AVI Biopharma, the Portland, OR-based developer of RNA-based therapies, said today it has secured $1.2 million in funding over the next year from Action Duchenne, a U.K.-based charity that supports research into Duchenne Muscular Dystrophy. The agreement has an option to be extended for additional years, AVI said. The company (NASDAQ: [[ticker:AVII]]) is developing a drug called AVI-4658, which is supposed to allow patients to produce a functional copy of a protein called dystrophin. The company has tested an injectable version of this drug in boys with the disease, and is now working on a version that can be delivered throughout the body.
Author: Luke Timmerman
Luke is an award-winning journalist specializing in life sciences. He has served as national biotechnology editor for Xconomy and national biotechnology reporter for Bloomberg News. Luke got started covering life sciences at The Seattle Times, where he was the lead reporter on an investigation of doctors who leaked confidential information about clinical trials to investors. The story won the Scripps Howard National Journalism Award and several other national prizes. Luke holds a bachelor’s degree in journalism from the University of Wisconsin-Madison, and during the 2005-2006 academic year, he was a Knight Science Journalism Fellow at MIT.
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