Maraviroc Immune Recovery Study (MIRS)

S.F.L. van Lelyveld

Status and phase

Completed

Phase 4

Conditions

HIV Infections

Treatments

Drug: maraviroc

Drug: Placebo

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00875368

08-283

Details and patient eligibility

About

Rationale: Improving cellular immunity by means of increasing CD4 cells is one of the goals of antiretroviral therapy in HIV, which is achieved by means of virological suppression. A certain group of patients, the so called "immunologic non responders", fail to reach an acceptable CD4 cell increase despite an adequate virologic response on antiretroviral treatment. Recently a new antiretroviral agent, maraviroc (Celsentry®), is registered for the treatment of patients infected with CCR5 tropic HIV-1 virus. However, data is available suggesting that treatment with maraviroc leads to immune recovery (increase in CD4 cells) in patients who are infected with dual/mixed tropic HIV-1 virus, in the absence of a virologic response. This suggests an alternative mechanism for immune recovery, which could be especially beneficial for this group of patients.

Hypothesis: Maraviroc, by a yet unknown mechanism, stimulates immune recovery by increasing CD4+ cell count.

Objective: The primary objective is to confirm the hypothesis that maraviroc stimulates immune recovery; the secondary objective is to explore, by virologic and immunologic investigations, the underlying mechanisms of this hypothesis.

Study design: multicentre, randomized, placebo-controlled, double blind, exploratory mechanistic study.

Study population: HIV-1 infected patients 18 years or older, who meet the inclusion criteria.

Intervention: One group receives maraviroc (dose dependent on co-medication), the other group placebo.

Main study parameters/endpoints: A 30% increase in CD4 cell rise in the treatment group (compared with placebo).

Nature and extent of the burden and risks associated with participation, benefit and group relatedness:

In the treatment group subjects will start with a registered antiretroviral agent (maraviroc).
During the treatment year patients will perform several study visits, probably three more compared with regular visits on the outpatient clinic.
Each visit, blood will be drawn by venepuncture for immunologic and virologic investigations (see flow chart).

Enrollment

85 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age 18 years or older
HAART with a maximal treatment interruption of two weeks
viral suppression (< 50 copies/ml) for 6 months
And either:
- CD4+ count < 200 cells/microliter after minimal one year of treatment with HAART (study group one) OR
- a CD4+ cell count between 200 and 350 cells/microliter after minimal two years of treatment with HAART (study group two)

Exclusion criteria

HAART consisting of a combination of tenofovir and didanosine
Active infection for which antimicrobial treatment
Acute hepatitis B or C
Chronic hepatitis B or C for which treatment with (peg)interferon and/or ribavirin (Note: patients with untreated chronic hepatitis B or C can be included)
Immunosuppressive medication
Radiotherapy or chemotherapy in the past 2 years
Pregnancy or breastfeeding an infant
Subjects with known hypersensitivity to maraviroc or to peanuts, or any of its excipients or dyes as follows:
- Excipients from tablet: microcrystalline cellulose, dibasic calcium phosphate (anhydrous), sodium starch glycolate, magnesium stearate.
- Film-coat: [Opadry II Blue (85G20583) contains FD&C blue #2 aluminium lake, soya lecithin, polyethylene glycol (macrogol 3350), polyvinyl alcohol, talc and titanium dioxide.