The National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) supports a range of clinical trials studying new and existing interventions for prevention and treatment of arthritis, musculoskeletal, and skin diseases. Recruitment for this clinical trial complete. Updates will be made to this page when the study completes data analysis and results become available. Please check back often and find out how these studies have contributed to generating new knowledge about diseases and conditions within the NIAMS mission area.
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Herpes zoster (HZ), also known as "shingles", is caused by reactivation and multiplication of the ubiquitous varicella zoster virus (VZV) that remains latent in everyone's sensory neurons following varicella, or "chickenpox". Among individuals who live to age 85, the lifetime risk for HZ is 50%, and more than one in five individuals affected by zoster develop post-herpetic neuralgia, resulting in chronic pain. Other serious complications include encephalitis, permanent vision loss, or more rarely, dissemination and death. Fortunately, a live attenuated vaccine is available and can reduce HZ risk by up to 70%. For patients with rheumatoid arthritis (RA), this vaccine has great potential to provide improved quality of life by reducing the incidence and complications associated with zoster. Due to the underlying disease and/or treatments (e.g. steroids) for rheumatoid arthritis (RA), the risk of herpes zoster in RA patients is approximately double in the general population. This increased risk should make prevention of zoster and vaccination exceedingly important for RA patients.
In light of 1) a substantial elevated HZ risk among RA patients; 2) national data showing most RA patients are not vaccinated for HZ; and 3) the high effectiveness of this vaccine in the general population, the investigators propose to conduct the Varicella zostER VaccinE (VERVE) trial, a randomized, double-blind, placebo-controlled study to evaluate the safety, tolerability, and long-term effectiveness of the live herpes zoster vaccine. Additionally, the investigators will study vaccine tolerability and long-term effectiveness through a linkage to health plan data to allow for cost-effective follow-up while minimizing participant and study-site burden. Results from this study will facilitate the parent trial and change RA management by demonstrating the clinical safety and immunogenicity of the live zoster vaccine among current anti-TNF users. Rheumatologists and other providers will be able to improve the care, outcomes, and quality of life for patients using anti-TNF therapy, substantially decreasing the morbidity of herpes zoster and its complications over a lifetime.
Ages Eligible for Study: 50 Years and older (Adult, Older Adult)
Sexes Eligible for Study: All
Accepts Healthy Volunteers: No
- Must be 50 years of age or older
- Must be currently treated with an anti-TNF therapy** at the time of study drug administration, allowing for small deviations in dosing frequency and logistic feasibility (e.g. study visits to occur on a week day). Date of previous dose of medication is required. Specifically, meets one of the following: Etanercept dose within 9 days (1 week + 2 days), Adalimumab dose within 16 days (2 weeks + 2 days), Certolizumab Subcutaneous (SC) dose within 16 to 32 days depending on frequency schedule (2 weeks + 2 days, or 4 weeks and 4 days), Golimumab Subcutaneous (SC) dose within 32 days (4 weeks + 4 days), Golimumab Intravenous (IV) dose within 64 days (9 weeks + 1 day), Infliximab IV dose within last 64 days (9 weeks + 1 day)
**any form of biosimilar for the above listed anti-TNF medications is acceptable
- Diagnosis of RA or another inflammatory arthritis (Phase Ia); or RA, another inflammatory arthritis, or other inflammatory condition (e.g. psoriasis) requiring use of anti-TNF therapy (Phase Ib and II)
- Phase I subjects must test positive for VZV immunoglobulin G (IgG)
- Subjects should have a self-reported history of prior varicella infection (i.e. chicken pox) or long-term residence (>30 years) in the continental US.
- Phase Ia subjects must not have received any oral or systemic glucocorticoids within 30 days prior to vaccination. Intra-articular glucocorticoid injections and inhaled glucocorticoids within the previous 30 days are acceptable.
- Subjects should be on stable doses of all biologic and non-biologic DMARDs for a minimum of 30 days prior to vaccination.
- Eligible women must be post-menopausal (> 1 year since last menstrual period) or have a surgical history of bilateral oophorectomy or hysterectomy.
- Subjects should be ambulatory, community dwelling and capable of giving informed consent.
- Documented VZV negative result
- Prior use of the zoster vaccine (Zostavax®, Merck)
- Glucocorticoids at a prednisone-equivalent daily dose > 10mg/day (for Phase 1b and Phase II participants; all systemic glucocorticoid use is prohibited for Phase Ia patients)
- Any known contraindication to Zostavax® vaccine, including allergy or sensitivity to gelatin or any other vaccine component
- Known HIV/AIDS
- Currently receiving radiation or chemotherapy for any type of malignancy
- Any current use (within the last 30 days) of acyclovir, valacyclovir, famciclovir, or foscarnet
- Receipt of any other immunizations within one month before study vaccination (2 weeks in the case of inactivated influenza vaccines or other non-replicating immunization products [e.g., diphtheria-tetanus (dT), pneumococcal vaccine, hepatitis A vaccine, hepatitis B vaccine]), or scheduled within 6 weeks after recruitment.
- Active infection or inter-current illness (e.g., urinary tract infection, influenza)
- Participated in an investigational study within 1 month prior to study entry
- Active drug or alcohol use, dependence, or any other reason that, in the opinion of the site investigator, would interfere with the study
- Significant underlying illness that would be expected to prevent completion of the study (e.g., life-threatening disease likely to limit survival to less than 3 years)
- Any other reason that, in the opinion of the site investigator, would interfere with required study related evaluations (e.g. uncontrolled comorbidity, life expectancy < 1 year)
- Patients who have household contact with varicella-susceptible pregnant women or severely immunosuppressed individuals without history of primary varicella.
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Prevention
Rheumatology Associates, Birmingham, Alabama, United States, 35205
Total Skin and Beauty Dermatology Center, PC, Birmingham, Alabama, United States, 35205
University of Alabama at Birmingham, Birmingham, Alabama, United States, 35294
Rheumatology Associates of North Alabama, PC, Huntsville, Alabama, United States, 35801
Clinical and Translational Research Center of Alabama, PC, Tuscaloosa, Alabama, United States, 35406
SunValley Arthritis Center, Ltd, Peoria, Arizona, United States, 85381
Arthritis Association of Southern California, Los Angeles, California, United States, 90015
The Regents of the University of California Los Angeles, Los Angeles, California, United States, 90095
Rheumatology Consultants of Delaware dba Delaware Arthritis, Lewes, Delaware, United States, 19958
Center for Arthritis and Rheumatic Diseases, Miami, Florida, United States, 33157
Coral Research Clinic Corp, Miami, Florida, United States, 33175
Arthritis Research of Florida, Inc, Palm Harbor, Florida, United States, 34684
Sarasota Arthritis Research Center, Sarasota, Florida, United States, 34239
West Broward Rheumatology Associates, Inc, Tamarac, Florida, United States, 33321
North Georgia Rheumatology Group, Lawrenceville, Georgia, United States, 30046
Arthritis Research Center Foundation, NDB, Wichita, Kansas, United States, 67214
Ochsner Clinic Baton Rouge, Baton Rouge, Louisiana, United States, 70809
Ochsner Clinic Foundation, New Orleans, Louisiana, United States, 70121
Rheumatology & Osteoporosis Specialists, Shreveport, Louisiana, United States, 71101
Boston Medical Center, Boston, Massachusetts, United States, 02118
Pine Hollow Partners, East Lansing, Michigan, United States, 48823
St. Paul Rheumatology, Eagan, Minnesota, United States, 55121
University of Nebraska Medical Center, Omaha, Nebraska, United States, 68106
The Center for Rheumatology, LLP, Albany, New York, United States, 12293
Mary Imogene Bassett Hospital, Bassett Research Institute, Cooperstown, New York, United States, 13326
The Ohio State University, Columbus, Ohio, United States, 43203
Oregon Health & Science University, Portland, Oregon, United States, 97239
Altoona Center for Clinical Research, Duncansville, Pennsylvania, United States, 16635
Carolina Health Specialists, Myrtle Beach, South Carolina, United States, 29572
Arthritis Associates, PLLC, Hixson, Tennessee, United States, 37343
West Tennessee Research Institute, Jackson, Tennessee, United States, 38305
Southwest Rheumatology Research, LLC, Mesquite, Texas, United States, 75150
University of Texas Health Science Center at San Antonio, San Antonio, Texas, United States, 78229
West Virginia Research Institute, PLLC, South Charleston, West Virginia, United States, 25309