drugset / Trial / NCT05976360

A Study to Investigate the Pharmacokinetics, Tolerability and Safety of Two Different Dupilumab Drug Products in Healthy Participants

NCT05976360

Phase 1 Completed 38 enrolled Sanofi Regeneron Pharmaceuticals · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a phase 1, single subcutaneous dose study to evaluate safety and pharmacokinetics of 2 different dupilumab drug product in healthy volunteers. The duration per participant is up to 11 weeks.

Timeline

Start
2014-11-02
Primary completion
2015-01-17
Completion
2015-01-17

Drugs

EvaluationDrugModalityDoseRoute
Subject Dupilumab Monoclonal antibody Subcutaneous

Indications

No indication recorded.