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Clinical Trials/NCT00701662
NCT00701662
Completed
Phase 2

A Multicentre Study of Subcutaneous Immunoglobulin (SCIG) in Patients With Multifocal Motor Neuropathy (MMN)

CSL Behring3 sites in 3 countries8 target enrollmentNovember 2007

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Multifocal Motor Neuropathy (MMN)
Sponsor
CSL Behring
Enrollment
8
Locations
3
Primary Endpoint
Mean Overall MRC Score at Baseline and Week 24
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

The objective of this study is to assess efficacy, safety, and convenience of purified human antibodies administered under the skin in the treatment of MMN patients.

Registry
clinicaltrials.gov
Start Date
November 2007
End Date
January 2009
Last Updated
12 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with documented clinical diagnosis and electrophysiological evidence of MMN
  • Patients who have previously responded to intravenous immunoglobulin (IVIG) and have been on stable treatment with IVIG for at least 12 weeks prior to screening
  • Patients treated with the equivalent of ≥0.4g/kg body weight (bw) IVIG per month
  • Provision of informed consent by patient

Exclusion Criteria

  • Aspartate aminotransferase (ASAT) or alanine aminotransferase (ALAT) concentration \>2.5 times the upper normal limit (UNL)
  • Creatinine concentration \>1.5 times the UNL
  • Known allergic reactions to blood products
  • Any skin disease interfering with the assessment of injection site reactions
  • Any other medical condition, which in the opinion of the investigator, might interfere with successful completion of the protocol
  • Any condition likely to interfere with the evaluation of the study drug or satisfactory conduct of the trial
  • Participation in a study with an investigational drug within three months prior to enrolment
  • Patients treated with the equivalent of \>2.0g/kg bw IVIG per month

Outcomes

Primary Outcomes

Mean Overall MRC Score at Baseline and Week 24

Time Frame: Baseline and week 24

The 200-point MRC sum score is the sum of scores for 20 bilateral (left and right side) muscle groups, each rated between 0 (no movement) to 5 (normal movement/power). A higher MRC sum score indicates greater muscle contraction/limb movement.

Change From Baseline to Week 24 in Muscle Strength

Time Frame: Baseline to week 24

The change in Medical Research Council (MRC) score was determined at week 24 compared to baseline using descriptive statistics and nonparametric, two-sided 95% confidence intervals based on the Hodges-Lehmann method. Data for one of the eight subjects was from week 13 as week 24 data were not available. The 200-point MRC sum score is the sum of scores for 20 bilateral (left and right side) muscle groups, each rated between 0 (no movement) to 5 (normal movement/power). A higher MRC sum score indicates greater muscle contraction/limb movement. Positive values for change in MRC sum score indicate improvement, with a more positive value indicating greater muscle contraction/ limb movement compared with the value at baseline.

Secondary Outcomes

  • Treatment Satisfaction at Baseline and Week 25(At baseline and week 25)
  • Change From Baseline to the Completion Visit in Motor Function(Baseline to the completion visit (up to week 25))
  • Change From Baseline to Week 24 in Disability(Baseline to week 24)
  • Mean Disability Score at Baseline and Week 24(Baseline and Week 24)
  • Health-Related Quality of Life at Baseline and Week 25(At baseline and week 25)
  • Mean Motor Function Score at Screening and Week 25(Screening and week 25)
  • Overall Health Status at Baseline and Week 25(Baseline and week 25)
  • Number of Patients With Adverse Events (AEs) by Severity and Relatedness(For the duration of the study, up to Week 25)
  • Rate of AEs by Severity and Relatedness(For the duration of the study, up to Week 25)
  • Number of Patients With Local/Injection Site Reactions(For the duration of the study, up to Week 25)
  • Number of Patients With Clinically Relevant Changes in Vital Signs(Baseline to Week 25)
  • Number of Patients With Clinically Relevant Changes in Laboratory Parameters(Baseline to Week 25)

Study Sites (3)

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