Trial Condition(s):
Evaluation of the positron emission tomography (PET) tracer ZK 6032924 in patients with Multiple Sclerosis compared to healthy volunteers
13101
Not Available
PET (positron emission tomography) imaging with BAY85-8101 for investigation in patients with Multiple Sclerosis compared to healthy volunteers
Healthy volunteers for brain imaging: - males or females, age 20 - 55 years - assessment of the brain MRI as "normal (age-appropriate)" - absence of any sign of CNS disease, no co-medi cation Patients for brain imaging - males or females, age 20 - 55 years - patients with previously diagnosed MS, presenting with acute relapse, without any current immunomodulating therapy for MS ("drug-naïve"), or patients presenting with first clinical episode suggestive of demyelinating disease (Clinically Isolated Syndrome, CIS) - patients with previously diagnosed MS, presenting with acute relapse, receiving currently immunomodulatory therapy exclusively with interferon β - MRI: >/= 2 T2 lesions and >/= 1 Gadolinium- (Gd-) enhancing lesion
Exclusion criteria for all healthy volunteers and patients: - Pregnancy or lactation - Any disease, condition, or concomitant medications that significantly compromises the function of the body systems and could result in excessive accumulation, impaired metabolism, altered excretion of the radiotracer, or might interfere with the conduct of the study or interpretation of the results - other forms of diseases with neuroinflammatory components
Locations | |
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Locations Investigative Site Stockholm, Sweden, 171 76 | Contact Us: E-mail: [email protected] Phone: Not Available |
Locations Investigative Site Heidelberg, Australia, 3084 | Contact Us: E-mail: [email protected] Phone: Not Available |
Open-label, non-randomized, positron emission tomography (PET) imaging study to evaluate a single dose of 140 MBq (ca. 5 mSv) ZK 6032924 (BAY85-8101) for its diagnostic potential in either drug-naïve or specifically (IFN-beta) pretreated patients with Multiple Sclerosis (MS) with acute relapse or patients with clinically isolated syndrome (CIS), compared to healthy volunteers
Trial Type:
Interventional
Intervention Type:
Drug
Trial Purpose:
Diagnostic
Allocation:
Non-randomized
Blinding:
Open Label
Assignment:
Parallel Assignment
Trial Arms:
2