Switching From Protease Inhibitor (PI) to Etravirine in HIV-1 Infected Subjects With Viremia Suppression

Phase 3

Completed

• Conditions: HIV
• Interventions: Drug: Continue with the same antiretroviral regimen; Drug: Etravirine 400 mg dissolved in water every 24 hours

• Registration Number: NCT01034917
• Lead Sponsor: Germans Trias i Pujol Hospital

Brief Summary

This is a 48 week randomized, prospective, controlled, open-label, proof-of-concept pilot clinical trial.

Patients with HIV-1 infection on HAART PI-based regimen will be randomized to switch from the PI to etravirine (400 mg dissolved in water every 24 hours) or to continue with the same approach.

The aim of the study is to compare the virological efficacy of the etravirine-based regimen with standard PI-containing regimen.

Detailed Description

Etravirine is a second generation non-nucleoside analogue reverse transcriptase inhibitor (NNRTI) approved by the U.S. Food and Drug Administration (FDA) in January 2008 and by the European Medicines Agency in September 2008 for clinical use in adults with incomplete virologic suppression and resistance to previous NNRTI and other antiretroviral classes.

A question that has not been explored is whether subjects with sustained undetectable HIV-1 RNA-levels experiencing antiretroviral-related toxicity can safely switch their current PI to etravirine. This treatment strategy could allow improvements in tolerability and lipid profile and would permit an easy posology (400 mg dissolved in water every 24 hours). We designed a proof-of-concept study to test the efficacy and safety of switching from a Protease Inhibitor (PI) to etravirine in subjects with viral suppression as an antiretroviral strategy of simplification therapy, based on the high antiviral potency, low toxicity, together with its easy posology (in water dissolution).

Patients with HIV-1 infection on HAART PI-based regimen will be randomized to switch from the PI to etravirine (400 mg dissolved in water every 24 hours) or to continue with the same approach.

The primary endpoint would be the percentage of patients who maintain virological suppression at week 48.

Study Timeline

• Study Start: 2009-12
• Study First Submitted: 2009-12-17
• Study First Submitted QC: 2009-12-17
• Study First Posted: 2009-12-18
• Primary Completion: 2011-12
• Study Completion: 2011-12
• Status Verified: 2020-01
• Last Update Submitted: 2020-01-30
• Last Update Posted: 2020-01-31

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 43

Inclusion Criteria

1. Adult patient having a diagnosis of HIV-1 infection.

2. Antiretroviral therapy started at least 12 months before, always with a HAART combination including 2 NRTIs plus a PI.

3. Maintained undetectable plasma HIV-1 RNA (VL < 50 copies/mL) since the beginning of antiretroviral therapy, for at least 6 months.

4. Absence of suspected or documented resistance mutations in the RT associated to NNRTIs or to any NRTI.

5. Patient having at least one of the following conditions:

   • Dyslipemia (LDL cholesterol >130 mg/dL or triglycerides > 350 mg/dL) derived from their current PI regimen or current use of lipid-lowering agents due to dyslipemia,
   • Antiretroviral-related gastrointestinal disturbances, or
   • Low patient's satisfaction associated with the current regimen posology (BID regimen, ritonavir use, ritonavir intolerance...).

6. Good treatment adherence.

7. Voluntary written informed consent.

Exclusion Criteria

1. Previous therapy with mono or dual antiretroviral therapies after initial of HAART era.
2. Previous antiretroviral treatment failures, treatment interruptions (A) or blips (B) in viral load (VL > 50 copies/mL).
3. Acute infections or uncontrolled chronic infection in the 2 months previous to the inclusion.
4. Pregnancy or fertile women willing to be pregnant.
5. Clinically significant malabsorption syndrome within 30 days prior to randomization.

(A) Patients who in the past made any interruption of treatment (provide that it has not been in the last year) may be considered candidates for the study, if they meet other criteria for inclusion, since the break in the treatment should not assume the emergence of mutations.

(B) Small blips that are preceded or forwarded by 2 undetectable viral loads will not be taken in care.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Control group	Continue with the same antiretroviral regimen	Continue with the same antiretroviral regimen
Etravirine group	Etravirine 400 mg dissolved in water every 24 hours	To switch from the PI to Etravirine 400 mg dissolved in water every 24 hours

Primary Outcome Measures

Name	Time	Method
Viral load	week 48 after baseline

Secondary Outcome Measures

Name	Time	Method
CD4+/CD8+ T lymphocytes count	evolution from baseline to week 48
Genotypic test	if virologic failure occurs
Cardiovascular risk assessed by the SCORE equation	evolution from baseline to week 48
Patient's satisfaction assessed by 2 scales of type Likert	evolution from baseline to week 48
Lipid profile: total, HDL-, LDL-cholesterol and triglyceride levels	evolution from baseline to week 48
Etravirine plasma trough concentration	Week 4
Administration of lipid-lowering drugs throughout the study	from baseline to week 48
Adverse events related to antiretroviral treatment	from baseline to week 48

Trial Locations

Locations (1)

Germans Trias i Pujol University Hospital; 🇪🇸 Badalona, Barcelona, Spain