๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-07-31

Study of Aritinercept in Patients With Generalized Myasthenia Gravis (NCT07596901)

A Double-Blind, Randomized, Placebo-Controlled Study to Investigate the Safety and Efficacy of Aritinercept, a Dual BAFF/APRIL Inhibitor, in Patients With Generalized Myasthenia Gravis

๐ŸŸข Recruiting Phase1 / Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Aurinia Pharmaceuticals Inc.

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

This clinical study will enroll patients with generalized myasthenia gravis (gMG). The goal of this clinical study is to assess the safety, tolerability, effectiveness, pharmacokinetics (how the body processes the drug) and pharmacodynamics (how the drug affects the body) of aritinercept.

Who can join: Review the eligibility criteria below.

Location: Aurinia Investigational Site โ€” Pasadena, California

Age range: 18 Years to 85 Years

๐Ÿงช Interventions in This Study

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (11 Sites)

  • Aurinia Investigational Site โ€” Pasadena, California
  • Aurinia Investigational Site โ€” Altamonte Springs, Florida
  • Aurinia Investigational Site โ€” Boca Raton, Florida
  • Aurinia Investigational Site โ€” Homestead, Florida
  • Aurinia Investigational Site โ€” Miami, Florida
  • Aurinia Investigational Site โ€” Miami, Florida
  • Aurinia Investigational Site โ€” Chicago, Illinois
  • Aurinia Investigational Site โ€” O'Fallon, Illinois
  • Aurinia Investigational Site โ€” Dearborn, Michigan
  • Aurinia Investigational Site โ€” Flint, Michigan
  • Aurinia Investigational Site โ€” Houston, Texas

๐Ÿ“ž Contact the Study Coordinator

Phone: (833) 606-5975

Email: clinicaltrials@auriniapharma.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—