
Critical Path Institute
Optimizing drug development through multi-stakeholder collaboration and regulatory science.
Critical Path Institute convenes pharmaceutical, government, patient, and academic organizations to optimize drug and medical product development through collaborative consortia, regulatory science initiatives, and clinical trial design optimization.
Phases
Indications / Therapeutic Areas
Services
About this organization
Critical Path Institute (C-Path) is a non-profit organization that optimizes drug and medical product development lifecycles by convening stakeholders across the pharmaceutical industry, government agencies, patient communities, and academic institutions.
C-Path operates disease-specific and cross-functional consortia that address critical gaps in drug development:
- Critical Path for Alzheimer's Disease — develops tools to optimize clinical trial designs, identify individuals best suited for trials, and define meaningful benefits for early-stage disease.
- Type 1 Diabetes (T1D) Consortium — translates scientific findings into actionable insights for decision-makers advancing therapeutic initiatives.
- Duchenne Regulatory Science Consortium (D-RSC) — focuses on regulatory science and accessibility for Duchenne muscular dystrophy development.
- ALS Research and Clinical Trial Design — addresses fragmented efforts by fostering collaboration among the FDA, NIH, C-Path, and patient advocates.
- CP-RND (Critical Path – Rare & Neglected Diseases) — a collaboration with the FDA and NIH to accelerate development through natural history data collection.
C-Path's mission is to make a difference for patients and their families by bridging communication gaps between scientists, regulators, industry, and patient communities, enabling more efficient and patient-centric drug development.
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