TPI-1020
Drug600 mcg BID x 14 days followed by 1200 mcg BID x 7 days
NCT Number: NCT00327808
The investigators will look at TPI-1020 safety and tolerability in mild to moderate asthmatic smoker subjects.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 2
McMaster University Hospital, Hamilton, Ontario, Canada
This study will assess and compare the safety and tolerability of inhaled TPI 1020 versus budesonide. Pharmacokinetic (PK) and pharmacodynamic (PD) parameters will also be studied in a sub-group of subjects.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
600 mcg BID x 14 days followed by 1200 mcg BID x 7 days
400 mcg BID x 14 days then 800 mcg/day x 7 more days
Time frame: 22 days
Time frame: 22 days
Time frame: 22 days
Time frame: 22 days
Time frame: 22 days
Time frame: 22 days
Time frame: 22 days
Syntara
Industry
Multi-Center, Randomized, Double-Blind, Repeated Doses Study to Evaluate the Safety, Tolerability and Pharmacodynamic Activity of Inhaled TPI-1020 Versus Inhaled Budesonide in Smokers With Mild Reversible Asthma
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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