Overview

A Study To Investigate The Effects Of End Stage Renal Disease And Hemodialysis On The Pharmacokinetics Of Ropinirole

Status:
Completed
Trial end date:
2006-12-01
Target enrollment:
0
Participant gender:
All
Summary
This study will investigate the effects of severe renal impairment and hemodialysis on the characteristics of the drug, ropinirole.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
GlaxoSmithKline
Treatments:
Ropinirole
Criteria
Inclusion:

- Patients and subjects between 18-79 years old.

- End stage renal patients who are consistently receiving dialysis for a minimum of 3.5
hours, three times per week, with hemodialysis blood flow rates of >200mL/min may be
eligible to enter the study.

- Patients must also have systolic blood pressure 100-190mmHg and diastolic blood
pressure <120mmHg.

- Healthy subjects must have systolic blood pressure 100-150mmHg.

Exclusion:

- Female subjects who are pregnant and/or breast-feeding must not participate in this
study.