drugset / Trial / NCT02045472

A Study of VIS410 to Assess Safety and Pharmacokinetics

NCT02045472 ↗

Phase 1 Completed 41 enrolled Visterra, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess the safety, tolerability, immunogenicity and pharmacokinetics of single escalating doses of VIS410 in healthy volunteers.

Timeline

Start
2014-09
Primary completion
2015-05
Completion
2015-05

Drugs

EvaluationDrugModalityDoseRoute
Subject VIS410 Monoclonal antibody 2 mg/kg —
Subject VIS410 Monoclonal antibody 50 mg/kg —

Indications