Status:
RECRUITING
DORAvirine Versus DOlutegravir Based Antiretroviral Regimens in Treatment-naïve People Living With HIV-1 Infection
Lead Sponsor:
ANRS, Emerging Infectious Diseases
Collaborating Sponsors:
MSD France
European and Developing Countries Clinical Trials Partnership (EDCTP)
Conditions:
HIV-1-infection
Eligibility:
All Genders
18+ years
Phase:
PHASE3
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 dolut...
Eligibility Criteria
Inclusion
- 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
Exclusion
Key Trial Info
Start Date :
January 27 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
November 1 2027
Estimated Enrollment :
610 Patients enrolled
Trial Details
Trial ID
NCT06203132
Start Date
January 27 2025
End Date
November 1 2027
Last Update
January 7 2026
Active Locations (19)
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1
Hospital Geral de Nova Iguaçu
Nova Iguaçu, Rio de Janeiro, Brazil, 26030-380
2
Laboratory on Clinical research on AIDS-INI FIOCRUZ
Rio de Janeiro, Rio de Janeiro, Brazil, 21040-900
3
Hôpital Central de Yaoundé
Yaoundé, Cameroon
4
Centre de prise en charge de Recherche et de Formation (CEPREF)
Abidjan, Côte d’Ivoire