drugset / Trial / NCT02127801

Single Ascending-dose Study of the Efficacy, Safety, Tolerability, and Pharmacokinetics of REGN1908-1909 in Allergic, Adult Participants

NCT02127801 ↗

Phase 1 Completed 74 enrolled Regeneron Pharmaceuticals
RandomizedSingle-groupQuadruple-blindBasic science

Summary

The purposes of this study are to assess the efficacy, safety and tolerability of a single dose of REGN1908-1909 in allergic adult participants, to collect information about how much REGN1908-1909 is in blood over time and to collect information about how the body reacts to REGN1908-1909.

Timeline

Start
2014-10-31
Primary completion
2015-12-31
Completion
2015-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Freneslerbart Monoclonal antibody — —
Subject Mevonlerbart Monoclonal antibody — —

Indications