drugset / Trial / NCT00936650

A Study to Assess the Efficacy and Safety of Twice-Daily Dose Regimens of an Oral Calcimimetic Agent AMG 073 (Cinacalcet) in Primary Hyperparathyroidism (PHPT)

NCT00936650

Phase 2 Completed 78 enrolled Amgen
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This randomized, placebo-controlled study in patients with primary HPT was designed to evaluate the efficacy, safety, pharmacokinetics, and health-related quality of life (HRQOL) of AMG 073 when administered 2 times a day (BID). The study consisted of 3 phases: a 12-week dose-titration phase, a 12-week maintenance phase, and a 28-week follow-up phase.

Timeline

Start
1999-11
Primary completion
2001-03
Completion
2001-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Cinacalcet Other / unclassified 30 mg Oral
Subject Cinacalcet Other / unclassified 40 mg Oral
Subject Cinacalcet Other / unclassified 50 mg Oral