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G56W1 in Women With Postmenopausal Osteoporosis

Postmenopausal Osteoporosis Clinical Trial

Official title:
Two-dose, Positive Drug Control, Multicentre, Randomized, Double-blind Study of Recombinant Human Parathyroid Hormone for Injection(rhPTH)(1-34) Once a Week to Treat Postmenopausal Osteoporosis Women for the Evaluation the Pharmacokinetics and Safety and to Explore Therapeutic Effects

Clinical Trial Summary

This study will assess the pharmacokinetics and safety and explore therapeutic effects with once-weekly recombinant human parathyroid hormone for injection ( 1-34 ) ( G56W1 ) in women with post-menopausal osteoporosis .The anticipated time on study treatment is 24 weeks, and the target sample size is 148 individuals.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03720886
Study type Interventional
Source Shenzhen Salubris Pharmaceuticals Co., Ltd.
Contact
Status Active, not recruiting
Phase Phase 1/Phase 2
Start date October 1, 2018
Completion date August 31, 2020
View Details
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