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Open-label Uncontrolled Trial to Evaluate Pharmacokinetics, Pharmacodynamics, Safety, and Activity of Efgartigimod in Children From 2 to Less Than 18 Years of Age With Generalized Myasthenia Gravis

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-513854-31-00
Acronym
ARGX-113-2006
Enrollment
12
Registered
2024-06-24
Start date
2021-10-27
Completion date
Unknown
Last updated
2025-11-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Generalized Myasthenia Gravis

Brief summary

Efgartigimod concentrations as input for compartmental, model-driven analysis to determine age and size dependency of clearance and volume of distribution, PD parameters: total IgG levels and anti-acetylcholine receptors antibodies (AChR-Ab) as input for PK/PD modeling analysis

Detailed description

Incidence and severity of AEs, incidence of serious AEs (SAEs), incidence of AEs of special interest (AESIs), and changes in laboratory test results, physical examination results, vital sign measurements, and electrocardiogram (ECG) (part B only for ECGs), Efgartigimod serum concentrations, Levels of total IgG and AChR-Ab: absolute values, change from baseline and percent (%) change from baseline, Incidence and prevalence of antidrug antibodies (ADAs) against efgartigimod, MG-ADL total score: absolute value and change from baseline total MG-ADL score, Total QMG score: absolute value and change from baseline, Total score EQ-5D-Y: absolute value and change from baseline, Quality of Life in Neurological Disorders (Neuro-QoL) Pediatric Fatigue Score: values and change from baseline, Change in protective antibody titers to vaccines received before or received during the trial

Interventions

Sponsors

Argenx
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
0 Years to 17 Years

Design outcomes

Primary

MeasureTime frame
Efgartigimod concentrations as input for compartmental, model-driven analysis to determine age and size dependency of clearance and volume of distribution, PD parameters: total IgG levels and anti-acetylcholine receptors antibodies (AChR-Ab) as input for PK/PD modeling analysis

Secondary

MeasureTime frame
Incidence and severity of AEs, incidence of serious AEs (SAEs), incidence of AEs of special interest (AESIs), and changes in laboratory test results, physical examination results, vital sign measurements, and electrocardiogram (ECG) (part B only for ECGs), Efgartigimod serum concentrations, Levels of total IgG and AChR-Ab: absolute values, change from baseline and percent (%) change from baseline, Incidence and prevalence of antidrug antibodies (ADAs) against efgartigimod, MG-ADL total score: absolute value and change from baseline total MG-ADL score, Total QMG score: absolute value and change from baseline, Total score EQ-5D-Y: absolute value and change from baseline, Quality of Life in Neurological Disorders (Neuro-QoL) Pediatric Fatigue Score: values and change from baseline, Change in protective antibody titers to vaccines received before or received during the trial

Countries

Belgium, France, Germany, Italy, Netherlands, Poland, Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026