Clinical Trials

MainTitle

A Pilot Study to Assess the Feasibility of Switching, Individuals Receiving Atripla With Continuing Central Nervous System (CNS) Toxicity, to a Fixed Dose Combination of Tenofovir/Emtricitabine/Rilpivirine

This study has been completed
Sponsor
St Stephens Aids Trust


Information provided by (Responsible Party)
St Stephens Aids Trust
ClinicalTrials.gov Identifier
NCT01701882

First received: September 19, 2012
Last updated: July 24, 2017
Last Verified: July 2017
History of Changes
Purpose

Purpose

The purpose of the study is to investigate the benefits of switching away from efavirenz (which patients are taking in combination with Kivexa® or as part of the combination pill, Atripla®) in patients with central nervous system side effects (such as insomnia {difficulty with sleeping}, bad dreams etc). The investigators in this study will investigate the effect of switching to a single tablet regimen (Eviplera®) containing tenofovir, emtricitabine and rilpivirine. If patients are currently taking Atripla, rilpivirine will be the only new component of the combination.

Rilpivirine is a drug for HIV treatment, licensed for first-line treatment. In combination with Truvada®, it showed fewer side effects when compared to efavirenz in 2 other clinical studies, where patients were starting HIV treatment for the first time.

This study will also investigate the safety (in terms of other side effects and the routine blood tests which we ordinarily use to monitor your treatment) and monitor effectiveness, your viral load and CD4 counts, when you switch treatment to tenofovir/emtricitabine/rilpivirine.

Condition Intervention Phase
HIV

Drug : tenofovir/emtricitabine/rilpivirine
Phase 3

Study Type: Interventional
Study Design: Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Pilot Study to Assess the Feasibility of Switching, Individuals Receiving Atripla With Continuing Central Nervous System (CNS) Toxicity, to a Fixed Dose Combination of Tenofovir/Emtricitabine/Rilpivirine

Further study details as provided by St Stephens Aids Trust:

Primary Outcome Measures

  • Resolution of toxicity after 12 weeks [ Time Frame: 12 weeks ]
    To investigate whether switching individuals with intolerance to efavirenz-containing cART (as Atripla or Kivexa plus Efavarinz) to tenofovir/emtricitabine/rilpivirine is associated with resolution of toxicity after 12 weeks. CNS toxicity will be measured by a questionnaire based on efavirenz SPC and graded based on the ACTG adverse event scale.
Secondary Outcome Measures:
  • Resolution of toxicity after 24 weeks [ Time Frame: 24 weeks ]
    To investigate whether switching to tenofovir/emtricitabine/rilpivirine is associated with resolution of toxicity after 24 weeks. CNS toxicity will be measured by a questionnaire based on efavirenz SPC and graded based on the ACTG adverse event scale.

Enrollment: 40
Study Start Date: September 2012
Study Completion Date: November 2013
Primary Completion Date: November 2013 (Final data collection date for primary outcome measure)

Arms Assigned Interventions
Experimental: tenofovir/emtricitabine/rilpivirine
A one pill fixed dose combination of tenofovir 245mg, emtricitabine 200mg and rilpivirine 25mg once daily.
Drug: tenofovir/emtricitabine/rilpivirine
Eligibility

Eligibility

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

Criteria

Inclusion Criteria:

  • Patient volunteers who meet all of the following criteria are eligible for this trial:
    1. Is male or female aged 18 years or above
    2. Has HIV-1 infection documented in their medical notes
    3. Has signed the Informed Consent Form voluntarily
    4. Is willing to comply with the protocol requirements
    5. Has been on Atripla for at least 12 weeks OR Kivexa plus efavirenz
    6. Has an HIV-plasma viral load at screening <50 copies/mL (single re-test allowed)
    7. Has a CD4 cell count at screening >50 cells/mm3
    8. Estimated glomerular filtration rate (MDRD) >50 ml/min.
    9. Has symptomatic CNS related toxicity associated with EFV
    10. If female and of childbearing potential, is using effective birth control methods (as agreed by the investigator) and is willing to continue practising these birth control methods during the trial and for at least 30 days after the end of the trial. Note: Women who are postmenopausal for least 2 years, women with total hysterectomy, and women who have a tubal ligation are considered of non-childbearing potential
    11. If a heterosexually active male, he is using effective birth control methods and is willing to continue practising these birth control methods during the trial and until follow-up visit

  • Exclusion Criteria:
  • Patients meeting 1 or more of the following criteria cannot be selected:
    1. Infected with HIV-2
    2. Using any concomitant therapy disallowed as per SPC for the study drugs (note acid-reducing agents and interaction with rilpivirine)
    3. Has acute viral hepatitis including, but not limited to, A, B, or C
    4. Has chronic hepatitis B and/or C with AST and/or ALT >5 x ULN Note: Subjects can enter trial with chronic HBV if HBV-DNA undetectable at screen (and no detectable result in last 6 months) and with chronic HCV if not expected to require treatment during the trial period.
    5. Any investigational drug within 30 days prior to the trial drug administration
    6. Has received rilpivirine in the past
    7. Any clinical evidence of baseline resistance mutations
    8. Known allergy to lactose monohydrate, sunset yellow aluminium lake (E110), and patients with galactose intolerance, the Lapp lactase deficiency, or glucose-galactose malabsorption
    9. Severe hepatic impairment
    10. Moderate or severe renal impairment (creatinine clearance < 50ml/min)
    11. If female, she is pregnant or breastfeeding
    12. Screening blood result with any grade 3/4 toxicity according to Division of AIDS (DAIDS) grading scale, except: asymptomatic grade 3 glucose, amylase or lipid elevation or asymptomatic grade 4 triglyceride elevation (re-test allowed).
    13. Any condition (including drug/alcohol abuse) or laboratory results which, in the
    investigator's opinion, interfere with assessments or completion of the trial.

    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: NCT01701882

    Locations

    United Kingdom
    St Stephen's AIDS Trust
    London, United Kingdom, SW10 9TH

    Sponsors and Collaborators

    St Stephens Aids Trust
    More Information

    More Information


    Responsible Party: St Stephens Aids Trust  
    ClinicalTrials.gov Identifier: NCT01701882   History of Changes  
    Other Study ID Numbers: SSAT 047  
    Study First Received: September 19, 2012  
    Last Updated: July 24, 2017  

    Additional relevant MeSH terms:
    Tenofovir
    Emtricitabine
    Rilpivirine

    ClinicalTrials.gov processed this data on May 24, 2020
    This information is provided by ClinicalTrials.gov.