drugset / Trial / NCT02604485

A Single-Dose Open-Label Study of XOMA 358 in Subjects With Congenital Hyperinsulinism

NCT02604485 ↗

Phase 2 Completed 10 enrolled XOMA (US) LLC
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and clinical pharmacology of a single dose pharmacokinetics and pharmacodynamics of XOMA 358 in subjects with hypoglycemia associated with congenital hyperinsulinism.

Timeline

Start
2015-10
Primary completion
2017-01
Completion
2017-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Ersodetug Monoclonal antibody — Intravenous