Development of new diagnostic tools
For effective control and surveillance of sleeping sickness, new tests are needed. New diagnostic tests should be affordable, implementable with simple protocols at any health structure level requiring minimum training and equipment, allowing its easy execution by any health worker.
They should provide rapid and reliable results with optimal sensitivity and specificity, for an uncontroversial diagnosis of both forms of the disease. This should enable immediate treatment, avoiding cumbersome parasitological examinations.
In addition, the tests should be stable at room temperature, requiring no refrigeration and having a reasonable volume for easy storage and transport.
WHO HAT Specimen Bank
As part of its contribution to support diagnostics research, WHO has set up a HAT specimen bank. This makes biological samples of patients, (including non-infected controls from the same population, and serological suspects of HAT) available to research institutions working for the development of new diagnostic tests. The aim is to provide reference clinical materials to research institutions to develop and evaluate new tests for diagnosis and staging of HAT, appropriate for use in low-income countries. The central repository of the samples is located at the Institut Pasteur of Paris (ICAReB).
- The Human African Trypanosomiasis Specimen Biobank: A Necessary Tool to Support Research of New Diagnostics
Requests of samples should be made to :
Efforts to develop new molecules
A major issue for ensuring sustainability of control continues to be the complexity of current therapies. There is a need to develop a new therapeutic tool which will not require any particular skills or care to administer, with a regimen lasting a few days, making it manageable by peripheral health staff working in rural areas.
Ideally new drugs should be:
- Effective in both forms of the disease and in both stages, making lumbar puncture unnecessary;
- Stable at room temperature;
- Having a reasonable volume for easy transport and storage, allowing the integration of patient management in the regular health system.
- Affordable by national health systems and patients of endemic countries.
An added problem in the research of new molecules is the numerous challenges of conducting clinical trials for HAT in the field. WHO organized an informal consultation to develop a consensus framework for clinical trials, which safeguards quality data and standardizes methods to permit direct comparability of data.
Clinical trials in phase II/III of a new molecule called fexinidazole are ongoing. Fexinidazole is a new molecule, candidate to be used as oral drug in early and late stages of both forms of HAT. Clinical trials in phase II/III of fexinidazole for gambiense HAT have been finished and now, the medicine is under consideration by regulatory agencies. Clinical trials in phase II/III in rhodesiense HAT are planned.
A new oral drug candidate, the acoziborole has shown promising results in pre-clinical and phase I/II clinical studies and it is currently under phase III studies. Acoziborole is an oxaborole, expected to be administered as a single oral dose, for both disease stages, which would dramatically simplify the current treatment.
The Drugs for Neglected Diseases initiative (DNDi) receives funding fromthe Bill and Melinda Gates Foundation and The European & Developing Countries Clinical Trials Partnership (EDCTP) to undertake this clinical development.
The development of drugs for treatment of sleeping sickness: a historical review, by Dietmar Steverding
Fexinidazole – A New Oral Nitroimidazole Drug Candidate Entering Clinical Development for the Treatment of Sleeping Sickness
SCYX-7158, an Orally-Active Benzoxaborole for the Treatment of Stage 2 Human African Trypanosomiasis
- Major advance in sleeping sickness drug made by Glasgow scientists