Drug intelligence / Profile preview

methotrexate + etoposide + hydroxyurea + teniposide

Development stage
Unknown
Lead developer
Pfizer
Modality
Small Molecules
Administration
Intravenous
01

Overview

This combination therapy consists of four antineoplastic agents: methotrexate, etoposide, hydroxyurea, and teniposide. Each drug has distinct mechanisms of action: - **Methotrexate** is an antimetabolite that inhibits dihydrofolate reductase, thereby blocking DNA synthesis and cell division[4]. - **Etoposide** is a topoisomerase II inhibitor, preventing DNA strand rejoining and resulting in DNA strand breaks[6]. - **Hydroxyurea** is a ribonucleotide reductase inhibitor, reducing the production of DNA building blocks and halting cell cycle progression in the S phase[7]. - **Teniposide** is another topoisomerase II inhibitor with high liposolubility, allowing it to cross the blood-brain barrier and exhibit prolonged activity[1]. This combination is used for its potential synergistic effects in aggressive malignancies, especially where blood-brain barrier penetration is required. There is limited clinical data on this exact combination, but individual components or related combinations (e.g., methotrexate + teniposide) have been investigated in hematologic malignancies and primary CNS lymphoma[1][3]. The rationale for such combinations is to target multiple phases of the cell cycle and different molecular pathways to improve cytotoxic effect and overcome resistance.

02

Targets

DHFR (Dihydrofolate reductase)RNR (Ribonucleotide reductase)TOP2A (DNA topoisomerase II)

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