KENILWORTH, N.J. & MELBOURNE, Australia--(BUSINESS WIRE) March 4, 2020 -- Merck (NYSE: MRK), known as MSD outside the United States and Canada, and the Walter and Eliza Hall Institute of Medical Research in Melbourne, Australia, today announced the publication of research on the discovery of a novel class of candidate antimalarial agents that block multiple stages of the lifecycle of the parasite that causes the disease. Specifically, they identified novel dual inhibitors of plasmepsins IX and X (PMIX and PMX), two proteases that are essential to Plasmodium falciparum, the predominant cause of the most severe form of the disease. The research was published in the latest issue of the peer-reviewed journal Cell Host & Microbe.

“Our goal is to develop new antimalarial treatments that will kill the parasite once it’s present inside the human body, and we’re excited to be working with Merck scientists and other leaders in the field to advance this novel class of compounds that inhibit PMIX and PMX,” said Professor Alan F. Cowman, Ph.D., Deputy Director, Science Strategy, Division of Infectious Diseases and Immune Defence at the Walter and Eliza Hall Institute of Medical Research and study co-author. “With drug resistance a continuing concern in our malaria-endemic world, a drug regimen that could act on novel targets at multiple stages of the malaria parasite’s lifecycle would not only enhance the utility of the regimen but may potentially help eliminate a major cause of malaria in the future.”

“Resistance against existing treatments remains a concern, underscoring the need for new antimalarial drugs with novel mechanisms of action that can be used to treat, eliminate and eradicate malaria,” said Dr David B. Olsen, Distinguished Scientist, Infectious Diseases Discovery, Merck Research Laboratories and study co-author. “We are excited about the potential of novel dual inhibitors of PMIX and PMX as potential drugs for the treatment and prevention of malaria infection.”

Design and results of preclinical research

In the blood, successive broods of malaria-causing parasites grow inside erythrocytes (red blood cells) and destroy them, releasing daughter parasites, called merozoites, that continue the cycle by invading other erythrocytes. Plasmepsins PMIX and PMX are targets in antimalarial drug discovery because they are involved in the process in which the malaria parasite invades erythrocytes and also in egress of the parasite from cells. Inhibiting PMIX and PMX blocks this process, as well as prevents maturation of certain proteins required for replication. Proper functioning of PMX is also required within merozoites to enter fresh erythrocytes.

In this preclinical research, scientists from Merck and the Walter and Eliza Hall Institute of Medical Research and the Swiss Tropical and Public Health Institute in Basel, screened a targeted library of protease inhibitors that kill the P. falciparum parasite. The two most potent in inhibiting the replication of P. falciparum in vitro were administered to mice to determine in vivo activity against P. berghei infection (a parasite that causes malaria in rodents). Although both compounds suppressed P. berghei parasitemia, they did not have desirable pharmacokinetic attributes.

The researchers conducted optimization studies to identify compounds with required drug-like properties, resulting in the identification of WM382, a compound that acts as a dual inhibitor of PMIX and PMX, and inhibits growth of P. falciparum and P. knowlesi, a parasite that causes malaria in humans and other primates. Oral administration of WM382 cured mice of P. berghei and prevented blood infection from the liver. It also was efficacious against P. falciparum asexual infection in humanized mice and prevented transmission to mosquitoes. The ability of WM382 to block transmission is an important attribute for an antimalarial drug as this characteristic could reduce both the incidence and spread of malaria.

The collaborative research was funded in part by the Wellcome Trust (UK), National Health and Medical Research Council (Australia) and the Victorian Government (Australia).

About Malaria

Malaria is one of the most severe public health problems worldwide. According to the US Centers for Disease Control (CDC), it is a leading cause of death and disease in many developing countries, where the groups most affected are young children, who have not yet developed partial immunity to malaria, and pregnant women, whose immunity is decreased by pregnancy. In 2016, malaria caused an estimated 216 million clinical episodes and 445,000 deaths – most of whom were young children in sub-Saharan Africa. An estimated 90% of deaths in 2016 were in the WHO African Region. According to the World Health Organization’s World Malaria Report 2017, nearly half the world’s population lives in areas at risk of malaria transmission in 91 countries and territories. Direct costs of malaria (e.g., illness, treatment, premature death) have been estimated to be at least $12 billion per year.

About the Walter and Eliza Hall Institute of Medical Research

The Institute is one of Australia’s leading biomedical research organisations, with a national and international reputation for performing highly influential basic and translational research. We are addressing some of the major health challenges of our time, with a focus on cancer, immune health and infection, and development and ageing. We are at the forefront of research innovation, with a strong commitment to excellence and investment in research computing, advanced technologies and developing new medicines and diagnostics. For more information, visit https://www.wehi.edu.au.

Merck’s commitment to infectious diseases

For more than 80 years, Merck has contributed to the discovery and development of novel medicines and vaccines to combat infectious diseases. In addition to a combined portfolio of antibiotic and antifungal and antiviral medicines and vaccines, Merck has multiple programs that span discovery through late-stage development including four programs in Phase 2/Phase 3 clinical trials for the potential treatment or prevention of infectious diseases. (Article from : www.drugs.com)