drugset / Trial / NCT04512872

A Phase I Study to Evaluate the Safety and Pharmacokinetics of CT-P41 and EU-approved Prolia in Healthy Male Subjects

NCT04512872

Phase 1 Completed 30 enrolled Celltrion
RandomizedParallel-groupQuadruple-blindOther

Summary

This study is a Pilot Phase 1, Double-Blind, Randomized, Two-arm, Parallel group, Single-dose Study to Evaluate the Safety and Pharmacokinetics of CT-P41 and EU-approved Prolia in Healthy Male Subjects

Timeline

Start
2020-10-20
Primary completion
2021-05-04
Completion
2021-05-04

Drugs

EvaluationDrugModalityDoseRoute
Subject CT-P41 Unknown 60 mg Subcutaneous
Comparator Denosumab Monoclonal antibody 60 mg Subcutaneous

Indications

No indication recorded.