A drug with the potential to delay the progression of motor neuron disease (MND) could be in human trials within three years.
Associate Professor Trent Woodruff said a private company would undertake formal pre-clinical safety trials with the drug.
“As long as the results from the safety studies are positive, the drug could be ready to be trialled in patients in 2019,” Dr Woodruff said.
“To date we have only tested the drug in one model based on the inherited form of MND, but we believe the same inflammatory pathway is likely to be active in all forms of MND,” Dr Woodruff said.
“Our next project will focus on sporadic MND, which accounts for 90 per cent of patients.”
There is no known cure for MND, a terminal disease with an average life expectancy of two and a half years.
People with MND progressively lose the use of their limbs and ability to speak, swallow and breathe.
“At the moment, the only drug available for patients prolongs survival by two to three months at most,” Dr Lee said.
“In animal models, PMX205 made a visible difference to tremors, muscle strength and mobility, and if this is reflected in people, it could make a real difference to patients.”
The drug has obtained “orphan drug” approval from United States and European licencing authorities, which allows for accelerated progression to human trials.