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Active, not recruiting Phase 2

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

NCT07501702 · tracked via the Priya Life Science UK tracker
Phase
Phase 2
Started
2026-05-13
Last updated
2026-10-29

Condition(s) studied

Myasthenia Gravis, Generalized

Investigational drug(s) / intervention(s)

Povetacicept →Placebo

Povetacicept: Solution for Subcutaneous Injection.

Placebo: Solution for Subcutaneous Injection.

Study 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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Key Inclusion Criteria: * Age greater than or equal to (\>=) 18 years * Diagnosis of generalized myasthenia gravis with generalized muscle weakness and fitting MGFA clinical classification II-IV * Additional inclusion criteria are defined in the protocol Key Exclusion Criteria: * History of thymic surgery within 6 months of screening * History of malignancy within the last 5 years * Additional exclusion criteria are defined in the protocol Other protocol defined Inclusion/Exclusion criteria will apply.

Primary outcome measure(s)

  • Percent change in Total Immunoglobulin G (IgG) — Baseline and At Week 12
  • Safety and Tolerability as Assessed by Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs) — From Baseline Up to Week 116

Trial sites (31)

FacilityCityRegionStatus
Tri Valley Neurology Medical Associates Inc. Mission Hills California
Neurology Offices Boca Raton Florida
SFM Clinical Reseach, LLC Boca Raton Florida
Homestead Associates in Research Homestead Florida
UF Health Jacksonville Respiratory Therapy (PFT and DLCO) Jacksonville Florida
Y & L Advance Health Care, Inc D/B/A Elite Clinical Research - Neurology Miami Florida
Quantix Research Miami Florida
USF Carol and Frank Morsani Center for Advanced Healthcare Tampa Florida
Patient Care Clinical Research, LLC Snellville Georgia
Hawaii Pacific Neuroscience Honolulu Hawaii
HSHS Medical Group - St. Elizabeth's Hospital O'Fallon Illinois
Las Vegas Neurology Center Las Vegas Nevada
Univ of NC Chapel Hill, Neurology Chapel Hill North Carolina
Clinical Trials of South Carolina - Neurology Charleston South Carolina
Ut Erlanger Neurology Chattanooga Tennessee
Nerve and Muscle Center of Texas - Neurology Houston Texas
Texas Institute for Neurological Disorders Sherman Texas
Neurology Care Clinic Waxahachie Texas
Eastern Health - Box Hill Hospital Box Hill Australia
MICS Centrum Medyczne Bydgoszcz Bydgoszcz Poland
Neurologia Slaska Centrum Medyczne Katowice Poland
Clinical Research Center Sp. z o.o., Medic-R Sp. K. Poznan Poland
NZOZ NEURO-KARD Ilkowski i Partnerzy Sp. Partnerska Lekarzy Poznan Poland
Twoja Przychodnia Poznanskie Centrum Medyczne Sp. z o. o. Poznan Poland
Centrum Medyczne Neuroprotect Warsaw Poland
ETG Neuroscience Warsaw Poland
Istanbul University Medical Faculty Fatih Turkey (Türkiye)
Kocaeli University Medical Faculty Kocaeli Turkey (Türkiye)
University Hospitals Birmingham NHS Foundation Trust - Queen Elizabeth Hospital Birmingham United Kingdom
St. George's University Hospital London United Kingdom
Northern Care Alliance NHS Foundation Trust - Salford Royal Hospital Salford United Kingdom
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07501702 on ClinicalTrials.gov ↗ ← All trials in the UK