๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-07-28

A Study to Investigate the Efficacy, Safety and Tolerability of Remibrutinib Versus Placebo in Adult Patients With Generalized Myasthenia Gravis (NCT06744920)

A Randomized, Double-blind, Placebo-controlled Phase III Study to Evaluate the Efficacy, Safety, and Tolerability of Remibrutinib in Patients With Generalized Myasthenia Gravis, Followed by an Open-label Extension Phase

๐ŸŸข Recruiting Phase3 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Novartis Pharmaceuticals

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

A study to evaluate the efficacy, safety and tolerability of Remibrutinib versus placebo in adult patients with Generalized Myasthenia Gravis who are on stable, standard-of-care (SOC) treatment.

Who can join: Review the eligibility criteria below.

Location: Neuromuscular Research Center โ€” Phoenix, Arizona

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 (130 Sites)

Showing the first 25 of 130 sites.

  • Neuromuscular Research Center โ€” Phoenix, Arizona
  • Honor Health Research Institute โ€” Scottsdale, Arizona
  • Fullerton Neuro and Headache Ctr โ€” Fullerton, California
  • University Of Southern California โ€” Los Angeles, California
  • Univ Cali Irvine ALS Neuromuscular โ€” Orange, California
  • California Pacific Medical Center โ€” Sacramento, California
  • Medstar Washington Hospital Center โ€” Washington D.C., District of Columbia
  • SFM Clinical Research LLC โ€” Boca Raton, Florida
  • Homestead Assoc In Research Inc โ€” Homestead, Florida
  • Neurology Associates PA โ€” Maitland, Florida
  • AdventHealth โ€” Orlando, Florida
  • Neurological Services of Orlando PA โ€” Orlando, Florida
  • University of Chicago Medical Centr โ€” Chicago, Illinois
  • Mid Atlantic Epilepsy and Sleep Ctr โ€” Bethesda, Maryland
  • Massachusetts General Hospital โ€” Boston, Massachusetts
  • Michigan State University-Department of Neurology โ€” East Lansing, Michigan
  • Dent Neurological Institute โ€” Buffalo, New York
  • Univ of Cincinnati Medical Center โ€” Cincinnati, Ohio
  • Cleveland Clinic Foundation โ€” Cleveland, Ohio
  • University of Pittsburgh Medical Center โ€” Pittsburgh, Pennsylvania
  • Houston Methodist Hospital โ€” Houston, Texas
  • UT Health Science Center โ€” Houston, Texas
  • University of WA Division of Cardio โ€” Seattle, Washington
  • Center for Neurological Disorders G โ€” Greenfield, Wisconsin
  • Novartis Investigative Site โ€” Rosario, Santa Fe Province

๐Ÿ“ž Contact the Study Coordinator

Phone: (888) 669-6682

Email: novartis.email@novartis.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†—