drugset / Trial / NCT07028320

To Evaluate the Efficacy and Safety of SAL056 for Postmenopausal Women With Osteoporosis at High Fracture Risk

NCT07028320

Phase 3 Completed 493 enrolled Shenzhen Salubris Pharmaceuticals Co., Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

To Evaluate the Efficacy and Safety of SAL056 for Postmenopausal Women with Osteoporosis at High Fracture Risk

Timeline

Start
2021-12-03
Primary completion
2023-12-30
Completion
2024-05-20

Drugs

EvaluationDrugModalityDoseRoute
Comparator Alendronic Acid Small molecule 70 mg Oral
Subject SAL056 Protein / enzyme biologic 56.5 ug Subcutaneous