PI or NNRTI as First-line Treatment of HIV in West Africa - the PIONA Trial

This study is ongoing, but not recruiting participants.
Sponsor:
Collaborators:
Aarhus University Hospital Skejby
Bandim Health Project
Ministry of Health, Guinea-Bissau
Abbott
Information provided by (Responsible Party):
University of Aarhus
ClinicalTrials.gov Identifier:
NCT01192035
First received: August 9, 2010
Last updated: December 30, 2013
Last verified: December 2013

August 9, 2010
December 30, 2013
May 2011
April 2014   (final data collection date for primary outcome measure)
Fraction of patients with viral load suppression <400 copies/ml [ Time Frame: 12 months after enrolment ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01192035 on ClinicalTrials.gov Archive Site
  • Fraction of patients with viral load suppression <50 copies/ml [ Time Frame: 12 months after enrolment ] [ Designated as safety issue: No ]
  • Increment of CD4+ cell count of at least 100 cells/µL [ Time Frame: 12 months after enrolment ] [ Designated as safety issue: No ]
  • Development of ≥1 resistance mutations involving the treatment regimens used in patients with viral load >400 copies/ml [ Time Frame: 12 months after enrolment ] [ Designated as safety issue: No ]
  • Frequency of adverse events and severe adverse events [ Time Frame: Within 12 months ] [ Designated as safety issue: Yes ]
  • Compliance. [ Time Frame: Within 12 months ] [ Designated as safety issue: No ]
    Compliance defined as the actual amount of medicine taken compared to the planned amount for the same treatment period. A pill count is carried out at each visit.
  • Incidence of tuberculosis. [ Time Frame: Within 12 months ] [ Designated as safety issue: No ]
  • Death. [ Time Frame: Within 12 months ] [ Designated as safety issue: Yes ]
    Death at 12 month follow-up. Any patient lost to follow-up will be attempted visited at home by a field assistant 1 month after latest visit due. Information on patient death from family or neighbors will be recorded as a mortality event and a verbal autopsy conducted.
  • Weight [ Time Frame: Within 12 months ] [ Designated as safety issue: No ]
    Increase in body mass index (BMI) and frequency of severe weight loss (>10% of presumed or measured body weight).
  • Plasma cytokine levels [ Time Frame: Within 12 months ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
PI or NNRTI as First-line Treatment of HIV in West Africa - the PIONA Trial
PI or NNRTI as First-line Treatment of HIV in a West African Population With Low Adherence - the PIONA Trial

BACKGROUND: Since 1996 the combination of three or more drugs has been the mainstay of human immunodeficiency virus (HIV) treatment. The most important types of drugs are called nucleotide reverse transcriptase inhibitors (NRTIs), non-nucleotide reverse transcriptase inhibitors (NNRTIs) and protease inhibitors (PIs) Response to treatment is measured as increasing CD4+ cell count and decreasing HIV viral load. A major problem is the development of resistance. NNRTIs are recommended as part of first-line treatment of HIV in Africa but many Africans have a slower NNRTI clearance than Caucasians making them more susceptible for development of resistance in case of treatment interruptions. PIs might therefore be a better option in an African setting with low adherence.

AIM: To evaluate two different treatment regimens in HIV-1 infected patients:

A) A NNRTI (efavirenz/nevirapine) based regimen and B) A PI (ritonavir-boosted lopinavir) based regimen with regard to treatment outcomes. HYPOTHESIS: Treatment with a PI will be superior to treatment with a NNRTI due to less development of resistance.

METHODS: Treatment-naïve adult HIV-1 patients enrolled in an existing cohort The West African Retrovirus and Acquired Immune Deficiency (WARAID) cohort in Guinea Bissau with CD4+ cell count ≤ 350 cells/µL and/or clinical signs of immune suppression (World Health Organization (WHO) clinical stage 3 or 4) will be randomised 1:1 to: Treatment A: 2 NRTIs (lamivudine and either zidovudine or stavudine) and 1 NNRTI (efavirenz or nevirapine) or Treatment B: 2 NRTIs (same as in treatment A) and 1 PI (ritonavir-boosted lopinavir). Primary outcome: Viral load suppression <400 copies/ml 12 months after enrolment.

PERSPECTIVES: Guidelines for treatment of HIV in Africa are more or less a copy of the guidelines used in Europe and North America. Genetic differences in pharmacokinetics, more women infected in Africa and difficulties ensuring good adherence mean that results obtained from Caucasian patients are not directly transferrable to African patients. The results of this study will hopefully help guiding the treatment of HIV in Africa in the future. The investigators believe the HIV infected people in West Africa deserve the same evidence-based medicine as in developed countries.

Not Provided
Interventional
Phase 4
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
HIV-1
  • Drug: Efavirenz or Nevirapine
    2 NRTIs (lamivudine 150 mg "bis in die - twice a day" (BID) and either zidovudine 300 mg BID if hemoglobin is ≥ 8 g/L or stavudine 30 mg BID if hemoglobin is < 8 g/L) and 1 NNRTI (efavirenz 600 mg "omne in die - once daily" (OD) or nevirapine 200 mg OD for the first 2 weeks and after that 200 mg BID). Efavirenz will be used in all male patients according to national HIV guidelines. Pregnant patients and female patients with a child bearing potential will be treated with nevirapine if CD4+ cell count is ≤ 350 cells/mm3 with close monitoring of liver enzymes during the first 12 weeks in patients with CD4+ cell count >250 cells/mm3. Females beyond childbearing age will be treated with efavirenz.
    Other Names:
    • Stocrin
    • Sustiva
    • Viramune
  • Drug: Ritonavir-boosted lopinavir
    2 NRTIs (lamivudine 150 mg BID and either zidovudine 300 mg BID if hemoglobin is ≥ 8 g/L or stavudine 30 mg BID if hemoglobin is < 8 g/L) and 1 PI (ritonavir-boosted lopinavir 400/100 mg BID).
    Other Names:
    • Kaletra
    • Aluvia
  • Active Comparator: NNRTI
    Intervention: Drug: Efavirenz or Nevirapine
  • Active Comparator: Protease inhibitor
    Intervention: Drug: Ritonavir-boosted lopinavir
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
400
April 2014
April 2014   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Antiretroviral treatment (ART) naïve HIV-1 infected patients. Women receiving ART during pregnancy can be included.
  • Age ≥ 18 years
  • CD4+ cell count ≤ 350 cells/µL and/or
  • Clinical signs of immune suppression (WHO clinical stage 3 or 4) irrespective of CD4+ cell count.

Exclusion Criteria:

  • Tuberculosis (TB) treatment with rifampicin at the time of enrolment.
  • Co-infection with HIV-2.
  • Grade 3 or 4 alanine transaminase (ALAT) elevation (>5 times upper normal limit).
  • Patients with cerebral disturbances that complicates the ability to give informed consent or follow the treatment regime.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Guinea-Bissau
 
NCT01192035
11/CNES/2010
Yes
University of Aarhus
University of Aarhus
  • Aarhus University Hospital Skejby
  • Bandim Health Project
  • Ministry of Health, Guinea-Bissau
  • Abbott
Principal Investigator: Sanne Jespersen, MD Aarhus University Hospital Skejby
Study Director: Alex L Laursen, MD, DMSc Aarhus University Hospital Skejby
Study Director: Lars Oestergaard, Prof MD DMSc Aarhus University Hospital Skejby
Study Chair: Christian Wejse, MD, PhD Aarhus University Hospital Skejby
University of Aarhus
December 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP