Phase 3
N=184
Impact of a Dolutegravir-based Regimen on Early Mortality of AIDS Patients
Severely Immunocompromised HIV Patients
Bottom Line
View on ClinicalTrials.gov: NCT01837277 ↗Enrolled (actual)
184
Serious AEs
12.0%
Results posted
Dec 2023
Primary outcome: Primary: Early Mortality — 9; 13 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 3
- Interventions
- Dolutegravir 50 mg (Drug); Efavirenz-based regimens (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Fundação Bahiana de Infectologia
- Primary completion
- Jul 2021
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Early Mortality |
9; 13 | — |
| SECONDARY Viral Load |
— | — |
| SECONDARY CD4 Count |
— | — |
Summary
The current available antiretroviral (ARV) agents make possible a successful treatment of virtually all HIV-infected patients, but some problems related to early mortality are still of concern, mainly in resources-limited settings. There are several published reports showing that such patients are at a significantly higher risk of death during the first months of treatment, in comparison with the observed outcomes in developed countries. One of the consistently detected risks for early mortality across these reports is the baseline low CD4 count, although it does not seem to be the only reason for such outcome. In Brazil and other developing countries, there is still a large proportion of AIDS patients who are diagnosed with AIDS, or only seek health care for HIV infection late in the course of disease. Dolutegravir (DTG), the first HIV-1 integrase inhibitor, is a potent and safe ARV drug. The available evidence suggest it promotes a faster decline in HIV-1 plasma viremia, and a higher increase in CD4 cells count, in comparison with those in Efavirenz (EFV) arm. The investigators propose to compare the impact of DTG versus EFV in the early mortality rates for severely ill (CD4+ cells count <50 cells/mm3) patients starting ARV therapy.
Eligibility Criteria
Inclusion Criteria
- Patients with confirmed HIV-1 infection (positive Western blot or plasma HIV-1 RNA >1,000 copies/ml)
- No previous use of any ARV drug (drug-naïve patients)
- Presence of clinical symptoms according to Rio de Janeiro / Caracas´ AIDS definition (Asthenia, Cachexia/Wasting, Cough, Dermatitis, persistent, Diarrhea, Fever, Lymphadenopathy, Candidiasis, oral, or hairy leukoplasia, Central nervous system dysfunction, Herpes zoster in individual younger than 60 years of age)), and/or any active AIDS-defining condition
- Baseline CD4+ cells count equal or lower than 50 cells/mm3
- Age equal or higher than 18 years
- HIV-1 plasma viral load ≥ 1, 000 copies of HIV-1 RNA/ml
Exclusion Criteria
- Undetectable plasma viral load at screening
- CD4 cells count>50 cells/mm3
- Asymptomatic individuals
Data sourced from ClinicalTrials.gov (NCT01837277). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.