Stay tuned: New clinical trials will be enrolling soon!
It is an exciting time in HD Research! Researchers worldwide have been working diligently to bring more clinical trials than ever before to the HD community.
While this is not a complete list of all the HD research studies that are being planned for 2007, we are able to provide the following information:
IN NORTH AMERICA
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2CARE
More information about the large, Coenzyme Q10 study is expected shortly. Plans are underway to start the 2CARE study in 2007. The latest information from the study's steering committee can be found on the Huntington Study Group web site. Merit Cudkowicz, MD, is the Principal Investigator.
- CREST-E
A trial to test creatine’s safety, tolerability and efficacy in persons with early HD is in the planning stages. The study is currently seeking funding. Steven Hersch, MD, PhD, is the Principal Investigator.
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CYTE-HD II
A trial to test cysteamine's safety, tolerability and efficacy in persons with HD is in the planning stages. The study is currently seeking funding and FDA approval. Richard Dubinsky, MD, is the Principal Investigator.
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PRECREST
The planning of a study to examine safety, tolerability, and biomarkers in individuals at risk for HD treated with creatine is currently underway. Steven Hersch, MD, PhD, is the Principal Investigator.
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PREQUEL
The planning of a trial to test Coenzyme Q10 in pre-manifest HD gene carriers is currently underway. Chris Ross, MD, PhD is the Principal Investigator.
IN EUROPE
Initiating a clinical trial is a timely and multi-stepped process. Two of the most important steps, securing funding and obtaining approval from regulatory and patient protection agencies, can take anywhere from 6 to 24 months to complete. Until these two steps are complete, a study cannot begin.
Below is an overview of the current state of HD research:
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Small, pilot studies are being conducted to assess whether a specific study drug has an effect on HD symptoms. The results of these studies will help to determine if a larger scale clinical trial of the drug is worth pursuing.
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New projects to determine the safety and tolerability of potential study drugs have been proposed by groups working in collaboration with the Huntington Project. These projects are now being reviewed by the FDA. Once the FDA is assured that a study under review will not pose significant harm to the participant, approval to initiate the trials will be granted and enrollment can begin.
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Larger scale studies are awaiting approval from the FDA. These are studies where funding for the study has been secured, however, full regulatory approval from the FDA has not yet been obtained. Huntington Project collaborators continue to meet with the FDA and the funding sources to finalize the regulatory process and get approval to begin these studies.
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The Huntington Project is working in collaboration with our European colleagues, the European HD Network (EHDN) to collaboratively plan and implement collection of natural history data and samples for potential biomarker studies.
The Huntington Project will keep you informed about the latest enrolling HD clinical trials in the coming months. Please continue to check the Currently Enrolling page. New studies will be listed as soon as they are accepting participants.
If you are new to clinical trials, we suggest that you speak with your healthcare providers, family members, or friends who may be able to provide you with information and guidance about participating in a study. For more information about clinical trials for Huntington’s disease, see our Overview page.
The Huntington Study Group may have a research site in your area. Please see Huntington Study Group/HSG Research Sites for contact information. The HSG sites give you access to physicians, nurses, social workers, neuropsychologists and other professionals who specialize in treating Huntington’s disease.
The above trial information was posted in January 2007 and may change at any time.
Please check back for updates. Thank you.