C-Path’s Parkinson’s Consortium Supports Groundbreaking Research Utilizing Smartwatches to Monitor Disease Progression

TUCSON, Ariz., June 12, 2024 — Critical Path Institute (C-Path) today announced a new publication on how the use of wearable technology can optimize measuring symptoms important to people with Parkinson’s disease. The newly published manuscript in npj Parkinson’s Disease highlights a multistakeholder initiative consisting of collaborators from around the world coming together to share knowledge, data and resources to ask how new technologies can help to monitor people living with Parkinson’s in new ways.

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C-Path’s AI Collaborations Accelerate Drug Development, Improve Lives 

TUCSON, Ariz., June 12, 2024 — Critical Path Institute (C-Path) today announced the publication of a new peer-reviewed paper in the journal Clinical and Translational Science. As the preeminent leader in public-private partnerships to accelerate drug development, the paper highlights how C-Path’s AI collaborations are revolutionizing drug development, with specific advancements in the management and treatment of Type 1 Diabetes (T1D) and Parkinson’s Disease (PD). This study affirms the Institute’s commitment to using artificial intelligence (AI) and digital health technologies (DHTs) to expedite the delivery of life-saving treatments.

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C-Path Appoints Dr. Amanda Klein as Executive Director for CPLD and CPA-1 Consortia

TUCSON, Ariz., April 17, 2024 — Critical Path Institute (C-Path) today announced the appointment of Amanda Klein, Pharm.D., as Executive Director for its two newest public-private partnerships: the Critical Path for Lysosomal Diseases (CPLD) and the Critical Path for Alpha-1 Antitrypsin Deficiency (CPA-1) consortia . Klein brings a wealth of experience, having previously served as Executive Director of C-Path’s Transplant Therapeutics Consortium (TTC), where she orchestrated successful composite biomarker qualification submissions with the U.S. Food and Drug Administration (FDA) and European Medicines Agency.Continue reading

C-Path Launches Clinical Trial Simulator for Duchenne Muscular Dystrophy Research

TUCSON, Ariz., March 28, 2024 — Critical Path Institute’s (C-Path) Duchenne Regulatory Science Consortium (D-RSC) is excited to announce the launch of a groundbreaking model-based Clinical Trial Simulator (CTS), specifically designed to improve design of efficacy studies for potential therapies for Duchenne muscular dystrophy (DMD). This pioneering Drug Development Tool is set to positively impact the medical research community by significantly optimizing clinical trial design.Continue reading