Logical Therapeutics has completed its Phase Ib randomized controlled multi-dose safety and pharmacokinetics study of LT-NS001, the company's proprietary naproxen prodrug.
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The study, which was conducted in normal adult volunteers, showed that LT-NS001 was well-tolerated by the recipients. Moreover, when the subjects in the study were dosed twice daily with LT-NS001 for seven days, plasma concentrations of naproxen were within the therapeutic range.
LT-NS001 is a prodrug, which is converted in the bloodstream into naproxen, a non-steroidal anti-inflammatory drug. The company expects to begin enrolling subjects in its next clinical study of LT-NS001 later 2008.
Mitchell Fink, president and CEO of Logical Therapeutics, said: “The results from our recently completed Phase Ib study of LT-NS001 are very encouraging, because they show that administration of the pro-drug leads to clinically useful circulating levels of naproxen.”
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