drugset / Trial / NCT02426021

Phase 1 Single Subcutaneous Dose Study of MLN1202

NCT02426021

Phase 1 Withdrawn Takeda
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The objective of the study is to investigate the safety, pharmacokinetics, and pharmacodynamic effect of a single dose of MLN1202 in healthy Japanese male adults.

Timeline

Start
2015-04
Primary completion
2015-11
Completion
2015-11

Drugs

EvaluationDrugModalityDoseRoute
Subject PLOZALIZUMAB Monoclonal antibody 75 mg Subcutaneous
Subject PLOZALIZUMAB Monoclonal antibody 105 mg Subcutaneous
Subject PLOZALIZUMAB Monoclonal antibody 150 mg Subcutaneous
Subject PLOZALIZUMAB Monoclonal antibody 450 mg Subcutaneous

Indications

No indication recorded.