drugset / Trial / NCT01224717

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Oral Doses of PTH134 in Post-menopausal Women

NCT01224717

Phase 1 Completed 104 enrolled Novartis
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is designed to provide information about the bone-anabolic response of PTH134 when administered orally, in comparison to Forsteo®, the sub-cutaneous form of teriparatide, the active ingredient in PTH134.

Timeline

Start
2010-09
Primary completion
2011-04
Completion

Drugs

EvaluationDrugModalityDoseRoute
Comparator Teriparatide Protein / enzyme biologic Oral
Comparator Teriparatide Protein / enzyme biologic Subcutaneous