Dehalogeno-compounds

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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Details

C514S303000, C514S305000, C514S299000, C546S119000, C546S121000, C546S123000, C546S153000, C546S156000

Reexamination Certificate

active

07902226

ABSTRACT:
3-(1-Aminocycloalkyl)pyrrolidinyl-substituted-6-dehalodeno(hydrogen-substituted)quinolon carboxylic acid derivatives having specific substituents as represented by the following formula (I), its salts, and hydrates thereof exhibit a broad and potent antibacterial activity on gram-negative and gram-positive bacteria, in particular, resistant bacteria typified by gram-positive cocci, including MRSA, PRSP and VRE. Thus these compounds are usable as drugs.

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Israeli Office Action dated Dec. 10, 2007.
Rejection on a JP application, pp. 1-11, mailed Nov. 4, 2004.
Koichi Yabe, et al., “Safety evaluation of antibacterial drugs (single intravenous dose toxicity study in mice)”, New Product Research Laboratories I, Daiichi Pharmaceutical Co., Ltd., Tokyo, Japan, prepared on Aug. 28, 2000 for internal distribution only.
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Katsuko Fujikawa, et al., “In Vitro Antibacterial Activity of DX-619, a Novel Des-Fluoro(6) Quinolone”, Antimicrobial Agents and Chemotherapy, Jul. 2005, p. 3040-3045, vol. 49, No. 7.
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Exhibit A: Data Summary, prepared on Mar. 2007 for purposes of accompanying IDS.
Exhibit B: Data Summary, prepared on Mar. 2007 for purposes of accompanying IDS.

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