skip to content

Clinical Trials

MainTitle

Clinical Trial to Assess the Security of the Dose Reduction of Ritonavir in HIV-Infected Patients in Treatment With Tipranavir/Ritonavir 500/200 mg Every 12 Hours

This study has been completed
Sponsor
Germans Trias i Pujol Hospital

Collaborator
Fundacio Lluita Contra la SIDA

Information provided by (Responsible Party)
Germans Trias i Pujol Hospital
ClinicalTrials.gov Identifier
NCT00607958

First received: January 23, 2008
Last updated: July 14, 2009
Last Verified: July 2009
History of Changes
Purpose

Purpose

Tipranavir is a drug with a high antiretroviral activity, also in presence of major mutations in the protease gene. However, its necessity of being co-administered with 400 mg of ritonavir daily, limits its efficacy for the treatment of HIV-infected patients, due to the high incidence of gastrointestinal adverse events. Nevertheless, tipranavir plasma though concentrations were higher than the proposed minimum effective concentration for patients with previous experience with protease inhibitors (PI) in half of patients treated with tipranavir/ritonavir at 500/100 mg dose every 12 hours. Furthermore, when the number of mutations in the protease gene is limited, there are no differences in the reduction of the viral load between patients treated with tipranavir/ritonavir at 500/200 mg and 500/100 mg every 12 hours. At last, the efficacy of tipranavir treatment has been more closely related with the inhibition quotient (IQ) than with concentrations considered isolated.

Considering the previous arguments, it can be hypothesized that, basing in every subject IQ, it could be possible to identify those patients HIV-infected in treatment with tipranavir/ritonavir at 500/200 mg every 12 hours that could take advance of the reduction of ritonavir to 100 mg every 12 hours, without compromising the viral replication control. This strategy could improve the tolerability to the treatment, what could result in a better adherence and less proportion of treatment abandon due to this reason

Condition Intervention Phase
HIV Infections

Drug : tipranavir/ritonavir (dose reduction)
Phase 4

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Clinical Trial to Assess the Security of the Dose Reduction of Ritonavir in HIV-Infected Patients in Treatment With Tipranavir/Ritonavir 500/200 mg Every 12 Hours

Further study details as provided by Germans Trias i Pujol Hospital:

Primary Outcome Measures

  • Proportion of patients with viral load <50 copies/mL [ Time Frame: Basal, week 2, week 4, week 8, week 12 week 24, week 36 and week 48. ]
Secondary Outcome Measures:
  • Proportion of patients that show a tipranavir IQ >60 while treated with tipranavir/ritonavir 500/200 mg every 12 hours [ Time Frame: Screening ]
  • Proportion of patients that maintain a tipranavir IQ >=40 while treated with tipranavir/ritonavir 500/100 mg every 12 hours [ Time Frame: Basal, week 2, week 4, week 8, week 12 week 24, week 36 and week 48. ]
  • Change in CD4 lymphocytes count after 24 and 48 weeks' follow-up [ Time Frame: Week 24 and week 48 ]
  • Incidence and severity of adverse events after 24 and 48 weeks' follow-up [ Time Frame: Week 24 and week 48 ]
  • Change in lipid profile (total cholesterol, HDL-cholesterol. LDL-cholesterol and triglycerides) after 24 and 48 weeks' follow-up [ Time Frame: Week 24 and week 48 ]
  • Change in hepatic enzymes (AST, ALT and GGT) after 24 and 48 weeks' follow-up [ Time Frame: Week 24 and week 48 ]
  • In patients with virological failure, incidence of new mutations in the protease gene [ Time Frame: When virological failure ]

Enrollment: 15
Study Start Date: December 2007
Study Completion Date: May 2009
Primary Completion Date: May 2009 (Final data collection date for primary outcome measure)

Arms Assigned Interventions
Experimental: 1
dose reduction
Drug: tipranavir/ritonavir (dose reduction)

tipranavir/ritonavir 500/100 BID

Detailed Description:

Tipranavir efficacy as a rescue treatment in HIV-infected patients was assessed in the RESIST studies, which included patients with a wide antiretroviral experience who were found in viral failure despite being on PI-based antiretroviral therapy and in which resistance test showed the presence of major mutations in the protease gene. In those studies treatment with tipranavir/ritonavir at 500/200 mg dose every 12 hours was related with a major probability of achieving undetectable viral load after a 48 weeks follow-up, compared with conventional PI (33.6% vs. 15.3%, respectively). However, tipranavir clinical efficacy can be limited by the appearance of adverse events, mainly on a gastrointestinal level, but also altering the lipid profile or elevating the transaminase plasmatic concentration.
According to the data of the BI 1182.52 study, response to tipranavir is related to its plasma trough concentration. So, concentrations higher than 20 mmol/L (10 times the IC90 adjusted by the binding to proteins of HIV PI-resistant-strains) are related with a major probability of achieving the viral replication suppression. This concentration was achieved by the 77% and the 48% of patients who received tipranavir 500 mg every 12 hours co-administered with 200 and 100 mg of ritonavir every 12 hours respectively. Furthermore, viral load diminution was similar between patients treated with 100 or with 200 mg of ritonavir every 12 hours, as long as the number of mutations was less than 20. These data states the importance of putting together virological (mutations in the protease gene) and pharmacokinetic data (trough levels) so the antiretroviral treatment benefit can be maximized. The subanalysis that included 157 patients of the BI 1182.52 study and 311 patients of the RESIST study showed that virological response in patients with treatment with tipranavir/ritonavir was better in patients with an IQ higher than 25-50.
With this data the following conclusions can be inferred: tipranavir is a drug with a high antiretroviral activity, also in presence of major mutations in the protease gene. However, its necessity of being co-administered with 400 mg of ritonavir daily, limits the efficacy for the treatment of HIV-infected patients, due to a high incidence of gastrointestinal adverse events. Nevertheless, trough levels of tipranavir was over the proposed minimum effective concentration for patients with previous experience with protease inhibitors (IP). Furthermore, as the number of mutations in the protease gene is limited, there are no differences in the reduction of the viral load between patients treated with tipranavir/ritonavir at 500/200 mg and 500/100 mg every 12 hours. At last, the efficacy of tipranavir treatment has been closely related with the inhibition quotient (IQ) than with concentrations obtained considered isolated.
Considering the previous arguments, it can be hypothesized that, basing in every subject IQ, it could be possible to identify those patients HIV-infected in treatment with tipranavir/ritonavir at 500/200 mg every 12 hours that could take advance of the reduction of ritonavir to 100 mg every 12 hours, without compromising the viral replication control. This strategy could improve the tolerability to the treatment, what could result in a better adherence and less proportion of treatment abandon due to this reason.

Eligibility

Eligibility

Ages Eligible for Study: 18 Years and older  
Sexes Eligible for Study: All  
Accepts Healthy Volunteers: No  

Criteria

Inclusion Criteria:

    1. Age +=18 years.
    2. HIV-infected patients.
    3. Stable antiretroviral treatment including tipranavir/ritonavir 500/200 every 12 hours for at least 4 weeks.
    4. HIV viral load <50 copies/mL for at least 12 weeks.
    5. Resistance test (Genotype or Virtual Phenotype) before starting tipranavir treatment.
    6. Tipranavir IQ +=60.
    7. Subject able to follow the treatment period.
    8. In women, negative pregnancy test or not in fertile age (defined as at least one year from menopause or undergoing any surgical sterilisation technique), or undertaking to use a barrier contraceptive method during the study.
    9. Signature of the informed consent.


Exclusion Criteria:
    1. AIDS-defining illness in the last 4 weeks.
    2. Suspicion of unsuitable antiretroviral treatment compliance.
    3. In women, pregnancy or breastfeeding.
    4. Record or suspicion of incapability to cooperate as appropriate.

contacts and locations

Contacts and Locations

Choosing to participate in a study is an important personal decision.Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below.For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00607958

Locations

Spain
Germans Trias i Pujol Hospital
Badalona, Barcelona, Spain, 08916

Sponsors and Collaborators

Germans Trias i Pujol Hospital
Fundacio Lluita Contra la SIDA

Investigators

Principal Investigator: Molto Jose, MD,PhD Germans Trias i Pujol Hospital
More Information

More Information


Responsible Party: Lluita Sida Foundation, Lluita Sida Foundation  
ClinicalTrials.gov Identifier: NCT00607958   History of Changes  
Other Study ID Numbers: TPVRTV_500100_IQ  
Study First Received: January 23, 2008  
Last Updated: July 14, 2009  

Keywords provided by Germans Trias i Pujol Hospital:

Tipranavir
ritonavir
dose reduction
inhibitory quotient

Additional relevant MeSH terms:
HIV Infections
Ritonavir
Tipranavir

ClinicalTrials.gov processed this data on October 16, 2017
This information is provided by ClinicalTrials.gov.