Completed Infection & Immunity

A pipeline of drugs for leishmaniasis and Chagas' disease.

In plain English

AI plain-English summary

Leishmaniasis and Chagas’ disease kill thousands of people each year, yet the drugs available to treat them are outdated, toxic, or failing in clinical trials. A team from GSK and the University of Dundee is now pushing a pipeline of new drug candidates through the final stages of preclinical development, aiming to deliver at least two—and ideally three—preclinical candidates within five years. Current therapies for visceral leishmaniasis (VL), cutaneous leishmaniasis (CL), and Chagas’ disease are not fit for purpose, and recent clinical trials have failed. The field has sparse drug pipelines and general agreement that combination treatments are needed. The GSK/Dundee team has built robust profiling platforms that allow rapid triaging of promising chemical series. They already have a preclinical candidate for VL, a further potential candidate, and have identified the molecular targets of two phenotypic series that showed efficacy in rodent models. If successful, this programme will produce a sustained pipeline of leads and preclinical candidates, including target-based approaches and combination therapies. That could replace the inadequate drugs currently used in some of the world’s poorest regions, where these parasitic diseases cause chronic illness, disability, and death.

View original technical description
Visceral leishmaniasis (VL), cutaneous leishmaniasis (CL) and Chagas’ disease (CD) cause significant morbidity and mortality worldwide. These continuing unmet medicals needs are caused by the current therapies being not fit for purpose, recent clinical trials failures, sparse community pipelines and general agreement that combination treatment is required for these diseases. Our integrated GSK/Dundee team has developed unique and robust profiling platforms to allow rapid triaging of hit series. Today our pipeline is populated with quality assets at all phases, including a preclinical candidate and a further potential candidate for VL. Additionally, we have identified the targets of two phenotypic series with demonstrated efficacy in a VL rodent model.These achievements ensure that we are uniquely positioned to deliver a stretched goal of three, with a minimum of two, preclinical candidates, together with a pipeline of leads for these diseases within the 5 year Programme.The proposed Programme will focus on three main pillars:• Efficient progression of our early-stage pipeline towards preclinical candidates.• Expanded target-based approaches, including targets with demonstrated in vivo efficacy.• Investigation of combination therapies with our current portfolio.Additionally,

View the original record at the funder ↗

Researchers

Paul Wyatt (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Converting natural product leads into structure- and ligand-based drug discovery campaigns against leishmaniasis and Chagas' disease
Developing the first innovative treatments against visceral leishmaniasis
21st Century Treatments for the Sustainable Elimination of Leishmaniasis
Development of a new preclinical candidate for Chagas disease
Development of a preclinical candidate for Chagas disease that acts through inhibition of Trypanosoma cruzi squalene synthase

Original classification

Portfolio Award

Plain English summaries and category classifications on this site are generated by AI and may not perfectly reflect the original research.