The purpose of this study is to evaluate the pharmacokinetics properties of idalopirdine following multiple dosing in patients with renal impairment and compare to those in healthy subjects
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
16
encapsulated film-coated tablets for oral use once daily for 10 days
DE801
München, Germany
Area under the LuAE58054 plasma concentration-time curve from time zero to 24h(AUC0-24)
Time frame: Day 10
Maximum observed concentration (Cmax) of Lu AE58054
Time frame: 0-12 hours day 10
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.