Recruiting
Phase 3

Telitacicept

Sponsor:

Vor Biopharma

Code:

NCT06456580

Conditions

Generalized Myasthenia Gravis

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Telitacicept

Placebo

Study Details

Brief summary:

The purpose of this study is to evaluate the efficacy and safety of telitacicept in the treatment of generalized myasthenia gravis.

Conditions

Generalized Myasthenia Gravis

Study ID

NCT06456580

Start date

Jul 17, 2024

Status verified date

May, 2026

Completion date

Jan, 2029

Anticipated

Primary completion date

May, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Key Inclusion Criteria:

1. Male or female patient aged ≥18 years at screening.
2. Patients have prior confirmed diagnosis of gMG with generalized muscle weakness (typical pattern of weakness meeting the clinical criteria for diagnosis of MG as defined by the Myasthenia Gravis Foundation of America (MGFA) clinical classification II-IV.
3. Patients have positive antibodies against AChR or MuSK at screening.
4. MG-ADL score ≥6 points at screening and baseline with ocular-related score <50% of the total score.
5. QMG score ≥8 points, and ≥ 4 items score at least 2 points at screening and baseline.

Key Exclusion Criteria:

1. Patients have been diagnosed with any other autoimmune disease which can potentially pose a safety or efficacy confounding risk.
2. Patients having acute or chronic infection.
3. Patients having thymoma within 5 years or received thymectomy ≤6 months prior to screening. Patients with thymoma diagnosed 3-5 years prior to screening may be eligible if thymoma was at a localized stage and definitively treated with complete surgical resection.
4. Patients having current or history of primary immunodeficiency.
5. Patients having history of malignancy within the last 5 years.
6. Patient having prior or continuing diagnosis of serious cardiovascular, liver, kidney, respiratory system, endocrine or hematologic disease.

Study Design

Enrollment

180 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Telitacicept

Telitacicept

placebo comparator: Placebo

Placebo

Interventions

Telitacicept

Subcutaneous injection

Placebo

Subcutaneous injection

Primary outcome measure

  • Change from baseline in Myasthenia Gravis-Activities of Daily Living (MG-ADL) score at Week 24 [ Time Frame: Week 24 ]

Central Contacts and Locations

Central contacts

Locations

HonorHealth Neurology - Bob Bové Neuroscience Institute

Recruiting

Scottsdale, Arizona, United States, 85258

University of Southern California

Recruiting

Los Angeles, California, United States, 90033

University of California Irvine

Recruiting

Orange, California, United States, 92868

University of California San Francisco (UCSF)

Recruiting

San Francisco, California, United States, 94143

SFM Clinical Research

Recruiting

Boca Raton, Florida, United States, 33487

Allied Biomedical Research Institute (ABRI)

Recruiting

Miami, Florida, United States, 33155

Medsol Clinical Research Center

Recruiting

Port Charlotte, Florida, United States, 33952

University of South Florida Health (USF Health)

Recruiting

Tampa, Florida, United States, 33613

Wellstar MCG Health Medical Center

Recruiting

Augusta, Georgia, United States, 30912

Hospital Sisters Health System Medical

Recruiting

O'Fallon, Illinois, United States, 62269

University of Kansas Medical Center

Recruiting

Kansas City, Kansas, United States, 66160

University of Kentucky

Recruiting

Lexington, Kentucky, United States, 40506

University of Louisville Physicians

Recruiting

Louisville, Kentucky, United States, 40202

Neurology Center of New England

Recruiting

Foxborough, Massachusetts, United States, 02035

Contacts

Michigan State University Clinical Center

Recruiting

East Lansing, Michigan, United States, 48824

Trinity Health - Grand Rapids Hospital

Recruiting

Grand Rapids, Michigan, United States, 49503

UM Health Care - Neurology and Sleep Disorders Clinic

Recruiting

Columbia, Missouri, United States, 65212

Hospital for Special Surgery

Recruiting

New York, New York, United States, 10021

Mount Sinai Health System

Recruiting

New York, New York, United States, 10029

Montefiore Medical Center

Recruiting

The Bronx, New York, United States, 10467

University of North Carolina Hospitals - Neurology Clinic

Recruiting

Chapel Hill, North Carolina, United States, 27517

University of Cincinnati Health Physicians - Clifton

Recruiting

Cincinnati, Ohio, United States, 45219

Empower Clinical Research

Recruiting

Tigard, Oregon, United States, 97223

University of Texas Southwestern Medical Center

Recruiting

Dallas, Texas, United States, 75390

Houston Methodist Neurological Institute

Recruiting

Houston, Texas, United States, 77030

Center for Neurological Disorders, S.C. - Greenfield - Gamma Therapeutic Center

Recruiting

Greenfield, Wisconsin, United States, 53228

University Hospital - London Health Sciences Centre

Recruiting

London, Ontario, Canada, N6C 2R5

More Information

Sponsor

Vor Biopharma

Last update posted

Jun 18, 2026

Last verified

May, 2026

Keywords

  • Myasthenia Gravis
  • gMG

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by Vor Biopharma on 2026-06-18.