At Modelis, we aim at providing a fast and cost effective solution to find a cure for any rare genetic disease. Let us help you be a driving force behind medical research. We understand that drug discovery can feel inaccessible to families, which is why we actively bridge the gap between bench and bedside to accelerate drug discovery for your particular disease.
Our families become genetic avatars and partners that are an essential part of finding a cure to help others living with their rare genetic disease.
OUR FAMILIES BECOME VENTURE PHILANTHROPISTS
What is venture philanthropy? Our families become financially invested in their drug discovery project, which is why we believe that they should share in the upside of any successful clinical trial.
Visit our FAQ page to learn more about starting a project.
HOW WE WORK WITH FAMILIES
We bridge the gap from bench-to-bedside, supporting our families each step of the way throughout the drug discovery process.
You contact us regarding a specific genetic disease
We analyze the feasibility of the project in regard to the gene of interest and the available tools
We develop a research plan and a drug discovery strategy that we validate with you
We start our drug screen pipeline focusing on the cause you hold dear
THE ADVANTAGES OF WORKING WITH US
We mimic the genetic mutations so that we can rapidly test multiple treatments that are customized to the individual. Modelis works alongside you each step of the way making you a key part of our research model.
Taking advantage of simple animal models that cost up to 10x less than classical mammals, our drug discovery pipeline is time and money-efficient.
The Modelis Hub Model
Modelis’ Hub approach brings multiple stakeholders around the table to further support our patient partners throughout the drug discovery process.
How can we help you?
Contact us to learn more about how Modelis serves our families.
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