Centre for Human Drug Research
Leiden, 2333, Netherlands
NCT Number: NCT03892902
A clinical study to assess next-day driving performance following evening administrations of ACT-541468 in middle-aged and elderly subjects
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Notify Me50 year–80 year
All sexes
Interventional
Phase 1
Leiden, 2333, Netherlands
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
General criteria:
Study-specific criteria
Exclusion criteria
General criteria:
Study-specific criteria:
Film-coated tablet for oral use at a dose strength of 50 mg.
Over-encapsulated to maintain blinding.
Matching to maintain blinding.
Time frame: On Day 2 at 9 hours post dose. Duration of the test: 1 hour
SDLP = standard deviation of the lateral position
Time frame: On Day 5 at 9 hours post dose. Duration of the test: 1 hour
SDLP = standard deviation of the lateral position
Idorsia Pharmaceuticals Ltd.
Industry
A Single-center, Randomized, Double-blind, Double-dummy, Placebo- and Active-controlled, 4-way Cross-over Study to Assess Next-day Driving Performance Following Single and Multiple Evening Administrations of ACT-541468 in Middle-aged and Elderly Subjects
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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