Trial Profile

A Twelve-month Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Efficacy and Safety of QL1206 in Chinese Postmenopausal Women With Osteoporosis at High Risk of Fracture

Status: Completed

Phase of Trial: Phase III

Latest Information Update: 14 Feb 2023

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At a glance

01 Feb 2023 Status changed from recruiting to completed, according to Results published in the Acta Pharmacologica Sinica.
01 Feb 2023 Results published in the Acta Pharmacologica Sinica
05 Nov 2019 Planned number of patients changed from 216 to 440.

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