Back to resultsA Study To Estimate The Time Course Of PF-00241939 Concentration In The Blood After Dosing With Oral Inhalation From Dry Powder Inhalers
Primary Purpose
Pharmacokinetics
Status
Completed
Phase
Phase 1
Locations
Singapore
Study Type
Interventional
Intervention
Treatment A
Treatment B
Treatment C
Treatment D
Treatment E
Treatment F
Treatment G
Sponsored by
About this trial
This is an interventional basic science trial for Pharmacokinetics
Eligibility Criteria
Inclusion Criteria:
- Healthy male and/or female subjects between the ages of 21 and 55 years.
- Body Mass Index (BMI) of 17.5 to 30.5 kg/m2; and a total body weight >50 kg (110 lbs).
Exclusion Criteria:
- Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, or allergic disease (including drug allergies, but excluding untreated, asymptomatic, seasonal allergies at time of dosing).
- Pregnant or nursing females.
- A positive urine drug screen.
Sites / Locations
- Pfizer Investigational Site
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm 6
Arm 7
Arm Type
Experimental
Experimental
Experimental
Active Comparator
Active Comparator
Active Comparator
Active Comparator
Arm Label
Treatment A
Treatment B
Treatment C
Treatment D
Treatment E
Treatment F
Treatment G
Arm Description
Outcomes
Primary Outcome Measures
Plasma pharmacokinetic parameters: AUClast and Cmax.
Secondary Outcome Measures
Plasma pharmacokinetic parameters: AUC24, AUCinf, Tmax and half-life.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01181700
Brief Title
A Study To Estimate The Time Course Of PF-00241939 Concentration In The Blood After Dosing With Oral Inhalation From Dry Powder Inhalers
Official Title
An Open Study To Estimate The Plasma Pharmacokinetics Of PF-00241939 Administered Via Oral Inhalation Using Dry Powder Inhalers
Study Type
Interventional
2. Study Status
Record Verification Date
January 2011
Overall Recruitment Status
Completed
Study Start Date
October 2010 (undefined)
Primary Completion Date
January 2011 (Actual)
Study Completion Date
January 2011 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Pfizer
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to investigate the time course of PF-00241939 concentrations in the blood following dosing by oral inhalation using dry powder inhalers.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pharmacokinetics
7. Study Design
Primary Purpose
Basic Science
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
42 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Treatment A
Arm Type
Experimental
Arm Title
Treatment B
Arm Type
Experimental
Arm Title
Treatment C
Arm Type
Experimental
Arm Title
Treatment D
Arm Type
Active Comparator
Arm Title
Treatment E
Arm Type
Active Comparator
Arm Title
Treatment F
Arm Type
Active Comparator
Arm Title
Treatment G
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Treatment A
Intervention Description
PF-00241939 300 ug using inhaler A
Intervention Type
Drug
Intervention Name(s)
Treatment B
Intervention Description
PF-00241939 300 ug using inhaler A
Intervention Type
Drug
Intervention Name(s)
Treatment C
Intervention Description
PF-00241939 300 ug using inhaler A
Intervention Type
Drug
Intervention Name(s)
Treatment D
Intervention Description
PF-00241939 300 ug using inhaler B
Intervention Type
Drug
Intervention Name(s)
Treatment E
Intervention Description
PF-00241939 300 ug using inhaler B
Intervention Type
Drug
Intervention Name(s)
Treatment F
Intervention Description
PF-00241939 300 ug using inhaler B
Intervention Type
Drug
Intervention Name(s)
Treatment G
Intervention Description
PF-00241939 300 ug using inhaler B
Primary Outcome Measure Information:
Title
Plasma pharmacokinetic parameters: AUClast and Cmax.
Time Frame
36 hours
Secondary Outcome Measure Information:
Title
Plasma pharmacokinetic parameters: AUC24, AUCinf, Tmax and half-life.
Time Frame
36 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Healthy male and/or female subjects between the ages of 21 and 55 years.
Body Mass Index (BMI) of 17.5 to 30.5 kg/m2; and a total body weight >50 kg (110 lbs).
Exclusion Criteria:
Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, or allergic disease (including drug allergies, but excluding untreated, asymptomatic, seasonal allergies at time of dosing).
Pregnant or nursing females.
A positive urine drug screen.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pfizer CT.gov Call Center
Organizational Affiliation
Pfizer
Official's Role
Study Director
Facility Information:
Facility Name
Pfizer Investigational Site
City
Singapore
ZIP/Postal Code
188770
Country
Singapore
12. IPD Sharing Statement
Links:
URL
https://trialinfoemail.pfizer.com/pages/landing.aspx?StudyID=B0871015&StudyName=A%20Study%20To%20Estimate%20The%20Time%20Course%20Of%20PF-00241939%20Concentration%20In%20The%20Blood%20After%20Dosing%20With%20Oral%20Inhalation%20From%20Dry%20Powder%20Inha
Description
To obtain contact information for a study center near you, click here.
Learn more about this trial
A Study To Estimate The Time Course Of PF-00241939 Concentration In The Blood After Dosing With Oral Inhalation From Dry Powder Inhalers
We'll reach out to this number within 24 hrs