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Topical Multiple Ascending Dose Study for PF-06423264

Phase 1
Terminated
Conditions
Normal Healthy
Interventions
Other: Placebo
Registration Number
NCT02778477
Lead Sponsor
Pfizer
Brief Summary

The current study is the first clinical trial proposed with PF-06423264. It is designed to evaluate the safety, tolerability, and pharmacokinetics (PK) following administration of multiple ascending doses of PF-06423264 to healthy adult subjects with or without oily skin.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
65
Inclusion Criteria
  • Healthy males and female of non-childbearing potential;
  • Body Mass Index 17.5-35.5 kg/m2;
  • Body weight >50 kg;
Exclusion Criteria
  • Evidence of history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, or allergic disease (including drug allergises, but excluding untreated, asymptomatic, seasonal allergies at time of dosing)

Study & Design

Study Type
INTERVENTIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Part A_Cohort 6_PlaceboPlaceboMultiple dose of placebo
Part A_Cohort 2_ActivePF-06423264Multiple ascending dose of PF-06423264
Part A_Cohort 3_PlaceboPlaceboMultiple dose of placebo
Part B_Cohort 1_PlaceboPlaceboMultiple doses of placebo
Part A_Cohort 1_PlaceboPlaceboMultiple dose of placebo
Part A_Cohort 3_ActivePF-06423264Multiple ascending dose of PF-06423264
Part A_Cohort 5_ActivePF-06423264Multiple ascending dose of PF-06423264
Part A_Cohort 2_PlaceboPlaceboMultiple dose of placebo
Part A_Cohort 4_PlaceboPlaceboMultiple dose of placebo
Part A_Cohort 5_PlaceboPlaceboMultiple dose of placebo
Part A_Cohort 6_ActivePF-06423264Multiple ascending dose of PF-06423264
Part B_Cohort 2_ActivePF-06423264Multiple doses of PF-06423264
Part A_Cohort 1_ActivePF-06423264Multiple ascending dose of PF-06423264
Part A_Cohort 4_ActivePF-06423264Multiple ascending dose of PF-06423264
Part B_Cohort 2_PlaceboPlaceboMultiple doses of placebo
Part A_Cohort 7_ActivePF-06423264Multiple ascending dose of PF-06423264
Part A_Cohort 7_PlaceboPlaceboMultiple ascending dose of placebo
Part B_Cohort 1_ActivePF-06423264Multiple doses of PF-06423264
Primary Outcome Measures
NameTimeMethod
Number of Participants With Abnormal Electrocardiogram (ECG)Baseline (Day 0) up to 28 days after last dose

Criteria for potential clinical concern in ECG parameters: Maximum QTcF interval (Fridericia's Correction) in range of 450 to less than 480 msec, maximum QTc interval increase from baseline in range of 30 to less than 60 msec and \>=60 msec.

Number of Participants With Categorical Vital Signs DataBaseline (Day 0) up to 28 days after last dose

Number of participants with maximum increase from Baseline in sitting SBP and DBP of greater than or equal to 30 mmHg was reported.

Number of Participants With Clinical Laboratory AbnormalitiesBaseline (Day 0) up to 28 days after last dose

Following parameters were analyzed for laboratory examination: hematology (hemoglobin, hematocrit, red blood cell count, platelet count, white blood cell count, total neutrophils, eosinophils, monocytes, basophils, lymphocytes); liver function (aspartate aminotransferase, alanine aminotransferase, total bilirubin, lactate dehydrogenase, alkaline phosphatase, albumin, total protein); renal function (blood urea nitrogen, creatinine, uric acid); electrolytes (sodium, potassium, chloride, calcium, phosphate, bicarbonate); clinical chemistry (glucose, creatine kinase); immunology (CRP); urinalysis (dipstick \[urine specific gravity, decimal logarithm of reciprocal of hydrogen ion activity {pH} of urine, glucose, protein, blood, ketones, bilirubin\], microscopy \[urine RBC, WBC, urate crystals, calcium, oxalate, miscellaneous \[urine mucus and leucocytes\]).

Number of Subjects With Treatment Emergent Treatment-Related Adverse Events (AEs) or other safety concernsBaseline (Day 0) up to 28 days after last dose of study medication

Assessment by adverse event monitoring, 12 lead ECGs, telemetry, vital signs and clinical safety laboratory measurements.

Treatment-related AE was any untoward medical occurrence attributed to study drug in a subject who received study drug. Serious adverse event (SAE) was an AE resulting in any of the following outcomes or deemed significant for any other reason: death; initial or prolonged inpatient hospitalization; life-threatening experience (immediate risk of dying); persistent or significant disability/incapacity; congenital anomaly. Treatment-emergent are events between first dose of study drug and up to 28 days after last dose that were absent before treatment or that worsened relative to pretreatment state. Relatedness to Drug was assessed by the investigator (Yes/No). Subjects with multiple occurrences of an AE within a category were counted once within the category.

Number of Participants with Draize-like scoring and clinical observationBaseline (Day 1) up to Day 42+3

Modified Draize-like scoring and clinical observation. Severity estimated by clinical signs and scoring; ranged 0-4: 0= No reaction visible, 1= Trace reaction - barely perceptible pinkness, 2= Mild reaction - readily visible pinkness, 3= Moderate reaction - definite redness, 4= Strong to severe reaction - very intense redness.

Secondary Outcome Measures
NameTimeMethod
Area Under the Curve From Time Zero to End of Dosing Interval (AUCtau) for PF-064232640, 0.5, 1, 2, 4, 5, 6, 8, 12, 24 hours post dose on Day 1 and 0, 0.5, 1, 2, 4, 5, 6, 8, 12, 24, 36, and 48 hours post dose on Day 14

Area under the concentration curve from time 0 to end of dosing interval (AUCtau), where dosing interval was 12 hours.

Plasma Decay Half-Life (t1/2) for PF-064232640, 0.5, 1, 2, 4, 5, 6, 8, 12, 24 hours post dose on Day 1 and 0, 0.5, 1, 2, 4, 5, 6, 8, 12, 24, 36, and 48 hours post dose on Day 14

Plasma Decay Half-Life (t1/2)

change from baseline in sebum lipid components and sebum excretionBaseline (Day 0) up to 16 days after last dose of study medication

change from baseline in sebum lipid components and sebum excretion as assessed with Sebutape strips and Sebumeter measurements on the forehead of subjects with oily skin

Maximum Observed Plasma Concentration (Cmax) for PF-064232640, 0.5, 1, 2, 4, 5, 6, 8, 12, 24 hours post dose on Day 1 and 0, 0.5, 1, 2, 4, 5, 6, 8, 12, 24, 36, and 48 hours post dose on Day 14

Maximum Observed Plasma Concentration (Cmax)

Time to Reach Maximum Observed Concentration for PF-064232640, 0.5, 1, 2, 4, 5, 6, 8, 12, 24 hours post dose on Day 1 and 0, 0.5, 1, 2, 4, 5, 6, 8, 12, 24, 36, and 48 hours post dose on Day 14

Time to Reach Maximum Observed Plasma Concentration (Tmax)

Apparent Total Body Clearance (CL/F) for0, 0.5, 1, 2, 4, 5, 6, 8, 12, 24 hours post dose on Day 1 and 0, 0.5, 1, 2, 4, 5, 6, 8, 12, 24, 36, and 48 hours post dose on Day 14

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 apparent total body clearance is influenced by the fraction of the dose absorbed. Clearance was estimated from population pharmacokinetic (PK) modeling. Drug clearance is a quantitative measure of the rate at which a drug substance is removed from the blood.

Observed Accumulation Ratio (Rac) for PF-064232640, 0.5, 1, 2, 4, 5, 6, 8, 12, 24 hours post dose on Day 1 and 0, 0.5, 1, 2, 4, 5, 6, 8, 12, 24, 36, and 48 hours post dose on Day 14

Rac was calculated as, area under the curve from time zero to end of dosing interval on Day Y (AUCtau) divided by area under the curve from time zero to end of dosing interval on Day X(AUCtau).

Apparent Volume of Distribution (Vz/F) for PF-064232640, 0.5, 1, 2, 4, 5, 6, 8, 12, 24 hours post dose on Day 1 and 0, 0.5, 1, 2, 4, 5, 6, 8, 12, 24, 36, and 48 hours post dose on Day 14

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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