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DART Therapeutics Initiates Study of HT-100 For Duchenne Muscular Dystrophy
Date:7/15/2013

lure in their late twenties or early thirties. HT-100 may help promote healthy muscle regeneration, reduce inflammation and the resulting damage to muscle, and decrease the scar tissue that forms in the muscles of boys with DMD. The drug candidate has Orphan Drug Status in the U.S. and EU.

The study sponsor, Halo Therapeutics, is a subsidiary of DART Therapeutics. More information is available at clinicaltrials.gov, identifier NCT01847573 or via the following link: http://www.clinicaltrials.gov/ct2/show/NCT01847573.

About DART Therapeutics

DART Therapeutics Inc., Cambridge, Mass., is a biotechnology firm applying a new model for drug development to rare pediatric neuromuscular diseases. In the DART model, patient foundations join with biotechnology industry veterans to impact a central problem in rare diseases: Rapid therapy development. DART is focused on Duchenne muscular dystrophy, a fatal neuromuscular disease for which there is no effective treatment. For more information, please visit www.dartrx.com.

Media Contact: 
Shanti Skiffington 
617.921.0808 
shanti.skiffington(at)gmail.com

 


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