drugset / Trial / NCT01533519
A Dose Escalation Study of Intranasal Neuropeptide Y in Post Traumatic Stress Disorder (PTSD)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |