Can an extra HIV drug flush out the hidden virus?
NCT ID NCT07193875
First seen Jun 27, 2026 · Last updated Jul 17, 2026 · Updated 1 time
Summary
This completed Phase 4 trial tested whether adding efavirenz (a standard HIV drug) to a person's usual combination therapy could reduce the size of the hidden HIV reservoir. Seven adults with well-controlled HIV took one extra pill daily for six months. Researchers measured safety and checked for changes in the virus's hiding places in blood and tissue.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Efavirenz 600mg
- What this could lead to
- If it works, this could point toward a way to reduce the hidden HIV reservoir, potentially making it easier to control the virus long-term.
- What could go wrong
- This is a very small, early-phase trial with only 7 participants, so results may not apply broadly. Efavirenz can cause side effects like mood changes or rash.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
9 people
The number who actually took part.
- Started
-
Feb 2023
- Finished
-
Dec 2024
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. At least 18 years of age 2. Diagnosis of HIV 3. Documentation of at least two historical HIV-1 RNA viral load measurements \<500 copies/mL while on ART obtained by standard assay. 4. No known non-nucleoside reverse transcriptase inhibitor (NNRTI) resistance mutations. 5. Currently on a stable regimen including an integrase strand transfer inhibitor (INSTI) and two nucleoside reverse transcriptase inhibitors (NRTI). Receiving the current regimen for at least 90 days prior to study entry with no intention to change for the duration of the study. Exclusion Criteria: 1. Untreated depression, defined as a Patient health questionnaire 9 (PHQ-9) score \> 15 at time of enrollment 2. Known prior NNRTI resistance, or INSTI resistance. 3. Cytochrome 450 polymorphism resulting in rapid or delayed metabolism of Efavirenz 4. Not currently on a PI based regimen. 5. Does not have an immunocompromising medical condition. (ie malignancies particularly leukemia, lymphoma, use of immunosuppressive or antineoplastic drugs or X-ray treatment). 6. Chronic, acute, or recurrent infections that are current and serious, in the opinion of the site investigator. 7. Breastfeeding patients as well as those whom are pregnant or plan to become pregnant during period of the study. 8. Those with active Hepatitis C or Hepatitis B.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Washington University in St Louis
St Louis, Missouri, 63110, United States
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