Effects of Tipranavir/Ritonavir on the Pharmacokinetic Characteristics of Triple Drug Nucleoside and Non-nucleoside Reverse Transcriptase Inhibitor Therapy in HIV-1-infected Subjects

HIV Infections Clinical Trial

Official title:

An Open Label Multinational Study of the Effects of Three Dose Pairs of Tipranavir/Ritonavir (b.i.d.) on the Pharmacokinetic Characteristics of Protocol -Defined, Baseline, Triple Drug Nucleoside and Non-nucleoside Reverse Transcriptase Inhibitor Therapy in HIV-1-infected Subjects.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02251223
• Other study ID #: 1182.6
• Status: Completed
• Phase: Phase 1/Phase 2
• First received: September 25, 2014
• Last updated: September 25, 2014
• Start date: February 2001

Study information

• Verified date: September 2014
• Source: Boehringer Ingelheim
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug AdministrationGermany: Federal Institute for Drugs and Medical DevicesFrance: Agence Nationale de Sécurité du Médicament et des produits de santéDenmark: Danish Health and Medicines AuthoritySpain: Agencia Española de Medicamentos y Productos SanitariosBelgium: Federal Agency for Medicines and Health Products, FAMHP
• Study type: Interventional

Clinical Trial Summary

Primary: Sequentially determine the effects of three dose combinations of tipranavir (TPV) / ritonavir (RTV) (administered b.i.d.), TPV 1250 mg/RTV 100 mg vs. TPV 750 mg/RTV 100 mg vs. TPV 250 mg/RTV 200 mg on the steady-state pharmacokinetics of zidovudine, lamivudine, stavudine, didanosine, abacavir, nevirapine and efavirenz at approved doses. The three treatment groups will be enrolled sequentially starting with the highest tipranavir dosage group first and ending with the lowest tipranavir dosage group.

Secondary: A) To assess the effects of zidovudine, lamivudine, stavudine, didanosine, abacavir, nevirapine, and efavirenz on the pharmacokinetics of tipranavir/ritonavir compared to historical controls.

B) To assess the safety of three tipranavir/ritonavir combinations when used in combination with protocol defined antiretrovirals.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 208
• Est. primary completion date: February 2002
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Signed informed consent prior to trial participation

2. Between 18 and 75 years of age inclusive

3. Female subjects of child bearing potential are required to use a barrier contraceptive method for at least 12 weeks prior to administration of study medication, during study medication administration, and for 28 days after the end of the study

4. Ability to swallow capsules without difficulty

5. A Body Mass Index (BMI) between 11 and 50 kg/m2

6. Reasonable probability for completion of the study

7. Acceptable screening laboratory values. All laboratory values = Grade I (e.g., creatine phosphokinase (CPK), amylase, triglycerides) are permissible if documentation of stability for 2 months or more is available. Abnormalities > Grade I are subject to approval by BI clinical monitor or designee

8. Acceptable medical history, physical examination, ECG, and chest X-ray prior to entering the treatment phase of the study

9. Willingness to abstain from alcohol from Day -2 to Day 23

10. Willingness to abstain from ingesting grapefruit, grapefruit juice, Seville oranges or orange marmalade from Day -2 to Day 23

11. Negative urine drug screen for drugs of abuse. Subjects on methadone or equivalent narcotic maintenance programs will be permitted to enter the study

12. Documented HIV-1 RNA load (by PCR) at screening of =20,000 copies/mL for at least twelve weeks. Acceptable documentation would include laboratory data, a letter or a verbal report from another provider noted in the subject records.

13. Stable doses of approved NRTIs and NNRTIs 2 for a minimum of twelve weeks prior to study Day 0. Subjects on efavirenz must be able to tolerate daily morning (8:00 a.m.) dosing starting at screening period and for 22 days of the study. Subjects receiving bid ddI must be willing to accept a change to the once a day delayed release (EC) formulation

Exclusion Criteria:

1. Female subjects who:

• have a positive serum pregnancy test at Screening Period Day -14 to -7

• are breast feeding

2. Receipt of any other investigational medicine for 30 days prior to Day 0

3. Receipt of any known cytochrome P450 3A4 (CYP3A4) altering drug i.e. phenothiazines, cimetidine, barbiturates, ketoconazole, fluconazole, rifampin, steroids and herbal medications for 30 days prior to Day 0. No antibiotics permitted within 10 days prior to Day 0

4. Ingestion of grapefruit, grapefruit juice, Seville oranges or orange marmalade within 2 days of study entry (Day 0)

5. Blood or plasma donations (>100 ml total) for research or altruistic reasons within 30 days prior to Day 0

6. Seated systolic blood pressure either <100 mm Hg or >150 mm Hg; resting heart rate either <50 beats/minute or >90 beats/minute

7. History of any illness, including malabsorption, irregular food intake or gastrointestinal intolerance, or allergy that, in the opinion of the investigator, might confound the results of the study or pose additional risk in administering TPV/RTV

8. Any acute illness within 2 weeks prior to Day 0

9. Subjects who are currently taking any over-the-counter drug within 7 days prior to Day 0, or who are currently taking any prescription drug that, in the opinion of the investigator (in consultation with the BI medical monitor and/or pharmacokineticist), might interfere with either the absorption, distribution or metabolism of the TPV/RTV

10. Hypersensitivity to TPV, RTV or sulfonamide containing drugs

11. Using the adherence diary, subject has less than 100% documented adherence for the last 14 doses (7 days) of baseline antiretroviral medications prior to Day 0. Subjects has less than 100% adherence for the last 7 doses (7 days) of efavirenz and ddI (delayed release) prior to Day 0

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Primary Purpose: Treatment

Related Conditions & MeSH terms

• HIV Infections

Intervention

Drug:
• Tipranavir low dose

• Tipranavir medium dose

• Tipranavir high dose

• Ritonavir low dose

• Ritonavir high dose

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Boehringer Ingelheim

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in trough plasma concentration (Cmin,ss) for non-nucleoside reverse transcriptase inhibitor (NNRTI)	stratified by substance	baseline, up to day 23	No
Primary	Change in area under plasma concentration-time curve over dosing interval (AUC0-t) for nucleoside reverse transcriptase inhibitor (NRTI)	stratified by substance	baseline, up to day 22	No
Primary	Change in area under plasma concentration-time curve from 0 to 12 hours for didanosine (ddI)		baseline, up to day 22	No
Secondary	Cmin,ss	stratified by substance	up to day 23	No
Secondary	AUC0-t	stratified by substance	up to day 23	No
Secondary	Maximum plasma concentration (Cmax)	stratified by substance	up to day 23	No
Secondary	Time of maximum plasma concentration (Tmax)	stratified by substance	up to day 23	No
Secondary	Oral clearance (Cl/F)	stratified by substance	up to day 23	No
Secondary	Apparent terminal half life (t1/2)	stratified by substance	up to day 23	No
Secondary	Change in CD4 cell count		up to day 23	No
Secondary	Change in HIV-1 RNA levels		up to day 23	No
Secondary	Number of patients with clinically significant findings in laboratory tests		up to 25 weeks	No
Secondary	Number of patients with adverse events		up to 25 weeks	No

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