Skip to main content
OpenTrials
Completed

NCT Number: NCT00327808

Inhaled TPI-1020 Versus Inhaled Budesonide in Smokers With Mild Reversible Asthma

The investigators will look at TPI-1020 safety and tolerability in mild to moderate asthmatic smoker subjects.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

McMaster University Hospital, Hamilton, Ontario, Canada

Loading trial locations.

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Males or females 18 through 65 years of age.
  • Smoking history of more than 5 pack/years but less than 25 pack/years and who have no desire to quit smoking despite physician's advice and who currently smoke at least 5 cigarettes per day.
  • Mild to moderate, stable, allergic asthma as defined by American Thoracic Society (ATS) criteria 1
  • History of episodic wheeze and shortness of breath
  • Subjects currently and only receiving inhaled short-acting bronchodilator treatment for asthma.

Exclusion criteria

  • History or symptoms of significant autoimmune, hematological, or neurological disease, including transient ischemic attack (TIA), stroke, seizure disorder, or behavioural disturbances that are judged clinically significant by the Investigator
  • History of serious adverse reaction or hypersensitivity to corticosteroids
  • Abnormal chest X-ray that is judged clinically significant
  • Pregnant or lactating or have positive plasma pregnancy test
  • Use of oral/parenteral/inhaled corticosteroids within the last 28 days or injectable depot corticosteroids within the last 6 weeks.
  • Use of any other asthma-related medications within 1 month of Screening

Treatment and study plan

TPI-1020

Drug

600 mcg BID x 14 days followed by 1200 mcg BID x 7 days

Budesonide

Drug

400 mcg BID x 14 days then 800 mcg/day x 7 more days

Primary outcomes

  1. To determine the safety and tolerability of multiple doses of TPI-1020 in subjects with asthma who smoke

    Time frame: 22 days

Secondary outcomes

  1. To compare sputum neutrophil and eosinophil counts on Day 0 versus Day 15 and Day 22

    Time frame: 22 days

  2. To determine pharmacodynamic effects on forced expiratory volume in 1 second (FEV1) over 8 hours on Day 1 and Day 14

    Time frame: 22 days

  3. To compare pre-dose FEV1 measurements on multiple days throughout the study

    Time frame: 22 days

  4. To compare peak flow measurements throughout the study

    Time frame: 22 days

  5. To compare the use of daily rescue medication (salbutamol) throughout the study

    Time frame: 22 days

  6. To determine the plasma pharmacokinetic (PK) profile on a sub-group of subjects on the first and last day of the dosing period

    Time frame: 22 days

Sponsors and collaborators

Lead sponsor

Syntara

Industry

Registry information

Official study title

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

Important dates

Study start
2006
Primary completion
2007
Study completion
2007
First posted
May 19, 2006
Registry last updated
Dec 3, 2012

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.

Published trials that share one or more normalized conditions with this study.