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Cystic Fibrosis

Drug delivery company signs licensing agreement for Cystic Fibrosis treatment

Published in Gene Therapy Weekly, October 28th, 2004

Oriel Therapeutics announced that it has signed a development and licensing agreement with an undisclosed U.S.-based biotechnology company to develop a novel therapy for the treatment of cystic fibrosis.

This therapy will be based on Oriel Therapeutics' proprietary dry powder inhalation technology incorporating the partner's proprietary compounds that represent a novel mode of action to improve airway function.

Cystic fibrosis is a genetic disorder that affects approximately 30,000 children and adults in the United States. The disease causes the body to produce abnormally thick, sticky mucus that clogs the lungs and leads to life-threatening...

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