Expired Study
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San Diego, California 92130


Purpose:

This is a phase one study to evaluate the safety, tolerability, and bioavailability of nebulized AIR645.


Criteria:

Inclusion Criteria*: - Good General Health (with or without allergic rhinitis and/or controlled asthma) - Non-smoker for at least 2 years - Normal lung function (DLCO) - Able to provide informed consent and to understand and comply with the requirements of the study Exclusion Criteria*: - Clinically significant medical history or condition which precludes participation - Clinically significant ECG abnormality - Clinically significant VS or PE abnormality - Clinically significant screening lab abnormality - Abnormal lung function (FEV1 <80% predicted) - Respiratory infection within 14 days of randomization - HBV, HCV, or HIV - Breastfeeding or pregnant female - History of alcohol abuse or illicit drug use within past 24 months - Use of any tobacco or nicotine-containing product within past 6 months - Use of any herbal supplement, over-the-counter drug, or prescription drug that is not allowed per protocol - Use of any investigational drug within past 30 days - Use of any investigational monoclonal antibody or recombinant protein within past 90 days - Donation of plasma within past 7 days - Donation or loss of whole blood within past 56 days - Simplified list of I/E criteria; unabridged list available upon request.


NCT ID:

NCT00658749


Primary Contact:

Study Director
Mike Hodges, MD
Altair Therapeutics


Backup Contact:

N/A


Location Contact:

San Diego, California 92130
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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