Critical Path Institute Takes the Lead in Accelerating Drug Development for Mitochondrial and Inherited Metabolic Diseases with New Task Force

C-Path has initiated a task force dedicated to accelerating drug development for mitochondrial and inherited metabolic diseases. Leveraging their demonstrated expertise, particularly in rare and pediatric indications, C-Path aims to utilize the Rare Disease Cures Accelerator-Data and Analytics Platform (RDCA-DAP®) to integrate diverse patient-level data sources.

This collaborative effort provides a neutral environment for industry, regulatory agencies, academia, and the patient community to actively contribute to advancing solutions and facilitating therapeutic developments for these specific medical conditions.

Previous
Previous

Loss of Tax Incentive for R&D Threatens Biotech Innovation

Next
Next

ARPA-H Celebrates Official Launch of Investor Catalyst Hub