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RECRUITING
NCT07062978
PHASE3

A Comparative Study to Valuating the Efficacy and Safety of QL1206 and Prolia®

Sponsor: Qilu Pharmaceutical Co., Ltd.

View on ClinicalTrials.gov

Summary

This study is a multicenter, randomized, double-blind comparative study to valuating the efficacy and safety of QL1206 and Prolia® in postmenopausal women with osteoporosis at high risk of fracture.

Official title: A Multicenter, Randomized, Double-blind Comparative Study to Valuating the Efficacy and Safety of QL1206 and Prolia® in Postmenopausal Women With Osteoporosis at High Risk of Fracture

Key Details

Gender

FEMALE

Age Range

50 Years - 85 Years

Study Type

INTERVENTIONAL

Enrollment

278

Start Date

2025-06-27

Completion Date

2027-01

Last Updated

2025-07-14

Healthy Volunteers

No

Interventions

DRUG

QL1206

QL1206 Denosumab injection(60 mg) was administered subcutaneously once every 6 months for a maximum of 2 consecutive doses throughout the trial.

DRUG

Prolia®

Prolia® Denosumab injection(60 mg) was administered subcutaneously once every 6 months for a maximum of 2 consecutive doses throughout the trial.

Locations (1)

Zhejiang Provincial People's Hospital Bijie Hospital

Guizhou, China