Drug intelligence / Profile preview

hydroxychloroquine + lopinavir + ritonavir + azithromycin

Development stage
Discontinued
Lead developer
BioXcellerator
Modality
Small Molecules
Administration
Oral
01

Overview

This entry refers to the multi-drug standard therapy regimen used as a comparator arm in a Phase 1/2 clinical trial (NCT04444271) conducted by BioXcellerator for the treatment of COVID-19-associated acute respiratory distress syndrome (ARDS). The regimen consists of hydroxychloroquine (an antimalarial and immunomodulator), the protease inhibitor combination lopinavir/ritonavir, or the macrolide antibiotic azithromycin. These agents were repurposed early in the pandemic for their potential antiviral and anti-inflammatory properties; hydroxychloroquine was thought to inhibit viral entry and Toll-like receptor signaling, while lopinavir/ritonavir was intended to target the SARS-CoV-2 3C-like proteinase (3CLpro). Azithromycin was included for its potential synergistic immunomodulatory effects. In the BioXcellerator trial context, this standard therapy was compared against or combined with Wharton's Jelly-derived Mesenchymal Stem Cells (WJ-MSCs) to evaluate safety and efficacy in critically ill patients.

Other names
Standard Therapy (BioXcellerator COVID-19 Trial)
02

Targets

TLR7 (Toll-like receptor 7)CYP3A4 (Cytochrome P450 3A4)Mpro (3C-like proteinase of SARS-CoV-2)TLR9 (Toll-like receptor 9)Bacterial 50S ribosomal subunitPR (Progesterone receptor)

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