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An Efficacy and Safety Study of Theraflu Day Powder as Oral Solution for Cold and Flu

Infections, Respiratory Tract Clinical Trial

Official title:
An Open-label, Multicenter, Randomized, Parallel Group, Single-dose Study to Assess the Short Term Efficacy and Safety of Paracetamol 500 mg + Phenylephrine HCl 10 mg + Vitamin C 200 mg Powder for Oral Solution in Subjects With Symptoms of an Upper Respiratory Tract Infection

Clinical Trial Summary

The purpose of the study is to assess the short term efficacy of the Theraflu Aktiv powder for oral solution in the Russian population as compared to an untreated group to support the indication of "Short term relief of the symptoms of colds, chills and influenza, including mild to moderate pain, fever and nasal congestion".

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02678234
Study type Interventional
Source GlaxoSmithKline
Contact
Status Withdrawn
Phase Phase 3
Start date February 1, 2017
Completion date April 1, 2017
View Details
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