Completed Infection & Immunity Digestion, Kidneys & Other Organs

MICA: Pre-Clinical Development of a Small Molecule anti-Wolbachia Candidate Macrofilaricide Drug

In plain English

AI plain-English summary

More than 157 million people worldwide are disabled by elephantiasis or river blindness, yet no safe drug exists to kill the adult parasitic worms that cause these diseases. The problem is that current treatments target the larval stage of the worms, not the adults. A drug called doxycycline can kill adult worms by attacking the *Wolbachia* bacteria living inside them, but the treatment takes weeks and is unsafe for pregnant women and children. This project has already identified a new compound, AWZ1066S, that kills *Wolbachia* more effectively than doxycycline in animal models and meets all safety requirements for further testing. The researchers now need funding to run the formal pre-clinical safety and manufacturing studies required before the drug can be tested in humans for the first time. If this succeeds, AWZ1066S could become the first safe, short-course oral treatment that kills adult filarial worms. That would transform control programmes for elephantiasis and river blindness, potentially eliminating the need for decades of annual mass drug distribution. For the 157 million people at risk, this would mean a genuine cure rather than just managing symptoms.

View original technical description
Lymphatic filariasis (elephantiasis) and onchocerciasis (river blindness) are two important neglected tropical diseases that cause severe disability and affect more than 157 million people globally. Control efforts are hindered by the lack of a safe macrofilaricidal (adult parasite killing) drug. Targeting the Wolbachia bacterial endosymbionts in these parasites with doxycycline leads to a macrofilaricidal outcome, but protracted treatment regimens and contraindications restrict its widespread implementation. As part of an ongoing macrofilaricide drug discovery project we have successfully completed a lead optimisation programme to deliver a pre-clinical candidate anti-Wolbachia based macrofilaricide. The candidate AWZ1066S shows superior efficacy compared to doxycycline in a range of validated animal infection models, meets all current Target Candidate Profile characteristics (including extensive non-GLP safety/pharmacology and DMPK evaluation) and is positioned for onward development. We now request funding to support the critical formal pre-clinical development programme in order to progress AWZ1066S to the first into man transition.

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Researchers

Joseph Turner (Co-Investigator)Mark Taylor (Co-Investigator)Paul ONeill (Co-Investigator)Stephen Ward (Principal Investigator)

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Research Grant

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