A Study To Evaluate Different Formulations Of PF-06865571 In Healthy Subjects

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 12

Inclusion Criteria

Healthy males and female of non-childbearing potential
Age of 18-55, inclusive
Body Mass Index 17.5 to 30.5 kg/m2, inclusive
Body weight >50 kg
Not on any prescription or non-prescription drugs within 7 days or 5 half-lives prior to first dose.

Exclusion Criteria

Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurological, or allergic disease (including drug allergies, but excluding untreated, asymptomatic, seasonal allergies at the time of dosing).
Any condition possibly affecting drug absorption (eg, gastrectomy).
A positive urine drug test.
History of regular alcohol consumption exceeding 14 drinks/week for female subjects or 21 drinks/week for male subjects (1 drink = 5 ounces [150 mL] of wine or 12 ounces [360 mL] of beer or 1.5 ounces [45 mL] of hard liquor) within 6 months before screening.
Treatment with an investigational drug within 30 days (or as determined by the local requirement) or 5 half lives preceding the first dose of investigational product (whichever is longer).
Screening supine BP >=140 mm Hg (systolic) or >= 90 mm Hg (diastolic), following at least 5 minutes of supine rest.
Screening supine 12 lead ECG demonstrating a corrected QT (QTc) interval >450 msec or a QRS interval >120 msec.
Subjects with ANY of the following abnormalities in clinical laboratory tests at screening, as assessed by the study specific laboratory and confirmed by a single repeat test, if deemed necessary:
- Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) level >=1.25 × upper limit of normal (ULN);
- Total bilirubin level >=1.5 × ULN; subjects with a history of Gilbert's syndrome may have direct bilirubin measured and would be eligible for this study provided the direct bilirubin level is =<ULN.
Fertile male subjects who are unwilling or unable to use a highly effective method of contraception as outlined in this protocol for the duration of the study and for at least 28 days after the last dose of investigational product.
Blood donation (excluding plasma donations) of approximately 1 pint (500 mL) or more within 60 days prior to dosing.
History of sensitivity to heparin or heparin induced thrombocytopenia only if heparin is used to flush any intravenous catheters in the study.
History of human immunodeficiency virus (HIV), hepatitis B, or hepatitis C; positive testing for HIV, hepatitis B surface antigen (HepBsAg), hepatitis B core antibody (HepBcAb), or hepatitis C antibody (HCVAb).
Unwilling or unable to comply with Lifestyle Requirements in the protocol
Subjects who are investigator site staff members directly involved in the conduct of the study and their family members, site staff members otherwise supervised by the investigator, or subjects who are Pfizer employees, including their family members, directly involved in the conduct of the study.
Other acute or chronic medical or psychiatric condition including recent (within the past year) or active suicidal ideation or behavior or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the subject inappropriate for entry into this study.
Subjects who have previously participated in prior studies with PF 06865571 as the investigational product.

Study & Design

Study Type: INTERVENTIONAL

Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
PF-06865571	PF-06865571 Fast release MR tablets	Treatment
PF-06865571	PF-06865571 Immediate release suspension	Treatment
PF-06865571	PF-06865571 Slow release MR tablets	Treatment
PF-06865571	PF-06865571 Immediate release tablets	Treatment

Primary Outcome Measures

Name	Time	Method
Maximum Observed Plasma Concentration (Cmax) for PF-06865571	0,0.5,1,2,3,4,6,8,12,24,36,48 hours post dose in each period
Time to Reach Maximum Observed Concentration for PF-06865571	0,0.5,1,2,3,4,6,8,12,24,36,48 hours post dose in each period	Time to Reach Maximum Observed Plasma Concentration (Tmax)
Area Under the Curve From Time Zero to Last Quantifiable Concentration (AUClast) for PF-06865571	0,0.5,1,2,3,4,6,8,12,24,36,48 hours post dose in each period	Area under the plasma concentration time-curve from zero to the last measured concentration (AUClast)
Area Under the Curve From Time Zero to Extrapolated Infinite Time for PF-06865571	0,0.5,1,2,3,4,6,8,12,24,36,48 hours post dose in each period	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-06865571	0,0.5,1,2,3,4,6,8,12,24,36,48 hours post dose in each period	Plasma Decay Half-Life (t1/2)

Secondary Outcome Measures

Name	Time	Method
Number of subjects with adverse events (AEs)	Baseline up to 35 days after last dose	Number of participants with reported adverse events
Number of subjects with laboratory tests findings of potential clinical importance	Baseline (Day 0) up to 48 hours after last dose of study medication	Number of participants with potentially clinically important laboratory test findings
Number of subjects with electrocardiogram (ECG) findings of potential clinical importance	Baseline (Day 0) up to 48 hours after last dose of study medication	Number of participants with potentially clinically important ECG findings
Number of subjects with vital signs findings of potential clinical importance	Baseline (Day 0) up to 48 hours after last dose of study medication	Number of participants with potentially clinically important vital sign measurements

A Study To Evaluate Different Formulations Of PF-06865571 In Healthy Subjects

Recruitment & Eligibility

Study & Design

Trial Locations

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