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GLP-1 Receptors in Normal Skin and Skin From Patients With Psoriasis

U

University Hospital, Gentofte, Copenhagen

Status

Unknown

Conditions

Reduction of Psoriasis Following Liraglutide Therapy in Terms of PASI and DLQI

Treatments

Drug: Liraglutide
Drug: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT01451905
GLP1-PSO

Details and patient eligibility

About

To examine GLP-1 receptors in skin of psoriasis patients compared with the skin of humans with no skin disease

Enrollment

12 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

4.3 Inclusion Criteria

  • Caucasians above 18 years of age
  • Plaque psoriasis
  • PASI score >10
  • No treatment or stable treatment of psoriasis during at least 3 months before inclusion
  • Steady weight through 3 months with a body mass index (BMI) above 27 kg/m2
  • Normal blood pressure
  • Spiral or hormonal birth control for fertile women during the entire treatment period and at least 3 days after the end of the treatment period (~5 times the plasma half-life) 4.4 Exclusion Criteria
  • Psoriasis arthritis
  • Fasting plasma glucose > 7.5 mmol/L or HbA1c > 7.5%
  • Type 1 diabetes
  • Treatment for type 2 diabetes with GLP-1-based medicine (DDP-4-inhibitors or GLP-1-receptor-agonists)
  • Heart failure, NYHA class III-IV
  • Uraemia, end-stage renal disease, or any other cause of impaired renal function with s-creatinine >150 µM and/or albuminuria
  • Liver disease (alanine amino transferase (ALAT) and/or aspartate amino transferase (ASAT) >2 x upper normal serum levels)
  • Anaemia
  • Acute or chronic pancreatitis
  • Struma or thyroid cancer
  • Pregnancy or breast feeding
  • Inability to complete the study

Trial design

12 participants in 2 patient groups, including a placebo group

Psoriasis
Active Comparator group
Treatment:
Drug: Liraglutide
Placebo
Placebo Comparator group
Treatment:
Drug: Placebo

Trial contacts and locations

1

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Central trial contact

Annesofie Faurschou, MD PhD

Data sourced from clinicaltrials.gov

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