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Phase 1 Completed N=24

A Study of the Effect of Multiple Doses of Rifampin on the Single Dose Pharmacokinetics of RO5424802

Healthy Volunteer
Source: ClinicalTrials.gov NCT01940510 ↗
Enrolled (actual)
24
Serious AEs
0.0%
Results posted
Oct 2016
Primary outcomePrimary: Area Under the Plasma Concentration-Time Curve From Time Zero to Extrapolated Infinite Time (AUC[0-inf]) of Alectinib — 3990; 1020 ng*hour/mL

Summary

This single center, open-label, 3-period, fixed-sequence study will evaluate the effect of multiple oral doses of rifampin on the pharmacokinetics of a single oral dose of RO5424802 in healthy volunteers. Subjects will receive a single dose of RO5424802 on Days 1 and 17 and rifampin daily from Days 8 to Day 20.

Outcome Measures

OutcomeResultp-value
PRIMARY
Area Under the Plasma Concentration-Time Curve From Time Zero to Extrapolated Infinite Time (AUC[0-inf]) of Alectinib
3990; 1020
PRIMARY
Maximum Observed Plasma Concentration (Cmax) of Alectinib
212; 101
SECONDARY
AUC(0-inf) of RO5468924
2250; 3970
SECONDARY
Cmax of RO5468924
90.5; 194
SECONDARY
Molecular Weight Adjusted Metabolite to Parent (M/P) Ratio for AUC(0-inf)
0.59; 3.96
SECONDARY
Molecular Weight Adjusted Metabolite to Parent (M/P) Ratio for Cmax
0.42; 1.92
SECONDARY
Area Under the Plasma Concentration-Time Curve From Time Zero to Last Measurable Concentration (AUC[0-last]) of Alectinib and RO5468924
3860; 976; 2140; 3850
SECONDARY
Time to Reach Maximum Observed Plasma Concentration (Tmax) of Alectinib and RO5468924
6.00; 4.00; 8.00; 6.00
SECONDARY
Plasma Terminal Half-Life (t1/2) of Alectinib and RO5468924
19.2; 11.0; 24.0; 23.0
SECONDARY
Apparent Oral Clearance (CL/F) of Alectinib
179; 627
SECONDARY
Apparent Volume of Distribution (Vz/F) of Alectinib
4710; 9960
SECONDARY
Total Molar Concentration of Alectinib and RO5468924 as Derived by AUC(0-inf)
13200; 10800
SECONDARY
Total Molar Concentration of Alectinib and RO5468924 as Derived by Cmax
614; 594

Eligibility Criteria

Inclusion Criteria

  • Healthy male and female volunteers, 18 to 55 years of age inclusive. Healthy status will be defined by absence of evidence of any active or chronic disease following a detailed medical and surgical history, and a complete physical examination
  • Body mass index (BMI) between 18 to 32 kg/m2 inclusive
  • Nonsmoking subjects and former smoking subjects (who have not smoked for the past six months before first dosing)
  • Female subjects must be surgically sterile or postmenopausal for the past year
  • Male subjects and their partners of childbearing potential must be willing to use two effective methods of contraception, one of which must be a barrier method (e.g., condom) during the study and for 90 days after the last drug administration

Exclusion Criteria

  • Women of childbearing potential, pregnant or lactating women, or males with female partners who are pregnant or lactating
  • Positive urine test for drugs of abuse, alcohol, or cotinine test at screening or prior to admission to the study unit
  • Suspicion of regular consumption of drug(s) of abuse including marijuana
  • Current smokers or subjects who have discontinued smoking less than six months prior to first dosing
  • History (within three months of Screening) of alcohol consumption exceeding 2 standard drinks per day on average (1 standard drink = 10 grams of alcohol). Alcohol consumption will be prohibited 72 hours prior to entry in the clinical site center and throughout the entire study (including the washout period) until discharge
  • Positive for hepatitis B, hepatitis C, or HIV infection
  • Participation in an investigational drug or device study within 45 days or 5 half-lives (whichever time period is longer) or 6 months for biologic therapies prior to first dosing
  • Any clinically significant concomitant disease or condition that could interfere with, or for which the treatment of might interfere with, the conduct of the study, absorption, distribution, metabolism or excretion of study medication, or that would, in the opinion of the PI, pose an unacceptable risk to the subject in this study
  • History of hypersensitivity to any of the additives in the RO5424802 formulation (lactose monohydrate, microcrystalline cellulose, sodium starch glycolate, hydroxypropyl cellulose, sodium lauryl sulphate, magnesium stearate)
  • Any history of hypersensitivity to or contraindication to the use of rifampin or other rifamycins or history of severe drug-related allergic reactions or hepatoxicity
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01940510). 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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