Drug Drug Interaction of BI 201335 and Tenofovir
This study has been completed.
Information provided by (Responsible Party):
First received: April 20, 2011
Last updated: November 16, 2011
Last verified: November 2011
The objective of this study is to evaluate the drug-drug interaction potential between BI 201335 and concomitantly administered tenofovir which is used in treatment regimens for HIV infection and/or Hepatitis B infection. Results of this study will serve as a basis for guidance of dose adjustments or other precautionary measures when BI201335 and tenofovir are coadministered.
Drug: tenofovir/BI 201335
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
||Effect of Multiple Dosing With 240 mg BID BI 201335 on the Steady State Pharmacokinetics of 300mg QD Tenofovir and Effect of Multiple Dosing With 300mg QD Tenofovir on Steady State BI 201335 Pharmacokinetics in Healthy Male and Female Volunteers
Primary Outcome Measures:
- Comparison of steady-state pharmacokinetics of AUC0-24 of tenofovir on Day 7 with Day 15 [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]
- Comparison steady-state pharmacokinetics of AUC0-12 of BI 201335 on Day 15 and on Day 22. [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]
- Comparison of steady-state pharmacokinetics of Cmax of tenofovir on Day 7 with Day 15 [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]
- Comparison of steady-state pharmacokinetics of C24hr of tenofovir on Day 7 with Day 15 [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]
- Comparison of steady-state pharmacokinetics of Cmax of BI 201335 on Day 15 and Day22 [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]
- Comparison of steady-state pharmacokinetics of C12hr of BI 201335 on Day 15 and Day 22 [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Number of adverse events during the trial [ Time Frame: approximately 4 weeks ] [ Designated as safety issue: No ]
- Intensity of adverse events during the trial [ Time Frame: approximately 4 weeks ] [ Designated as safety issue: No ]
| Study Start Date:
| Primary Completion Date:
||June 2011 (Final data collection date for primary outcome measure)
Experimental: sequence 1
tenofovir medium dose once daily (qd) for first 15 days; BI 201335 medium dose twice daily (bid) on days 8 through day 22 (morning dose on day 22 only)
Drug: tenofovir/BI 201335
tenofovir medium dose once daily (qd) for first 15 days; BI 201335 medium dose twice daily (bid) on days 8 through 22 with last dose on morning of day 22
|Ages Eligible for Study:
||18 Years to 55 Years
|Genders Eligible for Study:
|Accepts Healthy Volunteers:
- Healthy males and female subjects and according to medical history, including the physical examination, vital signs (blood pressure, pulse rate), 12-lead electrocardiogram and clinical laboratory tests; all with acceptable findings.
- Age =18 to =55 years
- Weighing at least 50 kg, and body mass index >=18.5 and BMI <=29.9 kg/m2 (Body Mass Index).
- Volunteers must not leave the research unit, during the entire length of the study and must be willing to comply with the protocol and complete all study-related activities.
- Any finding of the medical examination (including blood pressure, pulse rate and electrocardiogram) deviating from normal and of clinical relevance, as assessed by the investigator.
- Active diseases of the gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, musculoskeletal, immunologic, rheumatologic, hormonal, neurological system, clinically relevant electrolyte disorders or bleeding disorders that require current medical treatment.
- Diseases of the central nervous system or psychiatric disorders.
- History of photosensitivity or recurrent rash.
- History of orthostatic hypotension, fainting spells or blackouts.
- Chronic or clinically relevant acute infections.
- History of allergy/hypersensitivity (including drug allergy) which is deemed relevant.
- Intake of drugs with a long half-life >24:00 hours within at least one month or less than ten half lives of the respective drug before enrollment in the study (with the exception of hormonal contraceptives).
- Use of any drugs which might influence the results of the trial up to 7 days prior to enrolment as nutraceuticals and herbal remedies that would interfere with either the absorption, distribution or metabolism of BI 201335 NA, or that prolong the QT/QTc interval.
- Use of any investigational drug within 30 days prior to enrollment; or the planned use of any investigational drug during the course of the current study.
- Smoking (>10 cigarettes or >3 cigars or >3 pipes/day)
- Inability to abstain from smoking more than 3 cigarettes/day during the period of dosing with study medication.
- Drug and alcohol abuse (>60g/day).
- Blood donation (more than 100 mL within four weeks prior to administration or during the trial).
- Excessive physical activities within one week prior to administration or during the trial.
- Any laboratory value outside the reference range that is of clinical relevance at screening, according to the judgment of the investigator, and in consultation with the clinical monitor.
- Known elevated liver enzymes in past with any compound (experimental or marketed).
- Concomitant administration of any food product known to alter P450 enzyme activity such as grapefruit juice, Seville oranges, St. John's Wort.
- Concomitant administration of oral contraceptives (subjects who stopped oral contraceptives at least 7 days prior to Day 1 may be included.
- Inadequate venous access.
- A marked baseline prolongation of QT/QTc interval (e.g., repeated demonstration of a QTcF, or QTcB interval >450 ms).
- Infection with hepatitis B (HBV), or hepatitis C virus (HCV),
- Positive test for HIV-1 or HIV-2. For women of child bearing potential (WOCBP)
- Pregnancy or planning to become pregnant within 2 months of study completion
- Positive pregnancy test at screening visit
- No proof of sterilization, or not willing or unable to consistently use an acceptable method of double barrier contraception including IUD, or diaphragm with spermicidal cream/jelly and condoms for male partner, during and up to 3 months after completion/termination of the trial.
Lactation period with active breastfeeding from time of screening to 30 days after end of trial visit.
For male subjects
- No proof of sterilization, or not willing or unable to consistently use an acceptable method of double barrier contraception including a condom each time and female partner of child bearing potential consistently uses oral birth control pills, or an IUD, or a diaphragm with spermicidal cream/jelly). Male subjects must not father a child from administration of the first dose and up to 3 months after the last dose of study medication.
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Please refer to this study by its ClinicalTrials.gov identifier: NCT01340196
|1220.50.0001 Boehringer Ingelheim Investigational Site
|Buffalo, New York, United States |
No publications provided
History of Changes
|Other Study ID Numbers:
|Study First Received:
||April 20, 2011
||November 16, 2011
||United States: Food and Drug Administration
Additional relevant MeSH terms:
ClinicalTrials.gov processed this record on April 16, 2015
Molecular Mechanisms of Pharmacological Action
Nucleic Acid Synthesis Inhibitors
Reverse Transcriptase Inhibitors