The purpose of this study is to evaluate the safety and tolerability of escalating doses of ORM-12741 in healthy volunteers.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
120
Alternating panel single dose escalation.
Forenap Pharma
Rouffach, France
Safety measures, i.e. assessing adverse events, vital signs, ECG, safety laboratory values
Time frame: About 8 weeks
Pharmacokinetics
Time frame: 5 days after each dose
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.