Drug intelligence / Profile preview

raltegravir + maraviroc + efineptakin alfa

Development stage
Unknown
Lead developer
Objectif Recherche Vaccins SIDA
Modality
Cytokines & Interferons → Recombinant Proteins and Enzymes, Small Molecules
Administration
Oral, Subcutaneous
01

Overview

This combination therapy, evaluated in the ERAMUNE-01 clinical trial, consists of antiretroviral therapy (ART) intensification using raltegravir and maraviroc, paired with the immunomodulatory agent efineptakin alfa (recombinant human interleukin-7). Raltegravir is an HIV-1 integrase strand transfer inhibitor that prevents the integration of viral DNA into the host genome, while maraviroc is a CCR5 co-receptor antagonist that blocks viral entry into CD4+ T-cells. Efineptakin alfa (CYT107) is a cytokine that stimulates the expansion and survival of T-cells. The strategy was developed by the non-profit organization Objectif Recherche VACcin Sida (ORVACS) to target the latent HIV-1 reservoir in patients with long-term viral suppression, aiming to reduce the pool of infected cells that persist despite standard ART.

Brand names
IsentressSelzentry
Other names
ART intensification + IL-7r-hIL-7r-hIL7r-hIL 7recombinant human interleukin-7CYT107 + raltegravir + maravirocERAMUNE-01 interventionERAMUNE01 interventionERAMUNE 01 intervention
02

Targets

IL7R (Interleukin-7 Receptor)CCR5 (C-C chemokine receptor type 5)Integrase allosteric pocket (HIV)

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