Avalanche Biotechnologies, Inc., announced that it has entered into a “definitive agreement” to acquire the French company Annapurna Therapeutics SAS. The merger, expected to close by mid-2016, has been approved by the boards of directors of both companies but is subject to approval by Avalanche stockholders. Under the agreement’s terms, Avalanche will acquire the totality…
Chondrial Therapeutics recently announced that further development of its lead drug candidate for the treatment of Friedreich’s ataxia, TAT-Frataxin (TAT-FXN), will be aided by researchers with the Therapeutics for Rare and Neglected Diseases (TRND) program, run through the National Institutes of Health (NIH), with the aim of filing an Investigational New Drug (IND) application for the therapy and…
Catabasis Pharmaceuticals, Inc., recently announced that it will receive the Kyle Bryant Translational Research Award, given by the Friedreich’s Ataxia Research Alliance (FARA), to further evaluate CAT-4001, a potential Friedreich’s ataxia (FA) drug. CAT-4001 is being developed by Catabasis as a potential treatment for neurodegenerative diseases, such as FA and amyotrophic lateral…
Annapurna Therapeutics has just announced it will collaborate with Weill Cornell Medicine to develop a market-leading partnership specialized in gene therapy. One of these therapies currently under Annapurna’s exclusive development targets cardiomyopathy as it is associated with Friedreich’s ataxia, a disease that affects between 10,000 and 20,000 people in the U.S. and Europe. Friedreich’s ataxia…
Retrotope recently announced a second clinical trial site, the Collaborative Neuroscience Network, LLC (CNS), has opened in Long Beach, California, as part of the company’s ongoing 28-day, first-in-human randomized, double-blind, controlled, ascending dose study of orally dosed experimental therapy RT001. The study will evaluate the safety, tolerability, pharmacokinetics (PK), disease state and exploratory endpoints in…
A team of researchers have identified six new, highly specific compounds that hold promise of bringing “new perspectives” to the treatment of Friedreich’s ataxia (FA). The research, entitled “A Yeast/Drosophila Screen to Identify New Compounds Overcoming Frataxin Deficiency,” was published in Oxidative Medicine and Cellular Longevity. FA is a neuromuscular…
A symposium focused on the rare genetic disease Friedreich’s ataxia, titled, “Understanding Energy for A Cure“, will gather some of the most prominent researchers and disease experts under one roof and help bridge the communication gap between patients and reliable sources of information and updates on FA. The event is hosted by the University…
The Muscular Dystrophy Association (MDA), together with the Friedreich’s Ataxia Research Alliance (FARA), have announced a new strategic partnership geared towards discovering better ways to address Friedreich’s Ataxia (FA) through advancing research, therapeutic development and clinical care. This alliance further strengthens the former’s dedication to forming partnerships both with for- and not-for-profit…
The Muscular Dystrophy Association, the world’s leading nonprofit health agency dedicated to save and improve the lives of people with muscle disease amyotrophic lateral sclerosis (ALS) and other neuromuscular diseases, recently announced it awarded some of the world’s most promising and esteemed scientists research grants amounting to $10 million to fund…
The National Ataxia Foundation, an organization dedicated to improving the lives of those affected by ataxia through support, education and research, is counting down the days to the 16th Annual International Ataxia Awareness Day on September 25, 2015, which will help bring together ataxia organizations from all over the globe in…
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