Back to Trials
NCT05003310NARecruiting

ConsideRAte Study - Splenic Stimulation for RA

Galvani Bioelectronics

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

Inclusion Criteria: * RA of at least six months duration, per 2010 ACR/EULAR criteria * Male or female participants, 22-75 years of age * Active RA * Inadequate Response to at least 2 biologic DMARDs and/or JAK-inhibitors (JAKis) including at least one TNF inhibitor * Have an appropriate washout from previously used biological DMARDs or JAKi * Receiving current treatment with standard dose(s) of conventional synthetic DMARD(s) or have documented history of failure due to ineffectiveness or intolerance Exclusion Criteria: * Inability to provide informed consent * Significant psychiatric disease or substance abuse * History of unilateral or bilateral vagotomy * Active or latent tuberculosis * Known infection with human immunodeficiency virus (HIV); current acute or chronic hepatitis B or hepatitis C; previous hepatitis B * Positive SARS COV 2 PCR screening test for COVID-19 infection (at the point of screening for this study) * Currently implanted electrically active medical devices (e.g., cardiac pacemakers, automatic implantable cardioverter-defibrillators) * Previous splenectomy

Interventions

DEVICE

Active Stimulation

DEVICE

Sham Stimulation

DRUG

Baricitinib

DRUG

Background Treatment

Interested in This Trial?

Contact the trial locations directly using the information below to learn more about enrollment.

Expressing interest lets you review the study and consent before we connect you with the research site.

Conditions

Rheumatoid Arthritis

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