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A Clinical Trial to Evaluate the Safety, Efficacy, and Immunogenicity of DR-5001

2014-08-27 03:42:15 | BioPortfolio

Summary

This is a multicenter, double-blind, randomized, placebo-controlled study to evaluate the safety and efficacy of oral DR-5001 in reducing the attack rate of febrile acute respiratory disease caused by type-4 and type-7 adenovirus as well as determine its immunogenicity.

Description

The study will be conducted at two sites and will include a minimum of 4 visits. The overall study duration for participants will be approximately 8 weeks. Study participants will undergo acute respiratory disease evaluation that will include a throat swab and a blood draw. Each participant will also be contacted in six months for follow-up information.

Study Design

Allocation: Randomized, Control: Placebo Control, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention

Conditions

Respiratory Tract Diseases

Intervention

DR-5001, Placebo

Location

Duramed Investigational Site
Great Lakes
Illinois
United States
60088

Status

Completed

Source

Duramed Research

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:42:15-0400

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Asthma COPD Cystic Fibrosis Pneumonia Pulmonary Medicine Respiratory Respiratory tract infections (RTIs) are any infection of the sinuses, throat, airways or lungs.  They're usually caused by viruses, but they can also ...


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