Effects of Tipranavir (TPV) and Ritonavir (RTV) on the Pharmacokinetic Characteristics of Tenofovir Disoproxil Fumarate in Healthy Volunteers

Phase 1

Completed

• Conditions: Healthy
• Interventions: Drug: Tipranavir high dose; Drug: Tipranavir low dose; Drug: Ritonavir high dose; Drug: Ritonavir low dose; Drug: Tenofovir disoproxil fumarate

• Registration Number: NCT02251145
• Lead Sponsor: Boehringer Ingelheim

Brief Summary

Study to characterise the effects of two dose combinations of tipranavir/ritonavir (TPV 500 mg/RTV 100 mg and TPV 750 mg/RTV 200 mg) administered BID, on the pharmacokinetics of tenofovir disoproxil fumarate as well as the effects of tenofovir disoproxil fumarate on the pharmacokinetics of tipranavir/ritonavir.

Detailed Description

Not available

Study Timeline

• Study Start: 2002-05
• Primary Completion: 2002-06
• Status Verified: 2014-09
• Study First Submitted: 2014-09-25
• Study First Submitted QC: 2014-09-25
• Last Update Submitted: 2014-09-25
• Study First Posted: 2014-09-29
• Last Update Posted: 2014-09-29

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 49

Inclusion Criteria

1. Ability and willingness to give written informed consent in accordance with institutional and regulatory guidelines and to comply with the investigational nature of the study and the related requirements
2. Healthy males or females between 18 and 60 years of age inclusive
3. A Body Mass Index >18.5 and <30 kg/m2
4. Ability to swallow numerous large capsules without difficulty
5. Reasonable probability for completion of the study, in the opinion of the investigator
6. Acceptable laboratory values that indicate adequate baseline organ function are required at the time of screening. Laboratory values are considered to be acceptable if severity <= Grade1 based on the AIDS Clinical Trials Group (ACTG) Division of AIDS (DAIDS) Grading Scale. All abnormal laboratory values > Grade 1 (e.g., creatine phosphokinase (CPK), amylase, triglycerides) are subject to approval by the BIPI clinical monitor. Cholesterol <= 240mg/dL at the time of screening is necessary for study entry
7. Acceptable medical history, physical examination and ECG are required prior to entering the study
8. Willingness to abstain from alcohol for 48 hours prior to Study Day 0 and abstain from alcohol for the duration of the study. In addition, Cabernet Sauvignon must not have been ingested within 15 days prior to Day 0 (Visit 2)
9. Willingness to abstain from ingesting grapefruit and grapefruit juice within 15 days of Day 0, Visit 2 and for the duration of the study
10. Willingness to abstain from ingesting Seville oranges, strawberries or strawberry extract, garlic supplements, St. John's Wort, Milk Thistle, or methylxanthine-containing drinks or food (coffee, tea, cola, energy drinks, chocolate, etc) within 72 hours of pharmacokinetic (PK) sampling days
11. Willingness to abstain from use of tobacco products for the duration of the study
12. Urine drug screen negative for illegal non-prescription drugs
13. Negative HIV serology
14. Negative for Hepatitis B surface antigen and Hepatitis C

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Exclusion Criteria

1. Female subjects who are of reproductive potential who:

   • Have a positive serum B-HCG at Visit 1 or 2 or
   • Have not been using regular oral contraception (combined oestrogen and progestogen pill or progestogen only pill) for 3 months and a barrier contraceptive method for at least 30 days prior to Visit 3 (Day 1) or a barrier contraceptive method for at least 3 months prior to Visit 3 (Day 1) or
   • Are not willing to use a reliable method of double-barrier contraception (such as diaphragm with spermicidal cream/jelly or condoms with spermicidal foam)during the trial and 30 days after completion/termination or
   • Are breast-feeding

2. Participation in another trial with an investigational medicine for 30 days prior to Day 0 (Visit 2)

3. Ingestion of any known enzyme altering drug (such as phenothiazines, cimetidine, barbiturates, ketoconazole, fluconazole, rifampin, steroids, and herbal medications) for 30 days prior to Day 0 (Visit 2). Use of any other herbal/complementary treatment must be discussed in advance with the monitor and permission obtained prior to study entry

4. Ingestion of grapefruit, grapefruit juice, and Cabernet Sauvignon within 15 days prior to Day 0 (Visit 2)

5. Ingestion of Seville oranges, strawberries or strawberry extract, garlic supplements, St. John's Wort, Milk Thistle, or methylxanthine-containing drinks or food (coffee, tea, cola, energy drinks, chocolate, etc) within 72 hours of PK sampling days

6. Ingestion of antibiotics within 10 days prior to Day 0 (Visit 2)

7. Inability to comply with investigator's instructions

8. History of gastrointestinal, hepatic, or renal disorders within 60 days

9. History of alcohol abuse

10. Current use of cigarettes defined as greater than 10 cigarettes per day or rolling/pipe tobacco equivalent

11. Blood or plasma donations within 30 days prior to Day 0 (Visit 2)

12. Subjects with a seated systolic blood pressure either <100 mm Hg or >150 mm Hg; resting heart rate either <50 beats/min or >100 beats/min

13. Subjects with a history of any illness or allergy that, in the opinion of the investigator, might confound the results of the study or pose additional risk in administering tipranavir or ritonavir or tenofovir disoproxil fumarate to the subject

14. Subjects who have had an acute illness within 2 weeks prior to Day 0 (Visit 2)

15. Subjects who are currently taking any over-the-counter drug within 7 days prior to Day 0, (Visit 2) or who are currently taking any prescription drug that, in the opinion of the investigator in consultation with the clinical monitor and pharmacokineticist, might interfere with either the absorption, distribution or metabolism of the test substances

16. Hypersensitivity to tipranavir, ritonavir, or tenofovir disoproxil fumarate

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
tipranavir/ritonavir high dose	Ritonavir high dose	-
tipranavir/ritonavir high dose	Tipranavir high dose	-
tipranavir/ritonavir low dose	Tipranavir low dose	-
tipranavir/ritonavir low dose	Ritonavir low dose	-
tipranavir/ritonavir low dose	Tenofovir disoproxil fumarate	-
tipranavir/ritonavir high dose	Tenofovir disoproxil fumarate	-

Primary Outcome Measures

Name	Time	Method
Area under plasma concentration time curve from 0-24 hours (AUC0-24) for tenofovir	up to 24 hours
Area under plasma concentration time curve from 0-12hours (AUC0-12) for tipranavir/ritonavir	up to 12 hours
Drug concentration in plasma at 12 hours after administration (C12h) for tipranavir/ritonavir	up to 12 hours
Maximum plasma concentration (Cmax)	up to 24 hours
Drug concentration in plasma at 12 hours after administration (C12h) for tenofovir	up to 12 hours

Secondary Outcome Measures

Name	Time	Method
Trough plasma concentration at steady state (Cmin)	up to 24 hours
Oral clearance (CL/F)	up to 24 hours
Number of subjects with clinically significant findings in physical examination	up to 14 days
Number of subjects with clinically significant findings in laboratory tests	up to 14 days
Apparent terminal half life (T1/2)	up to 24 hours
Time of maximum concentration (Tmax)	up to 24 hours
Number of subjects with clinically significant findings in vital signs (pulse rate, blood pressure)	up to 14 days
Mean residency time (MRT)	up to 24 hours
Apparent volume of distribution during the terminal elimination phase, divided by F (bioavailability factor) (Vz/F)	up to 24 hours
Number of subjects with clinically significant findings in electrocardiogram	up to 14 days
Number of subjects with adverse events	up to 14 days
Maximum plasma concentration at steady state (Cmax,ss)	up to 24 hours