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A Single Oral Dose Study Of PF-06409577 In Healthy Adult Subjects

Phase 1
Terminated
Conditions
Healthy
Interventions
Drug: PF-06409577 or Placebo
Registration Number
NCT02286882
Lead Sponsor
Pfizer
Brief Summary

PF-06409577 is a new compound proposed for the treatment of diabetic nephropathy. The primary purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics of single oral doses of PF-06409577 in healthy adult subjects.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
39
Inclusion Criteria
  • Healthy male, or female subjects of non childbearing potential.
  • Body Mass Index (BMI) of 18 to 30.5 kg/m2; and a total body weight >50 kg
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)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Cohort 3: PF-06409577 or placeboPF-06409577 or PlaceboSingle ascending doses of PF-06409577 or placebo to investigate the safety, tolerability, and PK.
Cohort 1: PF-06409577 or placeboPF-06409577 or PlaceboSingle ascending doses of PF-06409577 or placebo to investigate the safety, tolerability, and PK.
Cohort 5: PF-06409577 or placeboPF-06409577 or PlaceboSingle ascending doses of PF-06409577 or placebo to investigate the safety, tolerability, and PK.
Cohort 2: PF-06409577 or placeboPF-06409577 or PlaceboSingle ascending doses of PF-06409577 or placebo to investigate the safety, tolerability, and PK.
Cohort 7: PF-06409577 or placeboPF-06409577 or PlaceboSingle ascending doses of PF-06409577 or placebo to investigate the safety, tolerability, and PK.
Cohort 8: PF-06409577 or placeboPF-06409577 or PlaceboSingle ascending doses of PF-06409577 or placebo to investigate the safety, tolerability, and PK.
Cohort 4: PF-06409577 or placeboPF-06409577 or PlaceboSingle ascending doses of PF-06409577 or placebo to investigate the safety, tolerability, and PK.
Cohort 6: PF-06409577 or placeboPF-06409577 or PlaceboSingle ascending doses of PF-06409577 or placebo to investigate the safety, tolerability, and PK.
Cohort 9: PF-06409577 or placeboPF-06409577 or PlaceboSingle ascending doses of PF-06409577 or placebo to investigate the safety, tolerability, and PK.
Primary Outcome Measures
NameTimeMethod
Number of Participants With Adverse Events (AEs)0-48 hours post dose
Number of Participants With Electrocardiogram (ECG) Findings of Potential Clinical Importance0-48 hours post dose
Number of Participants With Laboratory Test Values of Potential Clinical Importance0-48 hours post dose
Number of Participants With Vital Signs Findings (Including Bood Pressure and Pulse Rate) of Potential Clinical Importance0-48 hours post dose
Number of Participants With Echocardiogram Findings of Potential Clinical Importance0-48 hours post dose
Secondary Outcome Measures
NameTimeMethod
Area Under the Curve From Time Zero to Extrapolated Infinite Time [AUC (0 - infinity)] for PF-064095770, 0.5, 1, 2, 3, 4, 6, 8, 12, 16, 24, 36, 48 hours post dose

AUC (0 - infinity)= Area under the plasma concentration versus time curve (AUC) from time zero (pre-dose) to extrapolated infinite time (0 - infinity). It is obtained from AUC (0 - t) plus AUC (t - infinity).

Plasma Decay Half-Life (t1/2) for PF-064095770, 0.5, 1, 2, 3, 4, 6, 8, 12, 16, 24, 36, 48 hours post dose

Plasma Decay Half-Life (t1/2)

Apparent Oral Clearance (CL/F) for PF-064095770, 0.5, 1, 2, 3, 4, 6, 8, 12, 16, 24, 36, 48 hours post dose

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.

Total amount of PF-06409577 excreted in the urine over 24 hours, expressed as percent of dose (%Ae24)0-24 hours post dose

Total amount of unchanged drug excreted in the urine over 24 hours, expressed as percent of dose.

Area Under the Curve From Time Zero to Last Quantifiable Concentration (AUClast) for PF-064095770, 0.5, 1, 2, 3, 4, 6, 8, 12, 16, 24, 36, 48 hours post dose

Area under the plasma concentration time-curve from zero to the last measured concentration (AUClast)

Renal clearance for PF-064095770-24 hours post dose

Renal clearance of a drug is a measure of the rate at which a drug is excreted unchanged into urine.

Area Under the Curve From Time Zero to Time 24 hours (AUC24) for PF-064095770, 0.5, 1, 2, 3, 4, 6, 8, 12, 16, 24 hours post dose

Area under the plasma concentration time-curve from zero to time 24 hours post dose (AUC24)

Time to Reach Maximum Observed Plasma Concentration (Tmax) for PF-064095770, 0.5, 1, 2, 3, 4, 6, 8, 12, 16, 24, 36, 48 hours post dose

Time to Reach Maximum Observed Plasma Concentration (Tmax)

Total amount of PF-06409577 excreted in the urine over 24 hours (Ae24)0-24 hours post dose

Total amount of unchanged drug excreted in the urine over 24 hours.

Maximum Observed Plasma Concentration (Cmax) for PF-064095770, 0.5, 1, 2, 3, 4, 6, 8, 12, 16, 24, 36, 48 hours post dose

Maximum Observed Plasma Concentration (Cmax)

Apparent Volume of Distribution (Vz/F) for PF-064095770, 0.5, 1, 2, 3, 4, 6, 8, 12, 16, 24, 36, 48 hours post dose

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.

Trial Locations

Locations (1)

Pfizer Clinical Research Unit

🇧🇪

Brussels, Belgium

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