Crystalline chemotherapeutic

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

C514S409000, C548S362100

Reexamination Certificate

active

07994208

ABSTRACT:
N-[4-(3-Amino-1H-indazol-4-yl)phenyl]-N′-(2-fluoro-5-methylphenyl)urea·¼ Ethanolate Crystalline Form 1, ways to make it, formulations comprising it and made with it and methods of treating patients having disease using it is disclosed.

REFERENCES:
patent: 7297709 (2007-11-01), Dai et al.
patent: 2005/0020603 (2005-01-01), Dai et al.
patent: WO2004113304 (2004-12-01), None
patent: WO2007050574 (2007-05-01), None
U.S. Pharmacopoeia, pp. 1843-1884 (1995).
Dai, et al, “Discover of N-(4-(3-Amino-1H-indazol-4-yl)phenyl)-N′-(2-fluoro-5-methylphenyl)urea (ABT-869), a 3-Aminoindazole-Based Orally Active Multitargeted Receptor Tyrosine Kinase Inhibitor”, J. Med. Chem., 50, 1584-1597 (2007).
International Search Report PCT, Jan. 19, 2009.
Aulton M.E., ed., Pharmaceutics: The Science of Dosage Form Design, 2nd Edition, Churchill Livingstone, 2004, Table of Contents.
Hilfiker R., ed., Polymorphism in the Pharmaceutical Industry, Wiley-VCH Verlag GmbH & Co., KGaA, Weinheim, Germany, 2006, Table of Contents.
Morris K.M., “Structural Aspects of Hydrate and Solvates,” Polymorphism in Pharmaceutical Solids, 1999, pp. 125-181.

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