Healthy and Renal Impairment Study of Colcrys (Colchicine, USP)

Completed · Phase 4

Conditions studied: Pharmacokinetics

In brief

The primary objective of this study is to compare the pharmacokinetic profiles of colchicine and its primary metabolites in plasma and urine following a single 0.6 mg oral dose of colchicine in healthy adults with normal renal function, in patients with mild, moderate or severe renal impairment, and in patients with end-stage renal disease on hemodialysis. An additional objective of this study is to study the clearance of colchicine and its metabolites by hemodialysis. Secondary objectives include evaluation of the safety and tolerability of colchicine in the study population.

Key facts

Study ID
NCT01084278
Run by
Takeda
People needed
40
Starts
2010-05-01
Expected to finish
2011-02-01
Last updated by the study team
2012-10-12

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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