Zhejiang Provincial People's Hospital Bijie Hospital
Guizhou, China
Location status: Recruiting
Location contact
Jun Zhang
CONTACT
NCT Number: NCT07062978
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.
Interested in participating?
Request Info50 year–85 year
Female
Interventional
Phase 3
Guizhou, China
Location status: Recruiting
Jun Zhang
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
QL1206 Denosumab injection(60 mg) was administered subcutaneously once every 6 months for a maximum of 2 consecutive doses throughout the trial.
Prolia® Denosumab injection(60 mg) was administered subcutaneously once every 6 months for a maximum of 2 consecutive doses throughout the trial.
Time frame: Baseline and 12 months
Percent Change From Baseline in lumbar spine(LS)-BMD at Month 12
Contact information is provided by the study sponsor or research team.
Qilu Pharmaceutical Co., Ltd.
Industry
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
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.