G56W1 in Women With Postmenopausal Osteoporosis

Status Active, not recruiting

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

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See also
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