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Clinical Trials/NCT02151617
NCT02151617
Completed
Phase 1

A Phase 1 Double Blind (3rd Party Open) Randomized, Placebo Controlled, Dose Escalation Study To Investigate The Safety,Tolerability, Pharmacokinetics And Pharmacodynamics Of Repeat Doses Of Pf-06743649 With Or Without Food In Healthy Adult Subjects

Pfizer1 site in 1 country40 target enrollmentJune 2014

Overview

Phase
Phase 1
Intervention
Placebo
Conditions
Healthy
Sponsor
Pfizer
Enrollment
40
Locations
1
Primary Endpoint
Maximum Observed Plasma Concentration (Cmax)
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The purpose of this study in healthy people is to evaluate safety, toleration and time course of plasma concentration of multiple oral doses of PF-06743649. The pharmacodynamic activity of PF-06743649 will also be assessed. The effect of food on PK of PF-06743649 will also be investigated.

Registry
clinicaltrials.gov
Start Date
June 2014
End Date
December 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Pfizer
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Healthy male and/or female subjects between the ages of 18 and 55 years, inclusive. (Healthy is defined as no clinically relevant abnormalities identified by a detailed medical history, full physical examination, including blood pressure and pulse rate measurement, 12-lead ECG and clinical laboratory tests).
  • Body Mass Index (BMI) of 17.5 to 30.5 kg/m2; and a total body weight \>50 kg (110 lbs).
  • Evidence of a personally signed and dated informed consent document indicating that the subject (or a legally acceptable representative) has been informed of all pertinent aspects of the study.

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).
  • Any condition possibly affecting drug absorption (eg, gastrectomy).
  • Evidence of gout/hyperuricemia, measured sUA \>8 mg/dL at screening.
  • Experienced an episode of nephrolithiasis or ureterolithiasis.

Arms & Interventions

Cohort 5-PF-06743649 or placebo

Intervention: Placebo

Cohort 1-PF-06743649 or placebo

Subjects will be randomized to receive PF-06743649 or placebo as 2 single doses in periods 1 and 2 either in the fed or fasted state followed by once daily dosing for 14 days in period 3

Intervention: PF-06743649

Cohort 1-PF-06743649 or placebo

Subjects will be randomized to receive PF-06743649 or placebo as 2 single doses in periods 1 and 2 either in the fed or fasted state followed by once daily dosing for 14 days in period 3

Intervention: Placebo

Cohort 2-PF-06743649 or placebo

Intervention: PF-06743649

Cohort 2-PF-06743649 or placebo

Intervention: Placebo

Cohort 3-PF-06743649 or placebo

Intervention: PF-06743649

Cohort 3-PF-06743649 or placebo

Intervention: Placebo

Cohort 4-PF-06743649 or placebo

Intervention: PF-06743649

Cohort 4-PF-06743649 or placebo

Intervention: Placebo

Cohort 5-PF-06743649 or placebo

Intervention: PF-06743649

Outcomes

Primary Outcomes

Maximum Observed Plasma Concentration (Cmax)

Time Frame: up to 14 days

Time to Reach Maximum Observed Plasma Concentration (Tmax)

Time Frame: up to 14 days

Plasma Decay Half-Life (t1/2)

Time Frame: up to 14 days

Amount of drug recovered unchanged in urine during the dosing interval (Aetau)

Time Frame: up to 14 days

Area Under the Curve from Time Zero to end of dosing interval (AUCtau)

Time Frame: up to 14 days

Renal clearance (CLr)

Time Frame: up to 14 days

Percent of dose recovered unchanged in urine during the dosing interval(Aetau%)

Time Frame: up to 14 days

Secondary Outcomes

  • Change from baseline in serum uric acid level(up to 14 days)
  • Urinary hypoxanthine levels(up to 14 days)
  • Change from baseline in serum levels of xanthine and hypoxanthine(up to 14 days)
  • Urinary uric acid levels(up to 14 days)
  • Urinary xanthine levels(up to 14 days)

Study Sites (1)

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