drugset / Trial / NCT04449939

A Study of Subcutaneous KY1005 in Healthy Volunteers

NCT04449939

Phase 1 Completed 24 enrolled Kymab Limited
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Single centre, open-label, single dose, parallel group study to investigate the PK, safety and tolerability of KY1005 after subcutaneous (s.c.) and intravenous (i.v.) administration, with i.v. KY1005 as a reference treatment.

Timeline

Start
2020-07-07
Primary completion
2020-11-30
Completion
2020-11-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Amlitelimab Monoclonal antibody Subcutaneous