Method for treating gastric disorders using optically pure...

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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Reexamination Certificate

active

06953808

ABSTRACT:
Methods and compositions are disclosed utilizing optically pure (−) pantoprazole for the treatment of ulcers in humans while substantially reducing the concomitant liability of adverse effects associated with the racemic mixture of pantoprazole. The optically pure (−) isomer is also useful for the treatment of gastroesophageal reflux. (−) Pantoprazole is an inhibitor of H+release and is therefore useful in the treatment of other conditions related to gastric hypersecretion such as Zollinger-Ellison Syndrome.

REFERENCES:
patent: 4758579 (1988-07-01), Kohl et al.
patent: 5888535 (1999-03-01), Gray
patent: 4035455 (1992-05-01), None
Kohl et al. “(H+,K+)-ATPase Inhibiting 2-[(2-Pyridylmethyl) sulfinyl] benzimidazoles . . . ”J. Med. Chem.35, 1049-1057 (1992).
Kromer et al. “BY 1023/SK&F 96033 INN pantoprazole, a Novel Gastric Proton Pump Inhibitor, Potently Inhibits Acid Secretion But Lacks Relevant . . . ”J. Pharm. Exp. Ther.254, 129-135 (1990).
Simon et al. “Single Intravenous Administration of the H+K+-ATPase inhibitor BU 1023/SK&F 96022-inhibition of pentagastrin-stimulated gastric acid . . . ”Aliment. Pharmacol. Therap.4, 239-245 (1990).
Beil et al. “Pantoprazole: a novel H+/K+-ATPase inhibitor with an improved pH stability”Eur. J. Pharm.218 265-271 (1992).
Kromer et al. “Direct Comparison between the Ulcer-Healing Effects of Two H+-K+-ATPase Inhibitors, One M1-Selective Antimuscarinic and One H2Receptor Antagonist in the Rat”Pharmacology41 333-337 (1990).
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Decktor et al. “Acute Effects of Ranitidine, Famotidine and Omeprazole on Plasma Gastrin in the Rat”J. Pharm. Exp. Ther.249, 1-5 (1989).
Hannan et al. “Effects of oral pantoprazole on 24-hour intragastric acidity and plasma gastrin profiles”Aliment. Pharmacol. Ther.6 373-380 (1992).
Simon et al. “Effect of repeated oral administration of BY1023/SK&F96022—a new substituted benzimidazole derivative—on pentagastrin-stimulated gastric acid secretion . . . ”Aliment. Pharmacol. Therap.4, 373-379 (1990).
Simon et al. “BY 1023/SK&F 96022: Biochemistry of a Novel (H++K+) ATPase Inhibitor”Biochem. Pharm.39 1799-1806 (1990).
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Simon et al. “Pentagastrin-stimulated gastric acid secretion and pharmacokinetics following . . . ”Z. Gastroenterol28 443-447 (1990).

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