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An Open-Label, Dose-Escalating, Study to Evaluate the Safety, Efficacy and Tolerability of Oral Nadolol for the Treatment of Adults With Mild Asthma
The purpose of this study is to confirm previous observations in asthmatics that chronic nadolol treatment reduces asthmatic airway hyper-responsiveness.
Age
18 - 60 years
Sex
ALL
Healthy Volunteers
No
Baylor College of Medicine
Houston, Texas, United States
Start Date
January 1, 2007
Primary Completion Date
May 1, 2009
Completion Date
June 1, 2009
Last Updated
May 11, 2016
10
ACTUAL participants
nadolol
DRUG
Lead Sponsor
Invion, Inc.
Collaborators
NCT07486401
NCT07219173
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT02327897