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Clinical Trial Summary

The purpose of this research study is to learn how effective and safe FP01 lozenges are when given to subjects with a cough due to an upper respiratory tract infection. The study will include subjects who have an upper respiratory tract infection, with a cough of less than six weeks duration.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01597349
Study type Interventional
Source Cerecor Inc
Contact
Status Completed
Phase Phase 2
Start date May 2012
Completion date September 2012

See also
  Status Clinical Trial Phase
Completed NCT00547846 - A Phase II Clinical Study of PDC-748 in Patients With Acute Cough Phase 2
Terminated NCT03569033 - Study of Gefapixant (MK-7264) in Acute Cough for Participants With Induced Viral Upper Respiratory Tract Infection (URTI) (MK-7264-013) Phase 2
Completed NCT02396706 - RCT to Evaluate the Efficacy and Safety of Ivy Leaves Cough Liquid vs. Placebo in the Treatment of Acute Cough Phase 2