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Special Drug Use Result Survey of IMAAVY in patients with generalized myasthenia gravis (limited to patients who do not sufficiently respond to steroids or immunosuppressants other than steroids)

Special Drug Use Result Survey of IMAAVY in patients with generalized myasthenia gravis (limited to patients who do not sufficiently respond to steroids or immunosuppressants other than steroids) - IMA1L

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000059519
Enrollment
150
Registered
2025-10-29
Start date
2025-11-30
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

generalized myasthenia gravis (limited to patients who do not sufficiently respond to steroids or immunosuppressants other than steroids)

Interventions

None listed

Sponsors

Janssen Pharmaceutical K.K.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who are receiving their first administration of this drug for generalized myasthenia gravis(limited to patients who do not sufficiently respond to steroids or immunosuppressants other than steroids) .

Exclusion criteria

Exclusion criteria: Patients with prior use of IMAAVY

Design outcomes

Primary

MeasureTime frame
1)Occurrence of safety specifications (infections) 2)Relationship between changes in total IgG levels and the occurrence and seriousness of infections 3)Factors that may affect the onset of infection (e.g., onset status by patient background) 4)Incidence of adverse drug reactions

Countries

Japan

Contacts

Public ContactAsami Otsuka

Janssen Pharmaceutical K.K. Medical Affairs Delivery Unit

aotsuka@its.jnj.com070-2668-6638

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026