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About the solution
"Our technology platform allows us to predict therapies with significantly higher accuracy and safety, much faster than conventional approaches. We are changing the whole model”, Tim observed.
The founders decided to create this tech startup when they heard about Matt Might and his son who was diagnosed with a new rare disease called NGLY1 Disorder.
"The medical profession told him there was no hope and no treatment. After reading his personal story in the New Yorker, we contacted him to help find a treatment for his son. Subsequently, we realised Matt and Bertrand were not alone," the CEO described.
The team developed an AI platform, HealNet, that allows a new model for drug discovery to emerge: a model that operates in a faster and more cost-effective way, which improves the chances of clinical success massively.
With the HealNet AI platform, the team plans to deploy it at scale and find cures for 100 rare diseases by 2025. They’re also working on data layer integrations and precision medicine.
"Once AI will be fully integrated, it will automate the structuring and consolidation of facts within medical data, learn from these facts, and apply the knowledge to discover putative therapeutic interventions even before the disease is affecting the individual. The future of medicine is set to be faster, cheaper and far more efficient," he added.
Adapted from: https://bit.ly/2nLGqxl
More info: https://healx.io/
这些解决方案不应包括使用药物,化学品或生物制品(包括食品);创伤性设备;冒犯性的,商业或内在危险的内容。该解决方案未经医学验证。请谨慎进行!如果您有任何疑问,请咨询健康专家。
DISCLAIMER: This story was written by someone who is not the author of the solution, therefore please be advised that, although it was written with the utmost respect for the innovation and the innovator, there can be some incorrect statements. If you find any errors please contact the patient Innovation team via info@patient-innovation.com
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Father creates treatment for his son’s rare disease
CAREGIVING
Cartilage Development Disorder
Neuromuscular Disorders
Cerebral Palsy
here
Treatment/Surgical device
Difficulty walking or moving
Muscle weakness
Muscle cramps or spasms
Difficulty coordinating movements
Stiffness or rigidity (difficulty moving)
Paralysis of the legs and lower body
Limited range of motion
Muscle pain or stiffness
Cognitive impairment
Joint deformity
Seizures
Fatigue
To improve Treatment/Therapy
Caregiving Support
Medical Genetics
Neurology
Pediatrics
United States
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