HIV drug swap proves safe in landmark trial
NCT ID NCT00454337
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether people with HIV who have their virus under control can switch from the injectable drug enfuvirtide to the oral pill raltegravir. 170 participants were randomly assigned to either stay on their current treatment or switch to raltegravir. The goal was to see if the switch was just as good at keeping the virus suppressed. The study found that switching was safe and effective, offering a more convenient treatment option.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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170 people
The number who actually took part.
- Start date
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May 2007
- Finished
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Sep 2008
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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: * Chronic HIV-1 infection * Treatment with a well-tolerated combination of antiretroviral drugs unchanged for at least 3 months, including enfuvirtide * Absence of any uncontrolled opportunistic disease * No restrictions on CD4 lymphocyte levels * Plasma HIV-1 RNA below 400 copies per ml for at least 3 months (at least two consecutive tests below 400 copies per ml prior to inclusion in the study, not including that on W -4) * For women of childbearing age, use of mechanical contraception during any sexual intercourse and negative pregnancy test (plasma ß HCG) at W -4 Exclusion Criteria: * HIV-2 infection * Plasma HIV-1 RNA levels above 400 copies/ml on one occasion during the 3 months prior to screening (or the pre-inclusion visit at W -4) * Poor compliance with antiretroviral therapy current at W -4 * Current treatment with an investigational drug (except cohort ATU) * Patient previously treated with an integrase inhibitor in the context of a clinical study * Woman who is pregnant or likely to become so, is breastfeeding or refuses to use contraception * Multiple drug therapy ongoing or necessary in the foreseeable future for Kaposi's disease or lymphoma * Treatment with interferon ongoing or necessary in the foreseeable future for chronic hepatitis B or C * Acute hepatitis whatever the case, or decompensated cirrhosis * Current treatment with interferon, interleukin or anti-HIV vaccine * Any condition (including, but not limited to, the consumption of alcohol or drugs) which might, in the investigator's opinion, compromise the safety of treatment and/or patient compliance with the protocol * Significant biological abnormalities (hemoglobin below 8g per dl, polynuclear neutrophils below 750 per mm3, platelets below 50,000 per mm3, serum creatinine above 3 times the level deemed normal by the laboratory (N), ASAT or ALAT above 5N, serum lipase above 2N) and total bilirubin above 2N (except if the patient is receiving atazanavir or indinavir) * Concomitant treatments including one or more compounds interacting with UGT1A1 * anti-infective agents: rifampicin/rifampin * psychotropic/anti-epileptic drugs: phenytoin, phenobarbital.
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Genom att skicka in godkänner du våra Användarvillkor
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
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Service des maladies infectieuses et tropicales Hopital Saint Louis
Paris, 75010, France
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