LEO 27847 - Safety, Tolerability, Pharmacokinetic & Pharmacodynamic Study

See also
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Completed	`NCT01220050` - Paricalcitol in Reducing Parathyroid Hormone Levels and Ameliorating Markers of Bone Remodelling in Renal Transplant Recipients With Secondary Hyperparathyroidism	Phase 2
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Completed	`NCT00117052` - SENSOR: Study to Investigate Cinacalcet Treatment in Haemodialysis Patients With Secondary Hyperparathyroidism	Phase 3
Completed	`NCT03626948` - SK-1403 Long-term Treatment Study; Long-term Study in Patients With Secondary Hyperparathyroidism Receiving Hemodialysis	Phase 3
Completed	`NCT01382212` - A Study to Evaluate the Safety of Paricalcitol Capsules in Pediatric Subjects Ages 10 to 16 With Stage 5 Chronic Kidney Disease Receiving Peritoneal Dialysis or Hemodialysis	Phase 3
Completed	`NCT01224782` - Evaluation of Treatment With Zemplar Capsules in the Therapy of Secondary Hyperparathyroidism (SHPT)	N/A
Completed	`NCT01219855` - Safety/Efficacy Study of CTAP101 in Chronic Kidney Disease Subjects With Secondary Hyperparathyroidism (SHPT)	Phase 2/Phase 3
Completed	`NCT00990704` - Paricalcitol Compared to Maxacalcitol in Chronic Kidney Disease Patients With Secondary Hyperparathyroidism	Phase 2
Completed	`NCT00999037` - FGF-23 (Fibroblast Growth Factor 23) Regulation in Chronic Kidney Disease	N/A
Completed	`NCT00742716` - Safety Study of CTA018 Injection to Treat Stage 5 Chronic Kidney Disease	Phase 2

NCT number	NCT01167309
Study type	Interventional
Source	LEO Pharma
Contact
Status	Completed
Phase	Phase 1
Start date	June 2010
Completion date	December 2011

LEO 27847 - Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Study in Secondary Hyperparathyroidism Patients

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms