drugset / Trial / NCT05405985

Study to Access the Relative Bioavailability of Subcutaneous Dose of Nemolizumab When Administered Via Auto-Injector Versus Dual-Chamber Syringe

NCT05405985

Phase 1 Completed 192 enrolled Galderma R&D
RandomizedParallel-groupOpen-labelTreatment

Summary

This study was to compare the rate and extent of absorption of a single dose of nemolizumab administered with auto-injectors \[AI\] (test) versus dual-chamber syringes \[DCS\] (reference) under controlled conditions in healthy adult subjects.

Timeline

Start
2022-08-11
Primary completion
2022-11-11
Completion
2022-12-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Nemolizumab Monoclonal antibody 60 mg Subcutaneous

Indications

No indication recorded.