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The COVID-19 VaccinE Response and Co-Administration in Rheumatology Patients (COVER-CoAd)
The COVID-19 VaccinE Response and Co-Administration in Rheumatology Patients (COVER-CoAd)

NCT05543642

Active Not RecruitingPhase 4

Sponsor: Oregon Health and Science University

Conditions: Rheumatic Diseases

Interventions: Hepatitis A vaccine, Diphtheria, pertussis, and tetanus booster vaccine

Countries: United States

Based on the experience with influenza, pneumococcal, and shingles vaccinations in rheumatic disease populations, it is clear that some disease modifying anti-rheumatic drugs and the immunomodulatory therapies used to treat immune-mediated inflammatory diseases have the capacity to blunt immune responses to COVID-19 vaccines. Several studies have suggested that patients with autoimmune conditions may be at increased risk of poor COVID-19 outcomes. There is an urgent need to better clarify the immunogenicity and safety of COVID-19 vaccines in people living with rheumatic disease who use immunomodulatory therapies. Boosters at annual or other frequency are available, and there is a need to understand whether these vaccines can be given concurrently with other routine vaccines.

Eligibility overview

Sex: ALL

Age: 18 Years to

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria
Inclusion Criteria:

* Patients must meet all of the inclusion criteria at the time of screening
* Must be 18 years of age or older
* Must live in the United States
* Scheduled for SARS-CoV-2 booster vaccination
* Patients in Rheumatic Disease arm (arm 4) must have inflammatory arthritis (e.g. rheumatoid arthritis, psoriatic arthritis, other) and be receiving stable doses of one of the following medication classes: TNF antagonists, B-cell depletion agents, IL-6 inhibitors, JAK inhibitors, IL-12/23 or IL-23 blockers, IL-17 inhibitors, methotrexate, sulfasalazine, leflunamide, or chronic prednisone (\>15mg/day). Stable dosing is defined as no change in dose in the 30 days prior to enrolment.
* For Arms 1-3: patients seen by rheumatologists who do not have active rheumatic disease requiring immunosuppressive therapy. These will include patients with a past history of auto-immune disease that is no longer active, as well as those with other chronic conditions not associated with autoimmune condition such as osteoarthritis, osteoporosis, or other.
* Patients in the Co-administration arms (arms 2 and 3) must meet ACIP recommendations for the use of HAVRIX® (i.e. not previously vaccinated) and BOOSTRIX® (i.e. last immunization \>9 years ago).
* Patients who, in the opinion of the investigator, can and will comply with the requirements of the protocol (e.g. completion of the REDCap/diary cards, capable of receiving text messages and/or have a personal email address, return for follow-up visits).

Exclusion Criteria:

* Active infection with SARS-CoV-2 (symptom onset or first positive test in the 14 days prior to recruitment) / disease
* Any known contraindication to SARS-CoV-2 (booster) vaccination, including severe allergy to vaccine components
* Prior use of adenoviral COVID-19 vaccination
* Known or history of HIV/AIDS
* Currently receiving radiation or chemotherapy for any type of malignancy
* Receipt of any immunizations other than SARS-CoV-2 within two weeks prior planned SARS-CoV-2 vaccination, or scheduled within 10 weeks after visit 1
* Significant underlying illness that would be expected to prevent completion of the study (e.g., life-threatening disease likely to limit survival to \< 1 year)
* Patients who have a previous history of pericarditis/myocarditis associated with vaccination
* Any other reason that, in the opinion of the site investigator, would interfere with required study related evaluations (e.g. uncontrolled comorbidity)
* Prior receipt of any hepatitis A containing vaccine
* Prior receipt of diphtheria, acellular pertussis, or tetanus vaccination within the last 9 years
* History of physician-diagnosed or laboratory confirmed pertussis within the past 5 years; any history of diphtheria, tetanus disease, or hepatitis A.
Locations (7)
  • Northport, Alabama, United States
  • Riverview, Florida, United States
  • Boise, Idaho, United States
  • Clovis, New Mexico, United States
  • Portland, Oregon, United States
  • Duncansville, Pennsylvania, United States
  • Crossville, Tennessee, United States