UCSF Psoriasis and Skin Treatment Center
San Francisco, California, 94118, United States
NCT Number: NCT02592018
This is a single-arm, open-label study, which will examine the effect of secukinumab on the immunologic and genetic environment within psoriatic lesions.
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Notify Me18 year and older
All sexes
Interventional
Phase 4
San Francisco, California, 94118, United States
Quantitative analysis of the immunologic changes in immune cell populations will be performed after secukinumab treatment in 15 patients at weeks 2, 4, and 12 compared to baseline week 0. The immunologic profiles in psoriasis patients will also be compared to healthy control skin surgical discard specimens (n=10). The number of differentially expressed genes in each cell population will be quantified by RNA-seq at weeks 2, 4, 12 after secukinumab compared to baseline.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Secukinumab 300mg SQ at weeks 0, 1, 2, 3, 4, and every 4 weeks thereafter until week 48. Skin biopsy procedures will be performed at weeks 0, 2, 4, and 12.
Other names: Cosentyx
Time frame: Baseline to Week 2
Time frame: Baseline to Week 4
Time frame: Baseline to Week 12
Time frame: Baseline to Week 2
by RNA-seq
Time frame: Baseline to Week 4
by RNA-seq
Time frame: Baseline to Week 12
by RNA-seq
Time frame: Baseline to Week 2
by RNA-seq
Time frame: Baseline to Week 4
by RNA-seq
Time frame: Baseline to Week 12
by RNA-seq
Time frame: Baseline to Week 2
by RNA-seq
Time frame: Baseline to Week 4
by RNA-seq
Time frame: Baseline to Week 12
by RNA-seq
University of California, San Francisco
Other
Characterization of the Response to Secukinumab in Plaque Psoriasis Using Novel Immunologic and Genetic Profiling
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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