Skip to main content

Deep Genomics discovers therapeutic candidate through its AI platform

Deep Genomics, a company specialising in  AI therapeutics, has announced that its artificial intelligence-based drug discovery platform has identified a novel treatment target and corresponding drug candidate for Wilson disease, a rare, serious, and potentially life-threatening genetic disorder.

‘This is an important milestone for patients affected by Wilson disease and it represents a significant advance in the drug discovery community more broadly,’ said Brendan Frey, founder and CEO of Deep Genomics. ‘Within 18 months of initiating our target discovery effort, we identified a genetic mutation that causes the disease, the chemical properties needed in a molecule to target the mutation, and a compound that warrants further investigation. We are delighted to nominate the first ever AI-discovered therapeutic candidate and are eager to move it rapidly into the clinic for the potential benefit of patients.’

Deep Genomics will develop the candidate, DG12P1, for the treatment of patients with Wilson disease who harbor a genetic mutation that impairs the body’s ability to remove copper. Wilson disease affects approximately one in every 30,000 people worldwide and, if left untreated, can cause life-threatening organ damage.

‘Researchers have struggled for two decades, without success, to understand the mechanism of this genetic mutation that causes Wilson disease,’ said Dr Frederick Askari, associate professor and director of the Wilson disease program at the University of Michigan. ‘The clarity that this artificial intelligence platform has brought to the scientific community is astounding and the potential of a therapy that could operate at the genomic level to correct the disease process is exciting. Patients can now have hope that a therapy may be developed that will recapitulate normal gene function and make their copper problems go away.’

Deep Genomics’ AI system scanned over 2,400 diseases and over 100,000 pathogenic mutations while searching for good drug development opportunities. By analyzing hundreds of millions of data points, Deep Genomics’ AI platform was able to predict and confirm the precise disease-causing mechanism of the mutation Met645Arg, one of several genetic mutations that leads to loss of function of the ATP7B copper-binding protein and thereby identify a clear therapeutic target. The AI system was then used to identify 12 lead candidates out of thousands of potential compounds, taking into account in vitro efficacy and toxicity. DG12P1 was designed to correct the exon-skipping mechanism of Met645Arg and, after tolerability experiments, Deep Genomics declared it the ideal candidate to advance toward IND. 

In a subsequent analysis, Deep Genomics’ AI platform was able to rapidly identify two additional mutations that can cause Wilson disease. These potential therapeutic targets are currently being experimentally confirmed.

‘Our expectation is that going forward, Deep Genomics’ platform will enable them to go from known target to first patient dosed in less than half the time of the industry standard, and they may be able to do this even faster with subsequent programs,’ said Dr Arthur Levin, a member of the company’s Strategic Advisory Board. ‘This is truly unprecedented and opens the door to a smarter, faster, and vastly more efficient means of identifying viable drug candidates for a host of diseases. Developing new therapeutics is full of unknowns, but I am certain that we are witnessing a new era of drug discovery.’



Read more about:

Laboratory informatics

Media Partners