Molecular Partners: Pioneering Targeted Radiopharmaceuticals
Founded in 2004 as a spin-off from the University of Zurich, Molecular Partners, a Roadshow Partner of Venture Leaders Biotech, has spent two decades developing...
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Meet Kelvin Stott, Co-Founder of Amporin. The biotech startup is developing a new class of small-molecule drugs to stop and reverse degenerative diseases. In June, Kelvin will join nine other Biotech innovators on a business development and investor roadshow in Boston.
Name: Kelvin Stott
Location: Basel, Switzerland
Nationality: British
Graduated from: University of Sussex (BSc), University of Cambridge (PhD)
Job title: CEO & Co-Founder
Number of employees: 3 cofounders
Money raised: CHF 350K—CHF 100K founders' equity + CHF 250K in convertible loans from Venture Kick & Kickfund
Can you tell us who your product or solution helps, and how?
At Amporin, we are developing a breakthrough new class of drugs that could potentially stop and even reverse the progression of more than 50 deadly degenerative diseases associated with protein misfolding and aggregation. Together these diseases affect over half a billion people and kill 3.6 million people around the world each year. Our products could potentially help these people to recover from disease and remain independent for much longer, without the need for years of full-time care.
What market are you addressing and what is the potential of your startup in that market?
Ultimately, we plan to develop the first safe and effective disease-modifying drugs for 6 major degenerative diseases based on our technology, including Alzheimer’s disease and type II diabetes, though we are initially targeting Parkinson’s disease and ALS. Currently, there are no safe and effective disease-modifying treatments for any of these diseases, so our products could help to significantly reduce the CHF 3 trillion in associated healthcare and economic costs each year.
How and where did you come up with the idea for your startup?
I created my first biotech startup to tackle these diseases over 20 years ago, based on my PhD research at Cambridge, but our understanding of these diseases was very limited at the time. Now we have a much better understanding of the underlying disease biology, but this has still not delivered any effective treatments. Frustrated by this, I designed a new class of molecules to target a different form of the misfolded proteins, and these showed potential for acute disease reversal for the very first time.
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