WHAT WE DO

 

 

We focus on taking drugs or clinical compounds that were created for other indications and repositioning them for use in epilepsy. Several of the  current AEDs have been found in this way (eg. the benzodiazapines).

There are logistical problems with repurposing drugs. A big hurdle is that the drug is owned by a company that might not have the expertise to pursue epilepsy as an indication. In that situation, there are several possible paths forward, including:

  1. Convincing the company that refractory epilepsy is a viable indication
  2. Out-licensing the drug to another company that is willing to pursue it for use in epilepsy.
  3. Collaborating with an academic clinical group to test the drug

In general, these paths are not viable without internal advocates for epilepsy that can champion the drug from within the company. Often, the internal advocate will need support from people with different areas of expertise. Therefore, we are striving to identify people with a large variety of areas of expertise that would be able to provide the support needed to push a drug repurposing effort forward.

 

 

 

WHO WE ARE

 

 

We are a group of people with experience in the discovery and development of new drugs and have a strong desire to identify new AEDs. The network includes individuals in academia, government, the pharmaceutical industry, non-profit epilepsy research foundations, patient advocacy groups, entrepreneurs, venture capital, etc.

Network Members

We are a group of people with experience in the discovery and development of new drugs and have a strong desire to identify new AEDs. The network includes individuals in academia, government, the pharmaceutical industry, non-profit epilepsy research foundations, patient advocacy groups, entrepreneurs, venture capital, etc.

Leadership team

John R. Somoza, Ph.D.

John is the founder of the Translational Epilepsy Foundation and has a daughter with refractory epilepsy. John has 20+ years of experience in drug discovery within the pharmaceutical industry. He has led teams in virology, cancer and fibrosis, and spearheaded the out-licensing of two compounds that show promise for the treatment of epilepsy.

Sharmila Rajan, M.S.

Sharmila has a daughter with refractory epilepsy. She has 17 years of experience in the biotech industry working in the area of in vivo pharmacology supporting a number of therapeutic areas.

Melanie Huntley, Ph.D.

Melanie has a daughter with Lennox-Gastaut Syndrome. She is the president of the LGS Foundation and has 11 years of experience in the biotech industry, where she works in bioinformatics and computational biology.

Advisory board

Daniel Lowenstein, M.D.

Executive Vice Chancellor and Provost at the University of California, San Francisco (UCSF), and the Robert B. and Ellinor Aird Professor and Vice Chairman in the Department of Neurology at UCSF. Dr. Lowenstein is a past president of the American Epilepsy Society.

Laura S. Lubbers, Ph.D.

Chief Scientific Officer of Citizens United for Research in Epilepsy (CURE)

Kiran Reddy, M.D., MBA

President and CEO of Praxis Precision Medicines, a company that focuses on genetically defined neurodevelopmental disorders. Dr. Reddy is also a Venture Partner at Clarus Ventures.

Miguel Stevens, MPharm, Ph.D., MBA

VP, Head of Global Business Development at UCB