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NCT06937060: SEMPSO
Effect of Semaglutide in Patients With Psoriasis and Obesity
Phase 3 trial testing semaglutide in Psoriasis (PsO) in 14 participants. Currently enrolling.
31 July 2026
Quick facts
| Lead sponsor | The University of Hong Kong |
|---|---|
| Phase | Phase 3 |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 14 |
| Start date | 20 March 2025 |
| Primary completion | 31 July 2026 |
| Estimated completion | 31 January 2027 |
| Sites | 1 location across Hong Kong |
Drugs / interventions tested
- semaglutide (semaglutide) — full drug profile →
Conditions studied
- Psoriasis (PsO) — all drugs for Psoriasis (PsO) →
- Obesity and Overweight — all drugs for Obesity and Overweight →
Sponsor
The University of Hong Kong
Who can join
Adults 18 to 75, any sex, with Psoriasis (PsO) or Obesity and Overweight. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
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.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Glucagon-like peptide-1 receptor agonists in psoriasis and psoriatic arthritis: emerging evidence and future research opportunities.
Ciancio G, Maranini B, Sandri G, Amati G, et al · · 2026 · PMID 42131335 · DOI 10.3389/fimmu.2026.1744308
Verify or expand the search:
- PubMed search for NCT06937060
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other recruiting trials for Psoriasis (PsO)
Currently open trials in the same condition.
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- NCT07233291 — A Pilot Study to Assess How Safe and Effective Oral Roflumilast is for Treating Moderate to Severe Psoriasis in Adults · Phase 2 · recruiting
- NCT07169019 — Microbiome and Clinical Response to Probiotics and Methotrexate in Early Psoriasis: a Pilot Study · EARLY_PHASE1 · recruiting
Other The University of Hong Kong trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06937060 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by The University of Hong Kong
- Last refreshed: 13 May 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06937060.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing