drugset / Trial / NCT02163018

HAL-MPE1 First-in-human

NCT02163018 ↗

Phase 1 Completed 17 enrolled HAL Allergy
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Currently, there is no effective causal treatment for peanut allergy. A chemically modified, aluminium hydroxide adsorbed peanut extract (HAL-MPE1) for subcutaneous administration has been developed. Results from in vitro and in vivo preclinical studies demonstrate the immunotherapeutic potential of HAL-MPE1. Therefore, a phase I, single-centre clinical trial has been designed to assess the safety and tolerability of HAL-MPE1 in peanut allergic patients.

Timeline

Start
2014-06
Primary completion
2015-05
Completion
2015-06

Drugs

EvaluationDrugModalityDoseRoute
Subject HAL-MPE1 Unknown — Subcutaneous

Indications