Medicament for the treatment of diseases caused by parasitic...

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Acyclic nitrogen double bonded to acyclic nitrogen – acyclic...

Reexamination Certificate

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C514S045000, C514S047000, C514S046000, C514S048000, C514S263400, C514S263370, C514S895000, C514S262100, C536S025320, C536S022100, C536S025310, C536S023100, C562S573000, C435S069100

Reexamination Certificate

active

10258810

ABSTRACT:
The present invention relates to the use of an inhibitor of CTP synthetase, such as a glutamine analogue, and a substance capable of suppressing toxic effects thereof in vivo, in the manufacture of a medicament for the treatment of a disease caused by a parasitic protozoa. More specifically, said substance capable of suppressing toxic effects may be a nucleobase, such as a purine base or a nucleoside, while the glutamine analogue advantageously is 6-diazo-5-oxo-L-norleucine (DON). The invention also relates to a pharmaceutical composition as such for the treatment and/or prevention of a disease caused by a parasitic protozoa, wherein the disease is selected from the group consisting of malaria, leishmaniasis and trypanosomiasis, e.g. American trypanosomiasis (Chaga's disease), or African trypanosomiasis (African sleeping sickness).

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patent: 5776718 (1998-07-01), Palmer et al.
patent: 6159953 (2000-12-01), Rathod
patent: 6242428 (2001-06-01), Weis et al.
patent: 98/31375 (1998-07-01), None
Queen et al. “In vitro susceptibilities of Plasmodium falciparum to compounds which inhibit nucleotide metabolism.” Antimicrob Agents and Chemotherapy, Jul. 1990, 34(7), pp. 1393-1398.
Mukherjee et al. “Acivicn: A highly active potential chemotherapeutic agent against visceral leishmaniasis.” Biochemical and Biophysical Research Communications, vol. 170, No. 2, pp. 426-432, 1990.
Tanmoy Mukherjee et al, “Acivicin: A Highly Active Potential Chemotherapeutic Agent Against Visceral Leishmaniasis,” Biochemical and Biophysical Research Communications, vol. 170, No. 2, pp. 426-432, 1990.
Takashi Aoki et al, “Quantitative Determination of Trypanosoma Cruzi Growth inside Host Cells In Vitro and Effect of Allopurinol,” Purine and Pyrimidine Metabolism in Man VIII, pp. 499-502, 1994.
Kenneth E. Kinnamon et al, “Activity of Anticancer Compounds Against Trypanosoma Cruzi-Infected Mice,” Am. J. Trop. Med. Hyg., vol. 58, No. 6, pp. 804-806, 1998.
Kim E. Nichols et al, “Monocytoid Differentiation of Freshly Isolated Human Myeloid Leukemia Cells and HL-60 Cells Induced by the Glutamine Antagonist Acivicin,” Blood, vol. 74, No. 5, pp. 1728-1737, 1989.

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