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Last Updated: 02/08/2024

Study of new antimalarial transdermal-drug development

Objectives

*Original title and text were machine translated from Japanese.

By combining selected existing antimalarial drugs with N-89 as a transdermal formulation, this study aims to ultimately optimize a transdermal N-89 combination drug that is sustained release and does not exhibit a first-pass liver effect.

Principal Institution

Okayama University, Japan

Principal Investigators / Focal Persons

Hye-Sook Kim

Rationale and Abstract

Focusing on a transdermal formulation as a new dosage form that can be easily administered to children infected with malaria, the development policy was modified to create a transdermal formulation of N-89, which had already been discovered as a new oral antimalarial drug. Optimization was performed. For clinical use, partner drugs are added to the N-89 formulation, which is made from a base mixture of two types of amphipathic molecules with different molecular weights, Polyethylene Glycol (PEG), which are existing antimalarial drugs with different blood half-lives and structures. Selected from.

Date

Apr 2023 — Mar 2026

Total Project Funding

$34,916

Funding Details
Project Site

Japan

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