Impatient for Patients
We’re racing to develop treatments for genetic conditions.
We’re racing to develop treatments for genetic conditions.
Our hub-and-spoke model is designed to unlock speed, precision, and scalability. Teams operate autonomously as individual ‘spokes’, focused on a specific condition or drug candidate, while our central 'hub’ provides clinical, regulatory, and commercial capabilities & expertise.
We partner with leading academic institutions, furthering academic and late-stage clinical research, aiming to bring the most promising advancements to light.
Our decentralized model rethinks what's possible for patients with genetic conditions. We call this The Bridge Way, and it's how we accelerate discovery, reduce the risk of failure, and deliver results.
A focus on genetic conditions provides the clarity we need to target diseases at their source. And we make sure that existing early-stage research doesn’t sit on the shelf by partnering with academic institutions to give promising work a future.
Our model puts agility first, letting us pursue many paths and pivot with purpose. By connecting focused affiliate teams through shared resources and expertise, we move faster and smarter for patients.
Every step we take is designed to maximize impact for people living with genetic conditions. Our model allows us to advance many therapies at once and quickly adapt to focus on the most promising opportunities to provide first-in-class treatments.
If you’re motivated by the chance to develop transformative treatments for people living with genetic conditions and change the industry in the process, we want to hear from you.
Developing bioavailable small molecule inhibitors for people with cancers driven by RAS and PI3Kα.
Developing transformational therapeutics for people with genetic diseases, with a focus on early-stage research and development.
PRESENTATION · Nov 2025 · PDF
PRESENTATION · Nov 2025 · PDF
PRESENTATION · Nov 2025 · PDF
PRESENTATION · Nov 2025 · PDF