A Study Of The Safety, Tolerability, And Pharmacokinetics Of Multiple Doses Of PF-05180999 In Healthy Adults
Primary Purpose
Migraine
Status
Withdrawn
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Placebo Tablets
PF-05180999 Tablets
Sponsored by
About this trial
This is an interventional basic science trial for Migraine focused on measuring PF-05180999, safety, tolerability, pharmacokinetics, migraine, PDE2, cAMP, cGMP, cantharidin, blister, CYP3A induction
Eligibility Criteria
Inclusion Criteria:
- Healthy male and/or female (of non-childbearing potential) subjects between the ages of 18 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:
- Subjects with Gilbert's disease or screening laboratory test results that deviate from the upper and/or lower limits of the reference or acceptable range. The exception is that all liver function tests must not exceed the upper limit of normal.
- Subjects with evidence of, or history of, hepatic disorder, including acute or chronic hepatitis B or hepatitis C.
- Subjects with very light skin or very dark skin (at the discretion of the investigator).
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
Placebo
PF-05180999
Arm Description
Placebo tablets
Modified-release tablets of PF-05180999
Outcomes
Primary Outcome Measures
Maximum Observed Plasma Concentration (Cmax)
Single dose Cmax
Time to Reach Maximum Observed Plasma Concentration (Tmax)
Single dose Tmax
Area Under the Curve from Time Zero to end of dosing interval (AUCtau)
Single dose AUCtau
Maximum Observed Plasma Concentration at Steady-State (Cmax,ss)
Steady-state Cmax
Time to Reach Maximum Observed Plasma Concentration at Steady-State (Tmax,ss)
Steady-state Tmax
Minimum Observed Plasma Trough Concentration at Steady-State (Cmin,ss)
Steady-state Cmin
Area Under the Curve from Time Zero to End of Dosing Interval at Steady-State (AUCtau,ss)
Steady-state AUCtau
Apparent Oral Clearance (CL/F)
Clearance of a drug is a measure of the rate at which a drug is metabolized or eliminated by normal biological processes. Clearance obtained after oral dose (apparent oral clearance) is influenced by the fraction of the dose absorbed. Drug clearance is a quantitative measure of the rate at which a drug substance is removed from the blood.
Apparent Volume of Distribution (Vz/F)
Volume of distribution is defined as the theoretical volume in which the total amount of drug would need to be uniformly distributed to produce the desired plasma concentration of a drug. Apparent volume of distribution after oral dose (Vz/F) is influenced by the fraction absorbed.
Plasma Decay Half-Life (t1/2)
Plasma decay half-life is the time measured for the plasma concentration to decrease by one half.
Accumulation Ratio (Racc)
Ratio of Day 14 AUCtau to Day 1 AUCtau
Amount Excreted in Urine (Ae)
Amount of drug excreted in urine
Percent of Dose Excreted in Urine (Ae%)
Percent of total dose excreted in urine
Renal Clearance (CLr)
Renal clearance is a quantitative measure of the rate at which a drug substance is removed from the blood via the renal route.
Secondary Outcome Measures
Identification of metabolites of PF-05180999 in urine and plasma
Metabolite identification
Change from Baseline in Total Leukocyte Levels and Leukocyte Subpopulations in Blister Fluid and Blood
Leukocyte levels in blister fluid and blood
Change from Baseline in Cytokine Levels in Blister Fluid
Cytokine levels in blister fluid
Time-Averaged Area Under the Effect Curve (AUEC/t) for Platelet cGMP and cAMP
Time-averaged area under the effect curve
AUEC/t Ratio
Ratio of Day 14 AUEC/t to Day 1 AUEC/t
Urinary 6beta-hydroxycortisol/cortisol ratio
Urinary marker of CYP3A induction
Plasma 4beta-hydroxycholesterol/cholesterol ratio
Plasma marker of CYP3A induction
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01981486
Brief Title
A Study Of The Safety, Tolerability, And Pharmacokinetics Of Multiple Doses Of PF-05180999 In Healthy Adults
Official Title
A Phase I, Placebo Controlled, Randomized, Subject-And Investigator-Blind, Sponsor-Open, Multiple Ascending Dose Study To Evaluate The Safety, Tolerability, And Pharmacokinetics Of PF-05180999 In Healthy Adult Volunteers
Study Type
Interventional
2. Study Status
Record Verification Date
May 2014
Overall Recruitment Status
Withdrawn
Study Start Date
June 2014 (undefined)
Primary Completion Date
January 2015 (Anticipated)
Study Completion Date
January 2015 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Pfizer
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
PF-05180999 is a novel phosphodiesterase-2 (PDE2) inhibitor. The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics of multiple doses of PF-05180999 administered twice daily over 14 days. Exploratory measures of PDE2 inhibition will also be evaluated in blood and blister fluid.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Migraine
Keywords
PF-05180999, safety, tolerability, pharmacokinetics, migraine, PDE2, cAMP, cGMP, cantharidin, blister, CYP3A induction
7. Study Design
Primary Purpose
Basic Science
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo tablets
Arm Title
PF-05180999
Arm Type
Experimental
Arm Description
Modified-release tablets of PF-05180999
Intervention Type
Drug
Intervention Name(s)
Placebo Tablets
Intervention Description
BID modified-release tablets
Intervention Type
Drug
Intervention Name(s)
PF-05180999 Tablets
Intervention Description
BID modified-release tablets (20 to 240 mg BID)
Primary Outcome Measure Information:
Title
Maximum Observed Plasma Concentration (Cmax)
Description
Single dose Cmax
Time Frame
0-12 hours post-dose on Day 1
Title
Time to Reach Maximum Observed Plasma Concentration (Tmax)
Description
Single dose Tmax
Time Frame
0-12 hours post-dose on Day 1
Title
Area Under the Curve from Time Zero to end of dosing interval (AUCtau)
Description
Single dose AUCtau
Time Frame
0-12 hours post-dose on Day 1
Title
Maximum Observed Plasma Concentration at Steady-State (Cmax,ss)
Description
Steady-state Cmax
Time Frame
0-12 hours post-dose on Day 14
Title
Time to Reach Maximum Observed Plasma Concentration at Steady-State (Tmax,ss)
Description
Steady-state Tmax
Time Frame
0-12 hours post-dose on Day 14
Title
Minimum Observed Plasma Trough Concentration at Steady-State (Cmin,ss)
Description
Steady-state Cmin
Time Frame
0-12 hours post-dose on Day 14
Title
Area Under the Curve from Time Zero to End of Dosing Interval at Steady-State (AUCtau,ss)
Description
Steady-state AUCtau
Time Frame
0-12 hours post-dose on Day 14
Title
Apparent Oral Clearance (CL/F)
Description
Clearance of a drug is a measure of the rate at which a drug is metabolized or eliminated by normal biological processes. Clearance obtained after oral dose (apparent oral clearance) is influenced by the fraction of the dose absorbed. Drug clearance is a quantitative measure of the rate at which a drug substance is removed from the blood.
Time Frame
0-48 hours post-final dose on Day 14
Title
Apparent Volume of Distribution (Vz/F)
Description
Volume of distribution is defined as the theoretical volume in which the total amount of drug would need to be uniformly distributed to produce the desired plasma concentration of a drug. Apparent volume of distribution after oral dose (Vz/F) is influenced by the fraction absorbed.
Time Frame
0-48 hours post-final dose on Day 14
Title
Plasma Decay Half-Life (t1/2)
Description
Plasma decay half-life is the time measured for the plasma concentration to decrease by one half.
Time Frame
0-48 hours post-final dose on Day 14
Title
Accumulation Ratio (Racc)
Description
Ratio of Day 14 AUCtau to Day 1 AUCtau
Time Frame
0-12 hours post-dose on Days 1 and 14
Title
Amount Excreted in Urine (Ae)
Description
Amount of drug excreted in urine
Time Frame
0-12 hours post-dose on Day 14
Title
Percent of Dose Excreted in Urine (Ae%)
Description
Percent of total dose excreted in urine
Time Frame
0-12 hours post-dose on Day 14
Title
Renal Clearance (CLr)
Description
Renal clearance is a quantitative measure of the rate at which a drug substance is removed from the blood via the renal route.
Time Frame
0-48 hours post-dose on Day 14
Secondary Outcome Measure Information:
Title
Identification of metabolites of PF-05180999 in urine and plasma
Description
Metabolite identification
Time Frame
0-12 hours post-dose on Day 14
Title
Change from Baseline in Total Leukocyte Levels and Leukocyte Subpopulations in Blister Fluid and Blood
Description
Leukocyte levels in blister fluid and blood
Time Frame
Day 13 and Day 14
Title
Change from Baseline in Cytokine Levels in Blister Fluid
Description
Cytokine levels in blister fluid
Time Frame
Day 13 and Day 14
Title
Time-Averaged Area Under the Effect Curve (AUEC/t) for Platelet cGMP and cAMP
Description
Time-averaged area under the effect curve
Time Frame
0-12 hours post-dose on Day 1 and Day 14
Title
AUEC/t Ratio
Description
Ratio of Day 14 AUEC/t to Day 1 AUEC/t
Time Frame
0-12 hours post-dose on Day 1 and Day 14
Title
Urinary 6beta-hydroxycortisol/cortisol ratio
Description
Urinary marker of CYP3A induction
Time Frame
Day 14
Title
Plasma 4beta-hydroxycholesterol/cholesterol ratio
Description
Plasma marker of CYP3A induction
Time Frame
Day 14
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Healthy male and/or female (of non-childbearing potential) subjects between the ages of 18 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:
Subjects with Gilbert's disease or screening laboratory test results that deviate from the upper and/or lower limits of the reference or acceptable range. The exception is that all liver function tests must not exceed the upper limit of normal.
Subjects with evidence of, or history of, hepatic disorder, including acute or chronic hepatitis B or hepatitis C.
Subjects with very light skin or very dark skin (at the discretion of the investigator).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pfizer CT.gov Call Center
Organizational Affiliation
Pfizer
Official's Role
Study Director
12. IPD Sharing Statement
Links:
URL
https://trialinfoemail.pfizer.com/pages/landing.aspx?StudyID=B3441008&StudyName=A%20Study%20Of%20The%20Safety%2C%20Tolerability%2C%20And%20Pharmacokinetics%20Of%20Multiple%20Doses%20Of%20PF-05180999%20In%20Healthy%20Adults
Description
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A Study Of The Safety, Tolerability, And Pharmacokinetics Of Multiple Doses Of PF-05180999 In Healthy Adults
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