Whatever it is, the way you tell your story online can make all the difference.
 
 

The Orphan Disease Center's JumpStart program serves to establish and progress research agendas in emerging and neglected rare diseases. The JumpStart program works closely with patient groups and foundations, pharma and biotech, and the academic community to drive therapeutic development for rare diseases.

The JumpStart program connects patients and foundations to researchers and key opinion leaders, encouraging scientific collaboration. We can provide guidance on developing research tools, such as cell lines and animal models, and we can provide essential guidance on clinical development programs including registry and natural history development.  We also offer assistance organizing symposia and Think Tanks, bringing together KOLs, experts and potential sponsors, and we  can assist rare disease organizations assemble a research grant program, by providing information on best practices.

The JumpStart program offers a tailor approach to disease groups with limited expertise and resources. We can help you overcome obstacles to progress research and bridge gaps for future success.

Due to limited resources, ODC is unable to provide financial support and we offer primarily scientific advisement and network outreach.

 

If you are a parent, patient group, or foundation focused on facilitating research for a rare disease, please email Debbie Requesens to find out more.

 

JumpStart Partners

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Partner With Us

JumpStart Symposia

JumpStart Resources

JumpStart Grants