RecruitingPhase 2NCT07501702

A Phase 2 Study to Evaluate Povetacicept in Adults With Generalized Myasthenia Gravis

A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study With a Long-term Extension of Povetacicept in Adults With Generalized Myasthenia Gravis


Sponsor

Vertex Pharmaceuticals Incorporated

Enrollment

30 participants

Start Date

May 13, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to evaluate the pharmacodynamic (PD) effect, safety, and tolerability of Povetacicept in participants with generalized myasthenia gravis (gMG).


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Inclusion Criteria2

  • Age 18-80 years
  • Diagnosis of generalized myasthenia gravis with generalized muscle weakness and fitting MGFA clinical classification II-IV

Exclusion Criteria2

  • History of thymic surgery within 6 months of screening
  • History of malignancy within the last 5 years

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Interventions

DRUGPovetacicept

Solution for Subcutaneous Injection.

DRUGPlacebo

Solution for Subcutaneous Injection.


Locations(11)

Neurology Offices

Boca Raton, Florida, United States

SFM Clinical Reseach, LLC

Boca Raton, Florida, United States

Homestead Associates in Research

Homestead, Florida, United States

Quantix Research

Miami, Florida, United States

Hawaii Pacific Neuroscience

Honolulu, Hawaii, United States

HSHS Medical Group - St. Elizabeth's Hospital

O'Fallon, Illinois, United States

Las Vegas Neurology Center

Las Vegas, Nevada, United States

Clinical Trials of South Carolina - Neurology

Charleston, South Carolina, United States

Nerve and Muscle Center of Texas - Neurology

Houston, Texas, United States

Texas Institute for Neurological Disorders

Sherman, Texas, United States

Neurology Care Clinic

Waxahachie, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT07501702


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