drugset / Trial / NCT06504966

Study to Compare the Efficacy, Pharmacokinetics, Pharmacodynamics, Safety, and Immunogenicity of MAB-22 Versus Prolia®

NCT06504966

Phase 3 Withdrawn Xentria, Inc.
RandomizedParallel-groupDouble-blindOther

Summary

Double-blind, Parallel-group, Active-controlled Study to Compare the Efficacy, Pharmacokinetics, Pharmacodynamics, Safety, and Immunogenicity of MAB-22 Versus Prolia®

Timeline

Start
2025-10
Primary completion
2027-10
Completion
2027-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Denosumab Monoclonal antibody 60 mg Subcutaneous
Subject MAB-22 Unknown 60 mg Subcutaneous

Indications