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Phase 1 Completed N=22 Randomized Basic Science

A Study to Estimate the Effect of CYP3A4 Inhibitors (Itraconazole, Diltiazem or Verapamil) on the Pharmacokinetics of Single Dose PF- 00489791 in Healthy Volunteers

Healthy Volunteers
Source: ClinicalTrials.gov NCT02319148 ↗
Enrolled (actual)
22
Serious AEs
0.0%
Results posted
Sep 2016
Primary outcomePrimary: Maximum Observed Plasma Concentration (Cmax) of PF-00489791 — 1140; 1238; 1198; 1186 nanograms per milliliter (ng/mL)

Summary

The primary objective of the study is to estimate the effects of different strong enzyme (CYP3A4) inhibitors, itraconazole, diltiazem, or verapamil on the single dose pharmacokinetics of PF-00489791 in healthy volunteers. The study will enroll approximately 18 subjects that are randomized to 1 of 3 treatment groups. The study is also intended to determine the safety and tolerability of single-dose PF- 00489791 when it is administered with steady-state itraconazole, diltiazem, or verapamil.

Outcome Measures

OutcomeResultp-value
PRIMARY
Maximum Observed Plasma Concentration (Cmax) of PF-00489791
1140; 1238; 1198; 1186
PRIMARY
Area Under the Plasma Concentration-Time Profile From Time 0 Extrapolated to Infinite Time (AUCinf) of PF-00489791
17880; 18140; 16840; 19560
SECONDARY
Area Under the Curve From Time Zero to Last Quantifiable Concentration (AUClast) of PF-00489791
17580; 17980; 16760; 19400
SECONDARY
Time to Reach Maximum Observed Plasma Concentration (Tmax) of PF-00489791
4.00; 3.50; 4.00; 4.00
SECONDARY
Apparent Volume of Distribution (Vz/F) of PF-00489791
18.06; 21.65; 19.98; 19.23
SECONDARY
Apparent Oral Clearance (CL/F) of PF-00489791
18.64; 18.37; 19.81; 17.02
SECONDARY
Terminal Elimination Half-Life (t1/2) of PF-00489791
11.39; 13.85; 11.75; 13.29
SECONDARY
Number of Participants With Laboratory Abnormalities Meeting the Criteria for Potential Clinical Concern
3; 0; 0; 2
SECONDARY
Number of Participants With Potentially Clinically Significant Vital Signs Findings
0; 0; 0; 1; 0; 0
SECONDARY
Number of Participants With Potentially Clinically Significant Electrocardiogram (ECG) Findings
0; 0; 0; 0; 0; 0
SECONDARY
Number of Participants Who Used at Least 1 Concomitant Medication
10; 2; 4; 2; 0; 0
SECONDARY
Number of Participants With Treatment-Emergent Adverse Events (AEs) or Serious Adverse Events (SAEs)
18; 6; 4; 3; 6; 4

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) with a Body Mass Index (BMI) of 17.5 to 30.5 kg/m2; and a total body weight >50 kg (110 lbs.) and with a personally signed and dated informed consent document and who are willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures.
  • Participating female subjects of non-childbearing potential must meet at least one of the following criteria: achieved postmenopausal status; have undergone a documented hysterectomy and/or bilateral oophorectomy; have medically confirmed ovarian failure. All other female subjects (including females with tubal ligations and females that do NOT have a documented hysterectomy, bilateral oophorectomy and/or ovarian failure) will be considered to be of childbearing potential.

Exclusion Criteria

  • Subjects cannot be included in the study if there is: the presence/ history of any disorder that prevents study completion
  • Evidence/history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, or allergic disease
  • Any surgical or medical condition that may interfere with the absorption distribution, metabolism, or excretion of the study drug
  • A positive urine drug screen or history of regular excessive alcohol consumption or use of tobacco-or nicotine-containing products in excess or from 24-hours prior to admission until discharge
  • Treatment with an investigational drug within 30 days (or as determined by the local requirement) or 5 halflives preceding the first dose of study med.
  • Out of range blood pressure including current evidence of orthostatic change in blood pressure
  • Abnormal ECG or history or current evidence of clinically important cardiac conduction abnormalities.
  • Also excluded are: pregnant or breastfeeding female subjects; male subjects with partners currently pregnant; male and female subjects of childbearing potential who are unwilling or unable to use a highly effective method of contraception as described in the protocol for the duration of the study and for at least 28 days after the last dose of investigational product.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02319148). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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