Dose-response Study of Paricalcitol Injection in Chronic Kidney Disease Patients Receiving Hemodialysis

PHASE2CompletedINTERVENTIONAL
Enrollment

153

Participants

Timeline

Start Date

April 30, 2008

Primary Completion Date

March 31, 2009

Study Completion Date

March 31, 2009

Conditions
Chronic Kidney Disease on HemodialysisSecondary Hyperparathyroidism
Interventions
DRUG

Maxacalcitol

Study drug was administered 3 times per week (no more frequently than every other day) intravenously immediately before the completion of hemodialysis. The initial dosage was administered for 2 weeks, with subsequent dosage adjustment based on the subject's iPTH, calcium (adjusted), and phosphorus levels every 2 weeks. Total duration of treatment was 12 weeks.

DRUG

Paricalcitol

Study drug was administered 3 times per week (no more frequently than every other day) intravenously immediately before the completion of hemodialysis. The initial dosage was administered for 2 weeks, with subsequent dosage adjustment based on the subject's iPTH, calcium (adjusted), and phosphorus levels every 2 weeks. Total duration of treatment was 12 weeks.

Trial Locations (12)

Unknown

Tokyo

Aichi

Chiba

Fukuoka

Hokkaido

Ibaraki

Kanagawa

Kumamoto

Nagano

Nagasaki

Osaka

Saitama

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Abbott Japan Co.,Ltd

INDUSTRY

lead

Abbott

INDUSTRY

NCT00667576 - Dose-response Study of Paricalcitol Injection in Chronic Kidney Disease Patients Receiving Hemodialysis | Biotech Hunter | Biotech Hunter