Switching from enfuvirtide to raltegravir in the treatment of HIV-infected patients who sustain viral suppression with a combination therapy including enfuvirtide (or : with an enfuvirtide-based combination therapy)

Condition	Intervention	Phase
HIV Infections	Drug: Enfuvirtide  Drug: Raltegravir	Phase III

Further study details as provided by French National Agency for Research on AIDS and Viral Hepatitis:

Primary Outcome Measures: 

• comparison of the proportions of virologic failure, defined as two consecutive pVL above 400 cp per ml, through 24 weeks in enfuvirtide-maintained arm versus raltegravir arm

Secondary Outcome Measures: 

• comparison of time to onset of virologic failure ;
• proportions of pts with pVL under 50 and 400 cp per ml respectively at week 24 and week 48 ;
• plasma viral mutations in the event of virologic failure, compared to HIV-DNA archived mutations at baseline;
• change in CD4 levels;
• incidence of HIV-related events;
• drug plasma and male genital tract pharmacokinetics;
• incidence and type of adverse events, including adverse reactions ;
• proportions of discontinuing allocated treatment strategy ;
• quality of life and adherence ;
• morphological and metabolic disorders outcome.

Total Enrollment:  170

In patients who have failed under the three main classes of antiretroviral agents (NRTI, NNRTI and PI) and in whom the control of viral replication in the plasma has ultimately been achieved with enfuvirtide, the aim is to sustain this virological success for as long as possible to thus enable satisfactory immune reconstitution, avoid further accumulation of viral mutations conferring resistance to the drugs and protect the patient from the risk of opportunistic disease and death.

Indeed, enfuvirtide is the lead compound in the new class of antiretroviral drugs which inhibit the fusion of HIV-1 virus with its target cell. Its in vivo efficacy was demonstrated during the pivotal studies TORO 1 and 2. Despite its efficacy, maintaining long-term treatment with enfuvirtide is nonetheless difficult for patients because of the constraints related to twice-daily subcutaneous parenteral injections. Furthermore, these subcutaneous injections are associated with inflammatory reactions at the injection site in 98 per cent of patients, without any reduction in frequency or severity over time. It is thus critical for patients who are well controlled by enfuvirtide to be able to simplify their treatment by replacing enfuvirtide with another active compound taken by mouth, which would enable maintenance of the virological response and acceptable safety in patients who have usually failed under the three main classes of antiretroviral drugs. A new antiviral compound, viral integrase inhibitor called raltegravir, could be proposed instead of enfuvirtide.

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Criteria

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.

Please refer to this study by ClinicalTrials.gov identifier  NCT00454337

Isabelle Fournier, MD      +33 1 45 59  Ext. 5171    i.fournier@...

France
      Service des maladies infectieuses et tropicales Hopital Saint Louis, Paris,  75010,  France

Study chairs or principal investigators

Nathalie De Castro, MD,  Principal Investigator,  AP-HP Hopital Saint Louis Paris   
Jean M Molina, MD,  Principal Investigator,  AP-HP Hopital saint Louis Paris