MG0008

An open-label Extension study to evaluate rozanolixizumab in pediatric study participants with generalized myasthenia gravis

Brief summary

The purpose of the study is to assess the long term safety and tolerability of additional 6-week treatment cycles with rozanolixizumab in pediatric participants with generalized Myasthenia Gravis (gMG) aged ≥2 at the time of the Screening Visit of MG0006.

Medical Condition

Generalized Myasthenia Gravis

Min. Age

2
Years

Max. Age

-

Who Can Join?

All

Status

Enrolling by invitation
Inclusion criteria

Study participant must meet one of the following: - Study participant completed MG0006 according to the protocol - Study participant completed the MG0006 Treatment Period and has a worsening of generalized myasthenia gravis (gMG) symptoms in the Observation Period of MG0006

Exclusion criteria

- Study participant met any mandatory withdrawal or mandatory permanent investigational medicinal product (IMP) discontinuation criteria in MG0006 or permanently discontinued IMP - Study participant has a known hypersensitivity to any components of the IMP or other neonatal Fc receptor (FcRn) drugs - Study participant has any laboratory abnormality that, in the opinion of the Investigator, is clinically significant, has not resolved at Baseline, and could jeopardize or compromise the study participant’s ability to participate in this study

Study Medication Description

Study Medication:

RYSTIGGO

Other Descriptive Name:

rozanolixizumab

Placebo

No

Comparator:

No

Study Dates

October 2024

Actual Start Date of Enrollment

August 2027

Planned Study Completion Date

General Information

Study ID:
MG0008
CT.gov Number:
Phase:
Phase 3

Locations

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