drugset / Trial / NCT03382262

Study to Compare Exposure of TA Following Administration of FX006 or TAcs in Patients With OA of the Shoulder or Hip

NCT03382262

Phase 2 Completed 55 enrolled Pacira Pharmaceuticals, Inc
RandomizedParallel-groupOpen-labelTreatment

Summary

This is an open-label study to compare systemic exposure to triamcinolone acetonide following a dose of extended-release FX006 or immediate-release TAcs (triamcinolone acetonide suspension) in patients with osteoarthritis of the shoulder (glenohumeral joint) or hip

Timeline

Start
2017-12-18
Primary completion
2018-10-09
Completion
2018-10-09

Drugs

EvaluationDrugModalityDoseRoute
Comparator TAcs Unknown 40 mg Other
Subject Tafamidis Unknown 32 mg Other

Indications