ConsideRAte Study - Splenic Stimulation for RA
Start Date
10/19/2021
Completion Date
4/1/2032
Summary
This study will evaluate the safety, tolerability, and effects of stimulating the splenic neurovascular bundle (NVB) with the Galvani System, which consists of a lead, implantable pulse generator, external components and accessories. The study will consist of 4 study periods, including a Randomized Control Trial period (Period 1), an Open Label period (Period 2), a Treat-to-target period (Period 3), and a Long-term Follow-up period (Period 4). Participants eligible for implant will have active rheumatoid arthritis (RA) and have an inadequate response or intolerance to at least two biologic Disease Modifying Anti-Rheumatic Drugs (DMARDs) or JAK inhibitors (JAKis). A sufficient number of participants will be enrolled so that approximately 28 participants will undergo device implantation.
Detailed Description
Participants with active rheumatoid arthritis (RA) who receive the implantable system will be randomly assigned to receive either active stimulation or sham-stimulation for 12 weeks (Period 1). Following Period 1, all participants will enter an open label phase (Period 2) during which participants who responded to stimulation will continue on stimulation; whereas participants who received sham stimulation, or were stimulation non-responders, will receive a market-approved RA drug for 12 weeks. At the end of Period 2, participants who respond to their Period 2 therapy but still exhibit signs and symptoms of RA will enter the Treat-to-target period (Period 3); others will proceed to Period 4 (Long-term Follow-up). During the Treat-to-Target period, participants will be treated with dual therapy (stimulation in combination with the market-approved RA drug) for up to 24 weeks. Period 4 provides long term safety follow up for all study participants for a period of 5 years. Participants may receive stimulation in combination with other approved and standard of care therapies, subject to a favorable benefit-risk assessment in the judgement of the treating rheumatologist.
Eligibility Criteria
Age Range: 22 years to 75 years
Interventions
Active Stimulation
Sham Stimulation
Baricitinib
Background Treatment
Conditions
Locations
Pinnacle Research Group, LLC
Anniston, Alabama 36207
United States
Medvin Research - Covina
Covina, California 91722
United States
Medvin Research - Whittier
Whittier, California 90602
United States
The Osteoporosis & Clinical Trials Center
Hagerstown, Maryland 21740
United States
NYU Langone
Brooklyn, New York 11201
United States
Oregon Health & Science University
Portland, Oregon 97239
United States
Altoona Center for Clinical Research
Altoona, Pennsylvania 16635
United States
Arthritis & Rheumatology Institute
Allen, Texas 75013
United States
St. David's Healthcare
Austin, Texas 78705
United States
Tekton Research
Austin, Texas 78745
United States
Metroplex Clinical Research Center
Dallas, Texas 75231
United States
Southwest Rheumatology Research
Mesquite, Texas 75150
United States
Academic Medical Center (AMC) Dept of Rheumatology & Clinical Immunology
Amsterdam,
Netherlands
Maxima Medical Center, MMC
Eindhoven,
Netherlands