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OpenTrials
Completed

NCT Number: NCT02592018

Immunologic Response to Secukinumab in Plaque Psoriasis

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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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

UCSF Psoriasis and Skin Treatment Center

San Francisco, California, 94118, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Ability to provide written informed consent and comply with the protocol.
  • At least 18 years of age.
  • Diagnosis of predominately plaque psoriasis for at least 6 months prior to enrollment.
  • Subject is considered a candidate for phototherapy or systemic therapy
  • PASI ≥ 12
  • PGA ≥ 3
  • Subject has a negative Quantiferon Gold, or if positive undergoes CXR. If CXR negative, subject initiated prophylactic therapy with isoniazid for a course of 9 months with one month of therapy completed prior to first dose of secukinumab.
  • Subject is unlikely to conceive (male, post-menopausal, or using adequate oral contraceptive therapy or IUD).
  • Physical exam within clinically acceptable limits.

Exclusion criteria

  • Subject is unable to provide written informed consent or comply with the protocol.
  • Subject is younger than 18 years of age.
  • Subject has predominately non-plaque form of psoriasis.
  • Subject with mild psoriasis (PASI<12 and PGA<3) or is not a candidate for phototherapy or systemic treatments.
  • Subject has drug-induced psoriasis.
  • Subject with current, or a history of, severe psoriatic arthritis well controlled on current therapy.
  • Subjects with a serum creatinine level exceeding 176.8 μmol/L (2.0 mg/dl).
  • Screening total white blood cell (WBC count) < 2,500/μl, platelets < 100,000/μl, neutrophils < 1,500/μl, or hemoglobin <8.5 g/dl.
  • Evidence of active tuberculosis infection as defined by a positive QuantiFERON TB-Gold test (QFT) with a positive chest X-ray at screening, or untreated latent tuberculosis defined by positive QFT with a negative chest X-ray without prophylactic therapy with isoniazid for a course of 9 months with one month of therapy completed prior to first dose of secukinumab.
  • History of an ongoing, chronic or recurrent infectious disease including past medical history record of HIV, hepatitis B or hepatitis C.
  • Subjects possess other diagnoses that, in the investigator's opinion, preclude him/her from safely participating in this study or interfere with the evaluation of the subject's psoriasis.
  • History of known or suspected intolerance to any of the ingredients of the investigational study product.

Treatment and study plan

secukinumab

Drug

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

Primary outcomes

  1. Change in Percentage of CD4+ T Effector Cells Expressing IL17 Compared to Baseline

    Time frame: Baseline to Week 2

  2. Change in Percentage of CD4+ T Effector Cells Expressing IL17 Compared to Baseline

    Time frame: Baseline to Week 4

  3. Change in Percentage of CD4+ T Effector Cells Expressing IL17 Compared to Baseline

    Time frame: Baseline to Week 12

Secondary outcomes

  1. Change in Number of Differentially Expressed Genes in CD4+ Effectors Compared to Baseline Across All Participants

    Time frame: Baseline to Week 2

    by RNA-seq

  2. Change in Number of Differentially Expressed Genes in CD4+ Effectors Compared to Baseline

    Time frame: Baseline to Week 4

    by RNA-seq

  3. Change in Number of Differentially Expressed Genes in CD4+ Effectors Compared to Baseline

    Time frame: Baseline to Week 12

    by RNA-seq

  4. Change in Number of Differentially Expressed Genes in CD4+ T Regs Compared to Baseline

    Time frame: Baseline to Week 2

    by RNA-seq

  5. Change in Number of Differentially Expressed Genes in CD4+ T Regs Compared to Baseline

    Time frame: Baseline to Week 4

    by RNA-seq

  6. Change in Number of Differentially Expressed Genes in CD4+ T Regs Compared to Baseline

    Time frame: Baseline to Week 12

    by RNA-seq

  7. Change in Number of Differentially Expressed Genes in CD8+ T Effectors Compared to Baseline

    Time frame: Baseline to Week 2

    by RNA-seq

  8. Change in Number of Differentially Expressed Genes in CD8+ T Effectors Compared to Baseline

    Time frame: Baseline to Week 4

    by RNA-seq

  9. Change in Number of Differentially Expressed Genes in CD8+ T Effectors Compared to Baseline

    Time frame: Baseline to Week 12

    by RNA-seq

Sponsors and collaborators

Lead sponsor

University of California, San Francisco

Other

Collaborators

  • Novartis Pharmaceuticals

Registry information

Official study title

Characterization of the Response to Secukinumab in Plaque Psoriasis Using Novel Immunologic and Genetic Profiling

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Oct 30, 2015
Registry last updated
Sep 16, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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