PK, PD, Safety, and Efficacy Study of Gefurulimab in Pediatric Patients With AChR+ Generalized Myasthenia Gravis

Last updated: December 30, 2024
Sponsor: Alexion Pharmaceuticals, Inc.
Overall Status: Active - Recruiting

Phase

3

Condition

Polymyositis (Inflammatory Muscle Disease)

Neuropathy

Sarcopenia

Treatment

Gefurulimab

Clinical Study ID

NCT06607627
D6780C00004
ALXN1720-MG-302
2024-515157-17-00
  • Ages 6-17
  • All Genders

Study Summary

The primary objective of this study is to assess the pharmacokinetics and pharmacodynamics of gefurulimab in pediatric participants with AChR+ gMG for the duration of the study.

Eligibility Criteria

Inclusion

Inclusion Criteria:

United States of America (USA) specific inclusion criterion:

  • Participant must be 12 to < 18 years of age at the time of signing the informedconsent/assent.

  • All participants must be vaccinated against meningococcal infection from serogroupsA, B, C, W, and Y within 3 years and at least 2 weeks prior to the first dose ofstudy intervention administration.

Rest of World (ROW) specific inclusion criteria:

  • Participant must be 6 to < 18 years of age at the time of signing the informedconsent/assent.

  • All participants must be vaccinated against meningococcal infection from serogroupsA, C, W, Y (and B where available) within 3 years prior to study intervention on Day

  1. If vaccination occurs < 2 weeks prior to Day 1, the participants will receiveprophylactic antibiotics for at least 2 weeks after initial meningococcalvaccination for serogroups A,C,W,Y (and B, where available)

Global inclusion criteria:

  • Diagnosis of MG with generalized muscle weakness meeting the clinical criteriadefined by Myasthenia Gravis Foundation of America (MGFA) Class II, III or IV

  • Positive serological test for autoantibodies against AChR

Exclusion

Exclusion Criteria:

  • History of thymectomy, or any other thymic surgery within 12 months prior toScreening

  • Untreated thymic malignancy, carcinoma, or thymoma

  • History of Neisseria meningitidis infection

  • Pregnancy, breastfeeding, or intention to conceive during the course of the study

Study Design

Total Participants: 12
Treatment Group(s): 1
Primary Treatment: Gefurulimab
Phase: 3
Study Start date:
November 13, 2024
Estimated Completion Date:
June 12, 2029

Connect with a study center

  • Research Site

    Joinville, 89202-451
    Brazil

    Site Not Available

  • Research Site

    Salvador, 41253-190
    Brazil

    Site Not Available

  • Research Site

    Sao Jose Do Rio Preto, 15090-000
    Brazil

    Site Not Available

  • Research Site

    Sao Paulo, 05403-000
    Brazil

    Site Not Available

  • Research Site

    São Paulo, 0438-002
    Brazil

    Site Not Available

  • Research Site

    Bydgoszcz, 85-086
    Poland

    Site Not Available

  • Research Site

    Warszawa, 02-097
    Poland

    Site Not Available

  • Research Site

    Łódź, 93-338
    Poland

    Site Not Available

  • Research Site

    Taipei, 11101
    Taiwan

    Site Not Available

  • Research Site

    Washington, District of Columbia 20010
    United States

    Site Not Available

  • Research Site

    Norfolk, Virginia 23507
    United States

    Active - Recruiting

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.