ClinicaliQ Trial Snapshot
- A Study of Efgartigimod PH20 SC in Children Between 2 and Less Than 18 Years of Age With Generalized Myasthenia Gravis — Recruiting • Phase II • Oncology • NCT06392386.
- Treatment being tested: Efgartigimod PH20 (subcutaneous formulation) – a neonatal Fc receptor (FcRn) inhibitor designed to reduce IgG antibodies in generalized myasthenia gravis (gMG) – is being evaluated for safety, tolerability, pharmacokinetics, pharmacodynamics, and immunogenicity in the pediatric population.
- Patient eligibility overview: Children aged 2 to less than 18 years with confirmed generalized myasthenia gravis are eligible; specific eligibility criteria regarding disease severity, prior treatments, and comorbidities would be detailed in the full protocol.
Use This Page For
- Quick orientation before opening the registry record.
- Checking recruitment status, phase and sponsor at a glance.
- Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying
The purpose of this study is to measure the pharmacokinetics (PK), pharmacodynamics (PD), safety, tolerability, and immunogenicity of efgartigimod PH20 SC in pediatric participants with gMG aged 2 to
Eligibility Snapshot
- : * The participant (and/or their legally authorized representative) understands the requirements of the study and is capable of providing written informed consent/assent and complying with protocol requirements * The participant is aged 2 to
Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.