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Study to Evaluate the Pharmacokinetics (PK), Pharmacodynamics (PD), and Usability of Abaloparatide-solid Microstructured Transdermal System (sMTS) in Postmenopausal Women With Low Bone Mineral Density (BMD)

Postmenopausal Osteoporosis Clinical Trial

Official title:
A Prospective, Single Arm Study to Evaluate the Pharmacokinetics, Pharmacodynamics, and Usability of Abaloparatide-sMTS in Postmenopausal Women With Low Bone Mineral Density

Clinical Trial Summary

This was an open-label, single-center study to evaluate the usability of abaloparatide-sMTS by participants with low BMD.

Clinical Trial Description

This study aimed to evaluate the ability of participants to self-administer 300 μg abaloparatide-sMTS over a period of 29 days based on PK and PD markers. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04366726
Study type Interventional
Source Radius Health, Inc.
Contact
Status Completed
Phase Phase 1
Start date April 9, 2019
Completion date May 14, 2019
View Details
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