Pilot Study of Maraviroc/Raltegravir for Naive HIV-1 Patients

HIV Clinical Trial

— NNNB  

Official title:

Phase II Pilot Study of Simplification to Maraviroc - Raltegravir Dual Therapy After 6 Months of Maraviroc - Raltegravir - Tenofovir - Emtricitabine Quadruple Therapy in ARV Treatment-naive, HIV-1-infected Patients With CCR5- Virus

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT01291459
• Other study ID #: 2009/HD/01
• Status: Active, not recruiting
• Phase: Phase 2
• First received: January 26, 2011
• Last updated: December 29, 2015
• Start date: September 2011
• Est. completion date: December 2015

Study information

• Verified date: December 2015
• Source: Association Pour la Recherche en Infectiologie
• Contact: n/a
• Is FDA regulated: No
• Health authority: France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
• Study type: Interventional

Clinical Trial Summary

Background and Rationale

Raltegravir and Maraviroc, the first in class of 2 new families of antiretroviral drugs have demonstrated a high potency in treatment experienced and naive patients. Both drugs appeared well tolerated with low metabolic toxicity. No data are currently available concerning the combination of these 2 drugs.

Hypothesis

Maraviroc + Raltegravir should be potent enough to maintain virological efficacy in naive patients infected by CCR5 HIV-1 previously treated for 6 months with a Maraviroc-Raltegravir-Tenofovir-Emtricitabine combination.

Description:

Objectives:

• To establish the ability of a Maraviroc-Raltegravir combination to maintain HIV-1 viral load < 50 copies/ml at week 48 in naive patients infected by CCR5 HIV-1, following an initial 6 month phase of Maraviroc-Raltegravir-Tenofovir-Emtricitabine combination (Intent to treat and strategy analysis)

• To study CD4 progression from baseline to week 48

• To study the time to virological failure during the simplification phase of the study (from week 24 to week 48)

• To study the proportion of patients with HIV RNA < 50 copies/ml at each time point

• To study the kinetics of viral load decrease from baseline to week 12

• To study the kinetics of proviral DNA decrease from baseline to week 12, 24, 36 and 48

• To study the clinical and biological tolerance of Maraviroc-Raltegravir combination through week 48

Study Design/ Clinical Plan

Pilot, multicenter, national, uncontrolled study

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 40
• Est. completion date: December 2015
• Est. primary completion date: December 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age = 18 years old at the run-in visit

• HIV-1 infection

• Antiretroviral treatment-naive

• CD4 = 200 /mm3

• HIV- RNA = 1000 copies/ml

• HIV-RNA = 100,000 copies/ml

• Antiretroviral therapy is indicated according to current guidelines

• CCR5-tropic virus according to the Trofile ES® assayGeno2Pheno algorithm using a predefined false positive rate of 20%

• No significant NRTI, NNRTI or PI resistance mutation

• Freely-given, written, informed consent obtained; the patient and investigator have signed the consent form (by the latest on the day of the run-in visit and before performing any examinations required by the trial)

• Patient covered by a French national health insurance scheme

Exclusion Criteria:

• Women of child-bearing potential not using effective contraception (barrier method)

• Pregnant or breast-feeding women

• Patients under the age of 18 years

• Patients deprived of liberty by a judicial or administrative, hospitalized patients without consent, patients admitted to a health or social purposes other than research

• Persons major subject of a measure of legal protection or unable to consent

• Previous antiretroviral therapy (with the exception of post-exposure prophylaxis if HIV serology is negative > 3 months after the last dose of antiretroviral drugs)

• CXCR4-tropic virus, dual/mixed-tropic virus or undetermined tropism on screening

• Presence of significant NRTI, NNRTI or PI resistance mutation(s)

• Infection or co-infection with HIV-2, or group O or N HIV-1

• Acute phase of an opportunistic infection

• Undergoing treatment for tuberculosis

• Undergoing chemotherapy and/or radiotherapy for neoplastic disease

• Decompensated cirrhosis (Child-Pugh class B or C)

• HIV-HBV co-infection. Patients with HIV-HCV co-infection are permitted to participate in the absence of decompensated cirrhosis (Child-Pugh class B or C), of hepatocytolysis > 3 times the upper limit of normal and if treatment for HCV during the ensuing 12 months is not indicated. PAtients with occult HBV are excluded.( positive AcHBc, negative AcHBs, negative AgHBs, positive HBV DNA)

• Co-administration of prohibited treatments (see the SPCs of each product) Laboratory parameters: Haemoglobin < 7g/dl, neutrophil count < 500/mm3, platelet count < 50,000/mm3, creatinine clearance < 50 ml/min, alkaline phosphatase, AST, ALT or bilirubin = 3 times upper limit of normal

• Patient refuses to participate

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• HIV

Intervention

Drug:
• MVC/RAL/FTC/TDF followed by Maraviroc/Raltegravir
MVC/RAL/FTC/TDF 24W followed by MVC/RAL until W48.

Locations

Country	Name	City	State
France	Cannes hosipital	CAnnes
France	CHU	Clermont-Ferrand
France	Frejus hospital	Frejus
France	Croix Rousse hospital	Lyon
France	Edourad Herriot hospital	Lyon
France	Conception hospital	Marseille
France	Ste MArguerite Hospital	MArseille
France	Hotel Dieu hospital	Nantes
France	Hopital l'Archet 1	Nice
France	Pitie Salpetriere Hospital	Paris
France	St Louis Hospital	Paris
France	Nord Hospital	St Etienne

Sponsors (1)

Lead Sponsor	Collaborator
Association Pour la Recherche en Infectiologie

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	HIV-1 viral load	measure of HIV viral load at 48 weeks of treatment for all patients	48 weeks	Yes