G35
Conditions
Interventions
Group 1: We will include 20 multiple sclerosis patients that are planned for alemtuzumab therapy in our study.
For one year we will analyze monthly additional lab parameters during the mandatory bloo
Sponsors
Universitätsklinikum Köln
Eligibility
Sex/Gender
All
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Multiple Sclerosis patients starting therapy with alemtuzumab
Exclusion criteria
Exclusion criteria: revocation of consent and underage patients
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Analysis of innate immune cells and inflammatory mediators after Alemtuzumab therapy (primary endpoint: macrophage populations, macrophage polarizations with immunohistochemistry and flow cytomerty, | — |
Secondary
| Measure | Time frame |
|---|---|
| secondary endpoint: inflammatory parameters and mediators in the blood) | — |
Countries
Germany
Contacts
Public ContactHelmar Lehmann
Universitätsklinikum Köln
Outcome results
None listed