Parkinson Disease Clinical Trial
Official title:
A Randomized, Placebo-controlled, Parallel Group, Patient-blinded, Multi-center, Phase I Pilot Study to Assess Tolerability and Safety of Two Doses of AFFITOPE® PD03A Formulated With Adjuvant to Patients With Early Parkinson's Disease
Study AFF011 is a randomized controlled parallel Group phase I study to investigate the
safety and tolerability of two doses of the vaccine AFFITOPE® PD03A given to patients with
early Parkinson's disease.
In total 36 patients will be enrolled in 3 independent groups (2 treatment groups, 1 Placebo
group), each consisting of 12 patients. The patients will be randomized to either receive
15µg or 75µg AFFITOPE® PD03A formulated with adjuvant or the reference substance without
active component (Placebo). Over a study duration of 52 weeks, the study participants
receive 4 injections as basic immunization in a 4-weekly interval and 1 boost immunization
36 weeks after the first injection. Male and female patients aged 45 to 70 years can
participate in the trial. 2 study sites in Austria (Innsbruck and Vienna) will be involved.
AFF011 is part of a project SYMPATH funded by the European Commission
(FP7-HEALTH-2013-INNOVATION-1 project; N° HEALTH-F4-2013-602999).
n/a
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
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