Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06898060

To Evaluate the Efficacy and Safety of Abaloparatide Injection (QLG2128) in the Treatment of Postmenopausal Women With Osteoporosis and at High Risk of Fracture

A Multicenter, Randomized, Open-label, Parallel Controlled, Phase III Clinical Study to Evaluate the Efficacy and Safety of Abaloparatide Injection (QLG2128) in the Treatment of Postmenopausal Women With Osteoporosis and at High Risk of Fracture

Status
Not Yet Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
282 (estimated)
Sponsor
Qilu Pharmaceutical Co., Ltd. · Industry
Sex
All
Age
50 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the efficacy and safety of QLG2128 in the treatment of postmenopausal women with osteoporosis and at high risk of fracture.

Conditions

Interventions

TypeNameDescription
DRUGQLG2128Recommended dosage is 80 μg subcutaneously once daily,52week
DRUGTeriparatide InjectionRecommended dosage is 20μg subcutaneously once daily,52week

Timeline

Start date
2025-06-01
Primary completion
2027-05-01
Completion
2027-05-01
First posted
2025-03-27
Last updated
2025-03-27

Source: ClinicalTrials.gov record NCT06898060. Inclusion in this directory is not an endorsement.