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Renal Impairment clinical trials

View clinical trials related to Renal Impairment.

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NCT ID: NCT01904214 Completed - Renal Impairment Clinical Trials

A Single-dose, Open-label, Parallel-group Study to Assess the Pharmacokinetics of BAF312 in Subjects With Renal Impairment Compared to Subjects With Normal Renal Function

Start date: July 2013
Phase: Phase 1
Study type: Interventional

to quantify the effect of different degrees of renal impairment on the pharmacokinetics of BAF312 (and selected metabolites) and to assess safety and tolerability in order to develop dosing recommendations for subjects with renal impairment

NCT ID: NCT01796938 Completed - Healthy Clinical Trials

Study to Evaluate the Pharmacokinetics, Safety, Tolerability of Single Dose Lacosamide in Subjects With Renal Impairment Compared to Healthy Subjects

Start date: June 2004
Phase: Phase 1
Study type: Interventional

To investigate the Pharmacokinetics (PK) of oral administered Lacosamide in renal impaired subjects and healthy subjects.

NCT ID: NCT01770652 Completed - Renal Impairment Clinical Trials

An Open-label, Non-randomized, Parallel Group Study in Subjects With Mild, Moderate, Severe, or No Renal Impairment

Start date: January 2013
Phase: Phase 4
Study type: Interventional

Multi-center, non-randomized, open-label, single-dose, parallel group study to determine the effect of impaired renal function on the PK of deferiprone and its 3-O-glucuronide metabolite following a single oral dose of 33mg/kg Ferriprox®.

NCT ID: NCT01763190 Completed - Renal Impairment Clinical Trials

Open Label Pharmacokinetic Study of SAR302503 in Subjects With Renal Impairment

Start date: November 2012
Phase: Phase 1
Study type: Interventional

Primary Objective: To study the effect of mild, moderate and severe renal impairment on the pharmacokinetics of SAR302503. Secondary Objective: To assess the tolerability of SAR302503 given as a single 300 mg dose in subjects with mild, moderate and severe renal impairment and in matched subjects with normal renal function.

NCT ID: NCT01761773 Completed - Healthy Clinical Trials

A Single-Dose Study to Assess the Pharmacokinetics of Cabozantinib (XL184) Capsules in Subjects With Impaired Renal Function

Start date: December 2012
Phase: Phase 1
Study type: Interventional

The main objective of the trial is to compare the pharmacokinetics of a 60 mg dose of cabozantinib in adult subjects with impaired renal function compared with healthy adult subjects. Another objective is to assess the safety and tolerability of cabozantinib in these adult subjects.

NCT ID: NCT01740362 Completed - Renal Impairment Clinical Trials

Pharmacokinetics Of CP-690,550 In Patients With Impaired Renal Function

Start date: October 2003
Phase: Phase 1
Study type: Interventional

A study to evaluate the pharmacokinetics of CP-690,550 in subjects with mild, moderate or severe renal impairment, who do not require hemodialysis, compared to healthy controls.

NCT ID: NCT01729364 Completed - Renal Impairment Clinical Trials

Fluid Investigation Colloid vs Crystalloid Reg. Renal Hemodynamics and Function

Start date: April 2008
Phase: N/A
Study type: Interventional

Comparing the effects of crystalloid versus colloid fluid resuscitation in CABG patients postoperatively regarding renal blood flow, glomerular filtration rate and renal oxygen demand.

NCT ID: NCT01619033 Completed - Renal Impairment Clinical Trials

Pharmacokinetics of BF2.649 in Renal Impairment

Start date: July 2011
Phase: Phase 1
Study type: Interventional

This is an open, parallel group study in subjects with normal renal function compared to those with renal dysfunction.

NCT ID: NCT01613690 Completed - Renal Impairment Clinical Trials

Comparing the Pharmacokinetics, Safety and Tolerability of NVA237 in Renal Impairment

Start date: June 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to see how the body processes and gets rid of NVA237 in people who have impaired kidney function compared to people whose kidney function is normal.

NCT ID: NCT01578928 Completed - Renal Impairment Clinical Trials

A Phase l Study to Evaluate the Pharmacokinetics and Safety Pasireotide in Subjects With Varying Degrees of Renal Impairment Compared to Healthy Volunteers

Start date: May 2012
Phase: Phase 1
Study type: Interventional

The purpose of this study is to assess the effect of renal impairment on the pharmacokinetics (PK) of pasireotide,the PK of pasireotide in subjects with different degrees of renal impairment.