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ML 3000

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Table I
Table II

Notes

  1. This profile has been selected from R&D Insight™, a pharmaceutical intelligence database produced by Adis International Ltd.

References

  1. Wallace JL, Carter L, McKnight W, Tries S, Laufer S. ML 3000 reduces gastric prostaglandin synthesis without causing mucosal injury. Eur J Pharmacol 271: 525–531, 27 Dec 1994

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  3. Euro Alliance. First clinical results of ML 3000, the parent drug of a new category of antiinflammatory agents, the Double Acting Antiinflammatory Drugs (DAAID). Company Communication: [2 pages], 11 Feb 1998

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  4. Forest Laboratories Inc. Forest Laboratories announces positive results with ML3000 in early clinical trials. Media Release: [2 pages], 6 Oct 2000. Available from URL: http://www.frx.com

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  5. Laufer S, Tries S, Augustin J, Dannhardt G. Pharmacological profile of a new pyrrolizine derivative inhibiting the enzymes cyclo-oxygenase and 5-lipoxygenase. Arzneimittel-Forschung 44: 629–636, Part 1, May 1994

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  6. Laufer S, Tries S, Augustin J, et al. Acute and chronic antiinflammatory properties of [2,2-dimethyl-6-(4-chlorophenyl) -7-phenyl-2,3-dihydro-1H-pyrrolizine-5-yl-]-acetic acid. Arzneimittel-Forschung 45: 27–32, Jan 1995

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ML 3000. Drugs R&D 3, 204–207 (2002). https://doi.org/10.2165/00126839-200203030-00014

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