Safety Profiles, Pharmacokinetics, and Changes in Bone Turnover Markers After Twice‐Weekly Subcutaneous Administration of Teriparatide in Healthy Japanese Postmenopausal Women: A Single‐Blind Randomized Study-Reference-Cited by-同舟云学术

Safety Profiles, Pharmacokinetics, and Changes in Bone Turnover Markers After Twice‐Weekly Subcutaneous Administration of Teriparatide in Healthy Japanese Postmenopausal Women: A Single‐Blind Randomized Study

Published:2019-03-28 Issue:1 Volume:9 Page:87-96
ISSN:2160-763X
Container-title:Clinical Pharmacology in Drug Development
language:en
Short-container-title:Clinical Pharmacology in Drug Development

Author:

Kumagai Yuji¹,Ose Atsushi²,Tanaka Kosuke²,Sugimoto Toshitsugu³

Affiliation:

1. Kitasato University East Hospital Kanagawa Japan

2. Development Planning Clinical Development Center Asahi Kasei Pharma Corporation Tokyo Japan

3. Internal Medicine 1 Shimane University Faculty of Medicine Shimane Japan

Funder

Asahi Kasei Pharma Corporation

Publisher

Wiley

Subject

Pharmacology (medical),Pharmaceutical Science

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cpdd.687

Reference27 articles.

1. Randomized Teriparatide [Human Parathyroid Hormone (PTH) 1–34] Once-Weekly Efficacy Research (TOWER) Trial for Examining the Reduction in New Vertebral Fractures in Subjects with Primary Osteoporosis and High Fracture Risk

2. Pharmacokinetics of teriparatide after subcutaneous administration to volunteers with renal failure: a pilot study

3. Population Pharmacokinetic and Exposure-Response Analysis of Weekly Teriparatide in Osteoporosis Patients

4. Profile of changes in bone turnover markers during once-weekly teriparatide administration for 24 weeks in postmenopausal women with osteoporosis

5. Persistence of and switches from teriparatide treatment among women and men with osteoporosis in the real world: a claims database analysis

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