRUG

SFA002

SFA002 760mg

DRUG

Otezla

Oral Otezla 30mg

DRUG

Placebo

Placebo will be matched to whichever drug is assigned when randomized