Last updated 34 days ago

A Study of Telitacicept for the Treatment of Generalized Myasthenia Gravis (RemeMG)

180 patients around the world
Available in Brazil, Argentina, United States
Myasthenia gravis (MG) is an autoimmune disease that affects the neuromuscular junction on the postsynaptic membrane. The predominant manifestation is muscle weakness, which typically worsens with repeated muscle exertion, such that function is usually the best in the morning with more pronounced weakness at the end of the day. A major challenge in MG is the lack of therapies that cure the disease. Telitacicept is a fully human TACI-Fc fusion protein that targets B-lymphocyte stimulator (BLyS) and A proliferating-inducing ligand (APRIL), neutralizing their interactions with receptors on B cells. The blockage of BLyS and APRIL interaction with their respective cell membrane receptors (transmembrane activator and CAML interactor [TACI], B-cell maturation antigen, and BLyS receptors) by telitacicept would inhibit B-cell proliferation and maturation. This suppression at the proximal portion of the immune response could alleviate autoimmune symptoms. This study is a randomized, double-blind, placebo-controlled Phase 3 study with an open-label extension to evaluate the efficacy and safety of telitacicept in a global patient population with gMG.
RemeGen Co., Ltd.
180Patients around the world

This study is for people with

Myasthenia gravis
Generalized myasthenia gravis

Requirements for the patient

From 18 Years
All Gender

Medical requirements

Male or female patient aged ≥18 years at screening.
Patients have prior confirmed diagnosis of gMG with generalized muscle weakness.
Patients have positive antibodies against AChR or MuSK at screening.
MG-ADL score ≥6 points at screening and baseline with ocular-related score <50% of the total score.
QMG score ≥11 points at screening and baseline.
Patients have been diagnosed with any other autoimmune disease.
Patients having acute or chronic infection.
Patients having thymoma within 5 years or received thymectomy ≤6 months prior to screening.
Patients having current or history of primary immunodeficiency.
Patients having history of malignancy within the last 5 years.
Patient having prior or continuing diagnosis of serious cardiovascular disease.
LinkedinInstagramFacebook
Terms and ConditionsPrivacy Policy