A81.2
Conditions
Interventions
Group 1: In order to analyze the question we are planning to include 40 patients, which are currently under natalizumab treatment at the department of neurology in the University clinic of Cologne and
Sponsors
Biogen, Inc
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: multiple sclerosis patients under treatment with natalizumab, signed form of consent
Exclusion criteria
Exclusion criteria: consent denied
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Identification of the JCPyVirus in stool, blood and urine samples during treatment with natalizumab. When patients arrive in the clinic to receive their treatement, blood and urine samples will be obtained right away. In the days following the infusion a stool sample will be sent to the clinic by the patient. | — |
Secondary
| Measure | Time frame |
|---|---|
| Quantitative and qualitative analysis of the Virus DNA in the stool, blood and urine samples. | — |
Countries
Germany
Contacts
Public ContactClemens Warnke
University Clinic of Cologne
Outcome results
None listed