drugset / Trial / NCT01166984

AB103 Peptide Antagonist in Healthy Volunteers

NCT01166984 ↗

Phase 1 Completed 25 enrolled Atox Bio Ltd
RandomizedParallel-groupTriple-blindOther

Summary

The primary objective of this study is to establish the safety profile and maximum tolerated dose (MTD) of AB103 given as a single intravenous (IV) infusion in healthy volunteers.

Timeline

Start
2010-09
Primary completion
2011-06
Completion
2011-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Reltecimod Peptide 7.5 ug/kg Intravenous
Subject Reltecimod Peptide 37.5 ug/kg Intravenous
Subject Reltecimod Peptide 150 ug/kg Intravenous
Subject Reltecimod Peptide 450 ug/kg Intravenous

Indications

No indication recorded.