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Single Cell Genomics of Psoriatic Skin

University of California San Francisco (UCSF) logo

University of California San Francisco (UCSF)

Status

Completed

Conditions

Psoriasis

Treatments

Procedure: Blood draw
Procedure: Skin biopsy

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT02929745
15-17769

Details and patient eligibility

About

The purpose of this study is to understand how genetics play a role in psoriasis. Specifically, a genetic allele HLA-Cw6 is known to be associated with psoriasis, and this study aims to find out how it affects genetic and protein expression in patients with psoriasis, compared to healthy people, at a single-cell level using a novel flow cytometry and RNA-sequencing protocol.

Enrollment

16 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

For subjects in the psoriasis group:

  1. Ability to provide written consent and comply with the protocol
  2. At least 18 years of age
  3. Diagnosis of plaque psoriasis for at least 6 months prior to enrollment
  4. BSA > 5% and at least one target plaque on trunk or extremities greater than 10cm2

For control subjects:

  1. Ability to provide written consent and comply with the protocol
  2. At least 18 years of age
  3. No previous diagnosis of psoriasis or other inflammatory skin conditions

Exclusion criteria

For subjects in the psoriasis group:

  1. Subject has non-plaque form of psoriasis.
  2. Subject has drug-induced psoriasis.
  3. Pregnancy at any point during the study period.
  4. Known allergy to lidocaine, other local anesthetics, or any component of local anesthetic agents.
  5. Known HIV positive status.
  6. Evidence of abnormality of any immune cell population from a drug-induced or genetic cause.
  7. Known coagulopathy.

For control subjects:

  1. Any physical examination findings by the investigators consistent with psoriasis or other inflammatory skin conditions.
  2. Pregnancy at any point during the study period.
  3. Known allergy to lidocaine, other local anesthetics, or any component of local anesthetic agents.
  4. Known HIV positive status.
  5. Evidence of abnormality of any immune cell population from a drug-induced or genetic cause.
  6. Known coagulopathy.
  7. Use of any immunosuppressant or immunomodulating therapies within 6 months.

Trial design

Primary purpose

Basic Science

Allocation

Non-Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

16 participants in 3 patient groups

10 HLA-Cw6+
Experimental group
Description:
HLA-Cw6+ patients will donate blood and skin samples
Treatment:
Procedure: Blood draw
Procedure: Skin biopsy
10 HLA Cw6-
Experimental group
Description:
HLA-Cw6- patients will donate blood and skin samples
Treatment:
Procedure: Blood draw
Procedure: Skin biopsy
Healthy Skin
Experimental group
Description:
Healthy patients will donate blood and skin samples
Treatment:
Procedure: Blood draw
Procedure: Skin biopsy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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