drugset / Trial / NCT01533519

A Dose Escalation Study of Intranasal Neuropeptide Y in Post Traumatic Stress Disorder (PTSD)

NCT01533519

Phase 1 Completed 26 enrolled James Murrough
RandomizedCrossoverDouble-blind

Summary

This study is designed to investigate the safety of intranasal administration of NPY using a dose escalation, randomized, double-blinded, placebo-controlled crossover design in a medication-free, symptomatic PTSD group.

Timeline

Start
2012-12
Primary completion
2016-01
Completion
2016-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Neuropeptide Y Peptide 1.4 mg Intranasal
Subject Neuropeptide Y Peptide 2.8 mg Intranasal
Subject Neuropeptide Y Peptide 4.6 mg Intranasal
Subject Neuropeptide Y Peptide 6.8 mg Intranasal
Subject Neuropeptide Y Peptide 9.6 mg Intranasal