Reduced Vaccine Response to HZ/su in SLE
Recruiting now
Conditions studied: Vaccine Reaction, Zoster, Systemic Lupus Erythematosus
In brief
The goal of this observational study is to compare the vaccine response to the 2 doses of the adjuvanted herpes zoster subunit vaccine(HZ/su, "Shingrix") in patients with SLE and the age-, sex-, ethnicity-matched controls without autoimmune disease.
Key facts
- Study ID
- NCT07636044
- Run by
- Seoul National University Hospital
- People needed
- 80
- Starts
- 2024-10-01
- Expected to finish
- 2030-10-01
- Last updated by the study team
- 2026-06-09
Who can join
Age: 50 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Males or females ≥ 50 years of age at time of consent
- ≥ 4 of the 1997 ACR13 or the 2012 SLICC/ACR criteria for SLE (14, 15)
- Clinically stable SLE
- Stable dose of one or more of the following immunosuppressive treatment ≥ 4 weeks
- Corticosteroid use: ≥ 5mg/day of prednisolone equivalent
- Antimalarials (≤ 400 mg/day)
- Azathioprine (≤ 3 mg/kg/day)
- Mycophenolate mofetil (≤ 3 mg/day)
- Tacrolimus (≤ 5mg/day)
- Methotrexate (≤ 20mg/week)
- Cyclosphosphamide (≤ 1mg/BSA/month)
- Must be eligible for the indication of adjuvanted herpes zoster subunit vaccine
- Must understand and voluntarily sign an informed consent form including writing consent for data protection
You may not qualify if…
- Pregnant or lactating females
- Acute infection with temperature >38C at the time of vaccination
- Previous anaphylactic response to vaccine components or to egg
- History of Guillain-Barre syndrome or demyelinating syndromes
- Any condition including laboratory abnormality which places the subject at unacceptable risk
- Subjects who decline to participate
Where it is running
- Seoul National University Hospital — Seoul, South Korea (enrolling)
Full record on ClinicalTrials.gov
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