If your organization assists those affected by a rare condition or advocates for scientific discoveries, Pairnomix can support your efforts.
What We Do
Pairnomix offers research services to individuals living with a rare disease that is caused by a previously identified genetic mutation. In providing these services, we will create a laboratory model of the individual’s genetic mutation and perform experiments to understand the impact of that genetic mutation on cellular function. We will then test more than 1,300 approved drugs against the modeled mutation for their abilities to reverse the mutation’s functional consequence. Finally, we will provide our findings to the individual’s physician so they can consider these insights. The costs for research services vary by gene and mutation and are determined by the type of scientific work needed for execution.
How Can Pairnomix Help the People My Organization Represents?
There are two primary ways that Pairnomix’s work can benefit the individuals and families your organization represents:
- We can provide our services to the physicians of individuals who are affiliated with your organization. For more information on how we work with individuals and their physicians, please visit our Patients and Families page.
- If you are looking to sponsor research on a particular genetic mutation, we can also work directly with you to provide that service for your community.
Pairnomix has worked with several foundations, including the KCNQ2 Cure Alliance and The Cute Syndrome Foundation, to perform our research services on specific mutations. To read about how Pairnomix has worked with the KCNQ2 Cure Alliance, click here.
Are There Other Ways for My Organization and Pairnomix to Collaborate?
Our company was founded on a passion for advancing knowledge of rare diseases. We are happy to speak with your group’s leadership board or present our data and our process at community meetings. Please don’t hesitate to reach out to us to explore any possible avenue for collaboration.