The purpose of this study is to evaluate the safety and tolerability of multiple ascending doses of ORM-12741.
The purpose is to evaluate the safety, tolerability and pharmacokinetics of escalating multiple doses of ORM-12741 in healthy volunteers.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
49
Ascending multiple doses to sequential panels
Forenap Pharma
Rouffach, France
Safety measures, i.e. assessing adverse events, vital signs, ECG, safety laboratory values
Time frame: 12 days
Pharmacokinetic profile (Cmax, tmax, t1/2, AUC, PTF) of ORM-12741 and its metabolites
Time frame: PK samples will be collected for 12 days
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