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Lux Biosciences Receives FDA Clearance for LX211 IND.
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PR Newswire
- Article date:
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November 28, 2006
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Copyright informationCOPYRIGHT 2006 PR Newswire Association LLC. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan. All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)
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-- Pipeline Milestone Paves The Way For Pivotal Trials Of Next Generation Calcineurin Inhibitor In Uveitis --
JERSEY CITY, N.J., Nov. 28 /PRNewswire/ -- Lux Biosciences, Inc., a privately held biotechnology company specialized in the field of ophthalmic diseases, announced today that the 30- day waiting period for its Investigational New Drug Application (IND) for the development of LX211 in uveitis has elapsed, paving the way for initiation of pivotal clinical trials in early 2007. The program consists of three controlled, double masked studies that will enroll a total of over 500 patients:
-- LX211-01 will investigate the use of LX211 as a steroid-sparing agent
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