Actively Recruiting
Effect of Semaglutide in Patients With Psoriasis and Obesity
Led by The University of Hong Kong · Updated on 2025-05-13
14
Participants Needed
1
Research Sites
97 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Obesity is well known to be an important comorbidity of psoriasis. It gives rise to higher risk of psoriatic arthritis, more severe disease and also poorer response to biologics. Weight loss can lead to reduction in psoriasis severity. Previous studies had demonstrated the efficacy of older glucagon-like peptide-1 receptor agonist (GLP1 RA) on improvement of psoriatic disease activity. Effective weight loss has been achieved by newer GLP1 RA.7 It is also known to reduce cardiovascular outcomes in patient without diabetes. Trials on the effect of semaglutide on psoriasis has not been performed except case reports. Semaglutide is an injectable prescription medicine that may help adults and children aged 12 years and older with obesity or some adults with excess weight (overweight) who also have weight-related medical problem to help them lose weight. It contains a GLP1 RA indicated as an adjunct to diet and exercise to improve glycemic control. It has potential anti-inflammatory effects on top of weight reduction, that may lead to improvement in psoriatic disease activity. This is an open-label, single-armed, prospective pilot trial on obese, psoriasis patients. The investigators aim to recruit 14 patients. Patients will be maintained on standard care for their psoriasis. Add-on treatment with semaglutide of up to 2.0mg per week will be administered to the intervention arm in addition to lifestyle intervention. Treatment with previous systemic immunosuppressants is allowed. The maximum study duration for a single subject in the study will be approximately 36 weeks, 4 weeks of screening, 24-week treatment period, and a 12-week safety follow up period after the last study dose of semaglutide at week 24.
CONDITIONS
Official Title
Effect of Semaglutide in Patients With Psoriasis and Obesity
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Clinical diagnosis of psoriatic disease for at least 6 months before consent
- Female participants who are sexually active and not postmenopausal must agree to remain abstinent or use two effective contraception methods
- Age between 18 and 75 years
- Adults with BMI of 30 kg/m2 or greater, or BMI of 27 kg/m2 or greater with at least one weight-related comorbidity such as hypertension, type 2 diabetes mellitus, or dyslipidemia
- Moderate to severe psoriasis with a PASI score of 5 or higher
- Chinese ethnicity
- On a stable dose of standard psoriasis treatment
- Ability to comply with study requirements
You will not qualify if you...
- Refusal to give consent
- Contraindication to GLP1 receptor agonist use
- History of pancreatitis
- History of multiple endocrine neoplasia (MEN) or medullary thyroid carcinoma (MTC)
- Known allergy to semaglutide or its ingredients
- Type 1 diabetes
- Gallbladder disease
- Active malignancy or history of cancer within the past 5 years
- Active infection requiring systemic treatment within 4 weeks before baseline
- Pregnancy or breastfeeding
- History of allergic reaction related to the investigational product
- Major psychiatric illness
- Treatment with live or attenuated vaccine within 28 days before randomization
- History of alcohol or substance abuse within 6 months before screening
- History of suicide attempts or active suicidal thoughts
AI-Screening
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Trial Site Locations
Total: 1 location
1
The University of Hong Kong, Department of Medicine
Hong Kong, Hong Kong
Actively Recruiting
Research Team
M
Man Ho Martin Chung
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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