A Prospective Longitudinal Study in Adults With Multifocal Motor Neuropathy
Purpose
This prospective longitudinal study will follow participants with Multifocal Motor Neuropathy over time and collect data on their clinical outcomes, quality of life, and use of health care resources. Participants will follow their regular visit schedule with their treating physician, except for an optional second visit occurring 7 to 14 days after the start of the study to collect biomarker data. No IMP will be administered.
Condition
- Multifocal Motor Neuropathy
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Is at least the local legal age of consent for clinical studies when signing the ICF - Is capable of providing signed informed consent and complying with protocol requirements - Has an existing or new diagnosis of MMN made by a neuromuscular specialist or neurologist
Exclusion Criteria
- Is currently participating in any clinical study with an IMP - Has other medical conditions that could affect the assessment of MMN
Study Design
- Phase
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Recruiting Locations
The University of Kansas Health System - Landon Center on Aging
Kansas City, Kansas 66103
Kansas City, Kansas 66103
More Details
- Status
- Recruiting
- Sponsor
- argenx