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The ALS Association Advances Therapeutic Development with $10 Million Contribution to ALS ACT Initiative

October 2, 2014

In a news release today, The ALS Association announced its financial commitment of $10 million to ALS Accelerated Therapeutics (ALS ACT), a new collaborative project that will accelerate development of new treatments for amyotrophic lateral sclerosis. The ALS Association’s funds are being matched by an additional $10 million from The ALS Finding a Cure Foundation.

The ALS Finding a Cure Foundation is led By Peter N. Foss, Lee Rizzuto and Denis Rizzuto. The foundation was created in April of 2014 and is a tribute to Christie Rizzuto, who was diagnosed with ALS five years ago at age 41. Christie is the wife of Denis Rizzuto. This foundation is a part of the Leandro P. Rizzuto Foundation, a private foundation created and funded by Mr. Rizzuto, owner of Conair and Cuisinart.

The project is made possible by the unprecedented outpouring of support from the Ice Bucket Challenge. ALS ACT is one of four major new initiatives by The Association as a direct result of that support.

ALS ACT is a novel academic-foundation-industry partnership to accelerate treatments for people living with ALS. In partnership with the recently formed The ALS Finding a Cure Team, composed of researchers from General Electric (GE) Healthcare and four academic Northeast ALS Consortium (NEALS) sites, ALS ACT will enact a multi-pronged approach to expediting clinical trials in ALS. Merit Cudkowicz, Co-Chair of NEALS and Chief of Neurology and the ALS Program at Massachusetts General Hospital (MGH), notes that these efforts will accelerate diagnosis, speed development of new treatments for people with ALS, and break down road blocks to finding cures for people with ALS”.  Efforts will include the following:

To accelerate research, data and resources from ALS ACT-supported studies will be openly shared with other ALS researchers.

In addition, ALS ACT will strengthen ongoing collaborative efforts in support of clinical trials, including NeuroBANK, a central repository for clinical research data in ALS, and the NEALS Biorepository. Initially established through the TREAT ALS NEALS Clinical Trials Network, NeuroBANK will host, curate, and disseminate proteomic, genomic and clinical data.

Cooperative synergies among the four new initiatives announced today (ALS ACT, New York Genome Centre, The Neuro Collaborative, and Project MinE) will increase the quantity and most importantly the value of data available for ALS research.

The medical team leading the foundation’s efforts includes: Merit Cudkowicz, M.D., MSc, Massachusetts General Hospital; Robert J. Brown, Jr. M.D., D.Phil., University of Massachusetts Stanley H. Appel, M.D., Houston Methodist Hospital System; Clive Svendsen, Ph.D., Cedars-Sinai; Nadeem Ishaque, Ph.D., and Tom Gentile, Senior Vice President General Electric.GE Global Research.

The ALS Association’s Board of Trustees will be meeting in mid-October to discuss and vote on additional funding decisions related to the use of Ice Bucket Challenge donations.




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