CKD-841 Pharmacokinetic/Pharmacodynamic Study

Status Completed

Clinical Trial Summary

A randomized, open-label, single dose, parallel design phase I clinical trial to investigate the safety and pharmacokinetic/pharmacodynamics of CKD-841 or Leuplin Inj. 3.75mg after subcutaneous injection in postmenopausal female.

Clinical Trial Description

To investigate the safety and pharmacokinetic/pharmacodynamics of CKD-841 or Leuplinⓡ Inj. 3.75mg after subcutaneous injection in postmenopausal female is the purpose of this trial. ;

Study Design

Related Conditions & MeSH terms

Postmenopausal Disorder

Clinical Trial Details

NCT number	NCT03233932
Study type	Interventional
Source	Chong Kun Dang Pharmaceutical
Contact
Status	Completed
Phase	Phase 1
Start date	April 2016
Completion date	July 2017

View Details

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