Warming Sensation and Tolerability Study of Acetylcysteine 2% Oral Solution for Productive Cough
Status:
Completed
Trial end date:
2016-03-01
Target enrollment:
Participant gender:
Summary
This is a 1-treatment arm, open label design. This 1-day study includes a screening on day of
attendance at clinic, followed by a washout period of 30 minutes to 8 hours (if participants
are eligible for dosing the same day). The study also includes a supervised dosing with 10 mL
oral solution and a 1 hour in-clinic evaluation period.