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A Safety Study to Compare the Effect of Two PrEP-001 Nasal Powder Formulations on Nasal Mucosa and Serum Cytokine Production

Upper Respiratory Tract Infections Clinical Trial

Official title:
A Single Centre, Partially Blinded, Randomised Study to Compare the Effect of Two PrEP-001 Nasal Powder Formulations on Nasal Mucosa and Serum Cytokine Production in Healthy Human Volunteers

Clinical Trial Summary

A safety study to compare the effect of two different formulations of PrEP-001 nasal powder when dosed in healthy subjects

Clinical Trial Description

A single centre, randomised, partially blinded placebo-controlled repeat dose study in healthy male subjects to compare the effect of two different formulations of PrEP-001 nasal powder on nasal mucosal and serum cytokine profiles when dosed for up to five days in health subjects and provide additional safety and tolerability information on active PrEP-001 nasal powder. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03198676
Study type Interventional
Source Prep Biopharm Limited
Contact
Status Completed
Phase Phase 1
Start date May 8, 2017
Completion date May 24, 2017
View Details
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