The Buffalo Initiative was founded when a group of patient leaders with decades of combined experience in law, business and philanthropy, in addition to running their own disease foundations, came together to create a viable path forward for patient-centered drug development.
At the Buffalo Initiative, we do not accept what is standing in the way of finding treatments for millions of children suffering from genetic brain diseases -- a lack of investment, incentive and coordination to address the issues that matter most to families. This is why we are forming a multi-stakeholder collaborative focused on creating a more equitable and productive clinical research ecosystem that is driven by patient-led research organizations.
Harvest, measure, and evaluate learnings that extend beyond individual data collection efforts.
Adopt open science principles and share knowledge via data, publications & convenings.
Leverage IP ownership to sustain cure-funding
and ensure community control.
We are launching a pilot in 2025 to fund five patient-led research organizations who have advanced preclinical therapeutics for pediatric-onset genetic brain diseases to get to first-in-human clinical trials.
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