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Evaluation of Pharmacokinetics, Safety, And Tolerability Of Ertugliflozin (PF-04971729, MK-8835) In Japanese And Western Healthy Participants (MK-8835-041)

Phase 1
Completed
Conditions
Diabetes Mellitus, Type 2
Interventions
Drug: Placebo
Registration Number
NCT01223339
Lead Sponsor
Merck Sharp & Dohme LLC
Brief Summary

This study is to characterize the pharmacokinetics, safety, tolerability, and pharmacodynamics of single and multiple oral doses (SD, MD) of ertugliflozin (PF-04971729, MK-8835) in Japanese healthy participants. The secondary objective is to investigate the safety, tolerability, pharmacokinetics, and pharmacodynamics of single doses of ertugliflozin in Western healthy participants as compared to Japanese healthy participants.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
24
Inclusion Criteria
  • Healthy male and/or female subjects of non-childbearing potential, between the ages of 18 and 55 years, inclusive
  • Body Mass Index (BMI) of 17.5 to 30.5 kg/m2; and a total body weight >50 kg (110 lbs).
  • Japanese subjects must have four Japanese grandparents who were born in Japan.
  • Mean body weight and the body weight range of Western subjects are similar to those of Japanese subjects with a 10% plus and minus error.
  • An informed consent document signed and dated by the subject.
  • Subjects who are willing and able to comply with scheduled visits, treatment plan,laboratory tests, and other study procedures.
Exclusion Criteria
  • Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, or allergic disease
  • Asian or Polynesian subjects in Western subject groups.
  • Any condition possibly affecting drug absorption (eg, gastrectomy).
  • A positive urine drug screen.
  • History of regular alcohol consumption exceeding 7 drinks/week for females or 14 drinks/week for males within 6 months of screening.
  • History or evidence of habitual use of tobacco or nicotine containing products within 3 months of Screening, with the exception of light smoking (up to 5 cigarettes per day or the equivalent).
  • Treatment with an investigational drug within 30 days or 5 half-lives preceding the first dose of study medication.
  • 12-lead ECG demonstrating QTc >450 msec at screening.
  • Subjects with ANY of the following abnormalities on safety laboratory tests):
  • Evidence of glycosuria, as defined by a positive urine dipstick test;
  • Fasting serum triglyceride >300 mg/dL;
  • Fasting LDL-cholesterol > than or equal to 190 mg/dL.
  • Fasting serum glucose >125 mg/dL.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Single Dose Japanese CohortErtugliflozinThis will be a single dose Cohort in which Japanese healthy participants will receive 3 ascending single doses (1 mg, 5 mg, and 25 mg) of ertugliflozin or placebo through 3 dosing periods. A minimum wash out period of 7-days will be set between each dose administration.
Single Dose Japanese CohortPlaceboThis will be a single dose Cohort in which Japanese healthy participants will receive 3 ascending single doses (1 mg, 5 mg, and 25 mg) of ertugliflozin or placebo through 3 dosing periods. A minimum wash out period of 7-days will be set between each dose administration.
Single dose Western cohortErtugliflozinThis will be a single dose Cohort in which Western healthy participants will receive 3 ascending single doses (1 mg, 5 mg, and 25 mg) of ertugliflozin through 3 dosing periods. A minimum wash out period of 7-days will be set between each dose administration.
Multiple Dose Japanese CohortPlaceboThis will be a multiple dose Cohort in which Japanese healthy participants will receive once-daily 25 mg ertugliflozin or placebo for 7 days.
Multiple Dose Japanese CohortErtugliflozinThis will be a multiple dose Cohort in which Japanese healthy participants will receive once-daily 25 mg ertugliflozin or placebo for 7 days.
Primary Outcome Measures
NameTimeMethod
Maximum plasma concentration (Cmax) of ertugliflozin for the Single Dose CohortUp to Day 4 of each treatment period
Urinary Glucose Excretion over 24 hours for the Single Dose CohortUp to 24 hours postdose (Up to Day 2)
Cmax of ertugliflozin for the Multiple Dose CohortUp to Day 10
Tmax of ertugliflozin for the Multiple Dose CohortUp to Day 10
AUClast for ertugliflozin for the Multiple Dose CohortUp to Day 10
AUCinf for ertugliflozin for the Multiple Dose CohortUp to Day 10
t1/2 for the Multiple Dose CohortUp to Day 10
CL/F of ertugliflozin for the Multiple Dose CohortUp to Day 10
Vz/F for the Multiple Dose CohortUp to Day 10
Time taken to reach the maximum observed plasma concentration (Tmax) of ertugliflozin for the Single Dose CohortUp to Day 4 of each treatment period
Area under the plasma concentration-time curve (AUC) from time 0 to time of the last quantifiable concentration (AUClast) for ertugliflozin for the Single Dose CohortUp to Day 4 of each treatment period
AUC from Hour 0 to infinity (AUCinf) for ertugliflozin for the Single Dose CohortUp to Day 4 of each treatment period
Ertugliflozin half life (t1/2) for the Single Dose CohortUp to Day 4 of each treatment period
Apparent clearance (CL/F) of ertugliflozin for the Single Dose CohortUp to Day 4 of each treatment period
Apparent volume of distribution (Vz/F) for the Single Dose CohortUp to Day 4 of each treatment period
Accumulation Ratio of Area Under the Curve for the dosing interval of ertugliflozin (Rac) for the Single Dose CohortUp to Day 4 of each treatment period
Number of participants who experienced an adverse event (AE) for the Single Dose CohortUp to 10 days after the final dose of study drug (Up to Day 11)
Number of participants who discontinued study drug due to an AE for the Single Dose CohortUp to Day 1 of each treatment period
Rac for the Single Dose CohortUp to Day 10
Number of participants who experienced an AE for the Multiple Dose CohortUp to 10 days after the final dose of study drug (Up to Day 17)
Number of participants who discontinued study drug due to an AE for the Multiple Dose CohortUp to Day 7
Urinary Glucose Excretion over 24 hours for the Multiple Dose CohortUp to 24 hours postdose (Up to Day 8)
Secondary Outcome Measures
NameTimeMethod
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