Drug intelligence / Profile preview

didanosine + stavudine + nevirapine + emivirine + hydroxyurea

Development stage
Preclinical
Lead developer
National Cancer Institute
Modality
Small Molecules
Administration
Oral
01

Overview

This drug is a **five-drug combination therapy** consisting of didanosine, stavudine, nevirapine, emivirine, and hydroxyurea, used experimentally for the treatment of HIV infection. - **Didanosine**, **stavudine**: nucleoside reverse transcriptase inhibitors (NRTIs) that block viral reverse transcriptase, inhibiting HIV replication. - **Nevirapine** and **emivirine**: non-nucleoside reverse transcriptase inhibitors (NNRTIs) targeting HIV-1 reverse transcriptase by binding directly and causing disruption of enzyme activity. - **Hydroxyurea**: a cytostatic agent that can potentiate the antiviral activity of didanosine and possibly stavudine; it acts by inhibiting ribonucleotide reductase, affecting DNA synthesis. This combination has been explored in clinical studies for its potential to intensify antiretroviral therapy and modulate immune response in HIV-infected individuals, especially those with previous antiretroviral exposure. Side effects reported with similar combinations include neutropenia, pancreatitis, and peripheral neuropathy, with close monitoring recommended[1][2]. Emivirine is a non-nucleoside reverse transcriptase inhibitor and has primarily been investigated in research settings for HIV.

02

Targets

Human immunodeficiency virus type 1 reverse transcriptaseRNR (Ribonucleotide reductase)

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