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DORAvirine Versus DOlutegravir Based Antiretroviral Regimens in Treatment-naïve People Living With HIV-1 Infection

Registration Number
NCT06203132
Lead Sponsor
ANRS, Emerging Infectious Diseases
Brief Summary

Phase III trial evaluating doravirine as an alternative to dolutegravir in treatment naïve people living with HIV-1 infection.

Detailed Description

Phase III, multicenter, open-label, randomized, non-inferiority clinical trial which aims to assess the non-inferiority of doravirine in association with tenofovir and lamivudine, as compared to dolutegravir in association with tenofovir and lamivudine or emtricitabine.

This trial will be implemented in Brazil, Cambodia, Cameroon, Côte d'Ivoire, France and Mozambique.

Six hundred and ten patients will be enrolled and followed for 96 weeks after entry in the trial (=ART initiation).

Primary endpoint will assess virological efficacy at Week 48, measured by the proportion of subjects achieving HIV-1 RNA \<50 copies/mL, in HIV-1 infected, treatment-naive subjects with pre-treatment viral load (HIV-1 RNA) ≥ 1,000 copies/mL.

Secondary endpoints are planned at W48 and W96.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
610
Inclusion Criteria
  • Be at least 18 years of age on the day of signing the informed consent.
  • Be HIV-1 positive as determined according to national testing strategies
  • Have a plasma HIV-1 RNA ≥1000 copies/mL within 30 days prior to the randomization,
  • Have HIV treatment indication based on physician assessment according to local treatment guidelines
  • Be naïve to antiretroviral therapy (ART) including investigational antiretroviral agents
  • For women or transgender men of childbearing potential i.e. of childbearing age who are not menopausal, or permanently sterilized (e.g. tubal occlusion, hysterectomy, bilateral salpingectomy) or not refraining from sexual activity: negative urinary test for pregnancy and acceptance to use contraceptive methods
  • Understand the study procedures and voluntarily agree to participate by giving written informed consent for the trial.

Non-inclusion Criteria:

  • Has ongoing (pulmonary or extra-pulmonary) tuberculosis

  • Has any other history or current evidence of any condition, therapy, laboratory abnormality or other circumstance that might confound the results of the study or interfere with the subject's participation for the full duration of the study, such that it is not in the best interest of the subject to participate.

  • Is infected with HIV-2 or co-infected with HIV-1 and HIV-2

  • Has received cabotegravir long acting or dapivirine pre-exposure prophylaxis (PrEP).

  • Has received oral pre-exposure prophylaxis (PrEP) or post-exposure prophylaxis (PEP) in the past three months or has had no negative HIV-1 serology performed

  • Has documented or known resistance or possible resistance to study drugs (in France and where national guidelines recommend screening for primary resistance before starting first-line ART) as defined by the ANRS MIE AC43 Resistance group

  • Has the following laboratory values at screening visit, within 30 days prior to the randomization:

    • AST (SGOT) and ALT (SGPT) >4.0 x upper limit of normal
    • Estimated glomerular filtration rate at time of screening <60 mL/min/1.73m², based on the CKD-EPI equation
  • Has participated in a study with an investigational compound/device within 30 days prior to signing informed consent or anticipates participating in such a study involving an investigational compound/device during the course of this study.

  • Has used systemic immunosuppressive therapy or immune modulators within 30 days prior to treatment in this study or is anticipated to need them during the course of the study

  • Requires or is anticipated to require any of the prohibited or contraindicated medications noted in the trial protocol.

  • Has significant hypersensitivity or other contraindication to any of the components of the study drugs.

  • Is pregnant, breastfeeding, or expecting to conceive at any time during the study.

  • Has any condition which might, in the investigator's opinion, compromise the safety of treatment and/or patient's adherence to study procedure.

  • Is a person under guardianship or deprived of freedom by a judicial or administrative decision

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Exclusion Criteria

Not provided

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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Doravirine armDoravirine + tenofovir DF + lamivudineDoravirine (100 mg) + tenofovir DF (300 mg) + lamivudine (300mg) administered daily
Dolutegravir armDolutegravir + tenofovir DF + lamivudine or emtricitabineDolutegravir (50 mg) + tenofovir DF 300 mg + XTC (300 mg if lamivudine ou 200 mg if emtricitabine) administered daily
Primary Outcome Measures
NameTimeMethod
Non-inferiority of doravirine in combination with tenofovir and lamivudine as compared to dolutegravir in combination with tenofovir and lamivudine or emtricitabineWeek 48

The non-inferiority will be assessed in terms of virologic efficacy at week 48, measured by the proportion of subjects achieving a rate of HIV 1 RNA \<50 copies/mL, in HIV-1 infected, treatment-naive subjects with pre-treatment viral load (HIV-1 RNA) ≥ 1,000 copies/mL.

The rate of HIV 1 RNA will be measured by RT-PCR.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (6)

National Center for HIV/AIDS, Dermatology and STD (NCHADS)

🇰🇭

Phnom Penh, Cambodia

Laboratory on Clinical research on AIDS-INI FIOCRUZ

🇧🇷

Rio De Janeiro, Brazil

Yaoundé Central Hospital

🇨🇲

Yaoundé, Cameroon

SMIT CHU de Treichville, CEPREF, CNTS

🇨🇮

Abidjan, Côte D'Ivoire

Service de Maladies Infectieuses et Tropicales AP-HP Hôpital Saint-Louis-Lariboisière

🇫🇷

Paris, France

Centro de Saúde 1o de Maio

🇲🇿

Maputo, Mozambique

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