An African solution to save lives
Dr Max Price, the Vice-Chancellor of UCT, said: “H3-D was founded at UCT in 2010 for this very purpose: to develop African expertise towards solving the health problems that beset the developing world. We trust this clinical candidate is the first of many contributions Professor Chibale and his team will be making to the advancement of international medicine.”
H3-D identified a molecule, code named MMV390048, which was selected in July 2012 by MMV’s Expert Scientific Advisory Committee for further development. The promising new compound shows potent activity against multiple points in the malaria parasite’s lifecycle. This means it not only has the potential to become part of a single-dose cure for malaria but might also be able to block transmission of the parasite from person to person.
The aminopyridine series was initially identified by Griffith University scientists in Australia as part of MMV’s extensive malaria screening campaign of around 6 million compounds. A team of scientists from H3-D, led by UCT Professor Kelly Chibale, further scrutinised and explored the antimalarial potential of the series. With parasitological, pharmacological and contract chemistry support from the Swiss Tropical and Public Health Institute (Switzerland), the Centre for Drug Candidate Optimization at Monash University (Australia) and Syngene (India) respectively, the H3-D team selected the most promising compounds from the series to be optimised and retested. In just 18 months the team had identified and developed a candidate suitable for preclinical development.
Equipping the next generation of African scientists
“We are very excited that this promising compound, researched by African scientists, has been selected by MMV for further development,” said Professor Chibale, the Founder and Director of H3-D. “This is truly a proud day for African science and African scientists. Our team is hopeful that the compound will emerge from rigorous testing as an extremely effective medicine for malaria – a disease that accounts for 24% of total child deaths in sub-Saharan Africa. What is more, H3-D and MMV achieved MMV390048 as a clinical candidate in record time. In the process we have developed a unique model for successful technology platforms, and generic modern pharmaceutical industry expertise and skills, to discover drugs in potentially any disease area in Africa.”
Dr Tim Wells, MMV’s Chief Scientific Officer, said: “This is a great achievement and an excellent example of the quality of research that can be fostered in Africa. We look forward to seeing more exciting compounds emerge from Kelly’s team and are proud to be collaborating with H3-D; not only is it conducting excellent science today, but it is also providing world-class training for the next generation of African scientists.”
What is so unique and exciting about MMV390048
It is very potent: it displayed a complete cure of animals infected with malaria parasites in a single dose given orally, and thus has the potential to cure millions of people.
It is active against a wide panel of resistant strains of the malaria parasite.
Developing the drug has made possible the training of more than 10 local scientists and cemented a strong relationship with an international partner.
Article
Murray, C. et al. (2012) Global malaria mortality between 1980 and 2010: a systematic analysis. Lancet 379, 413–431