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FVII or FVIIa Gla domain variants

a gla domain and variant technology, applied in the field of gla domain variants, can solve the problems of treatment being associated with a non-significant increase in thromboembolic events, and achieve the effect of reducing the number of thromboembolic events

Inactive Publication Date: 2005-07-28
BAYER HEALTHCARE LLC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0090] Consequently, it is contemplated that medical treatment with a polypeptide variant according to the invention may provide advantages over the currently available rhFVIIa compound (NovoSeven®), such as a lower dose, increased efficacy and / or faster action.

Problems solved by technology

However, it was also reported that the treatment was associated with a non-significant increase in thromboembolic events.

Method used

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  • FVII or FVIIa Gla domain variants
  • FVII or FVIIa Gla domain variants
  • FVII or FVIIa Gla domain variants

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0257] The X-ray structure of hFVIIa in complex with soluble tissue factor by Banner et al., J Mol Biol, 1996; 285:2089 is used for this example. For further information on the calculations in this example, see WO 01 / 58935.

Surface Exposure

[0258] Performing fractional ASA calculations resulted in the following residues being determined to have more than 25% of their side chain exposed to the surface: A1, N2, A3, F4, L5,E6,E7,L8,R9,P10,S12,L13,E14,E16,K18,E19,E20,Q21, S23,F24, E25, E26, R28, E29, F31, K32, D33, A34, E35, R36, K38, L39, W41, I42, S43, S45, G47, D48, Q49, A51, S52, S53, Q56, G58, S60, K62, D63, Q64, L65, Q66, S67, I69, F71, L73, P74, A75, E77, G78, R79, E82, T83, H84, K85, D86, D87, Q88, L89, I90, V92, N93, E94, G97, E99, S103, D104, H105, T106, G107, T108, K109, S111, R113, E116, G117, S119, L120, L121, A122, D123, G124, V125, S126, T128, P129, T130, V131, E132, I140, L141, E142, K143, R144, N145, A146, S147, K148, P149, Q150, G151, R152, G155, K157, V158, P160, K16...

example 2

Design of an Expression Cassette for Expression of rhFVII in Mammalian Cells

[0263] The expression cassette for expression of rhFVII was designed and cloned as described in Example 2 of WO 01 / 58935.

example 3

Construction of Expression Cassette Encoding Variants of the Invention

[0264] Sequence overhang extension (SOE) PCR was used for generating constructs having variant FVII open reading frames with substituted codons by using standard methods.

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PUM

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Abstract

Gla domain variants of human Factor VII or human Factor VIIa, comprising 1-15 amino acid modifications relative to human Factor VII or human Factor VIIa, wherein a hydrophobic amino acid residue has been introduced by substitution in position 34; or having an amino acid substitution in position 36; and use of the variants for the treatment of intracerebral haemorrhage (ICH) or trauma.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS [0001] This application is a continuation-in-part of International Patent Application No. PCT / DK2004 / 000428 filed on Jun. 18, 2004, which claims the benefit of U.S. Provisional Patent Application Ser. No. 60 / 479,780 filed on Jun. 19, 2003 and of Denmark Patent Application No. PA 2004 00930 filed on Jun. 15, 2004, the disclosures of each of which are incorporated by reference herein in their entirety for all purposes.FIELD OF THE INVENTION [0002] The present invention relates to novel Gla domain variants of Factor FVII (FVII) or Factor VIIa (FVIIa) polypeptides, as well as the use of such polypeptide variants in therapy, in particular for the treatment of a variety of coagulation-related disorders. BACKGROUND OF THE INVENTION [0003] Blood coagulation is a process consisting of a complex interaction of various blood components (or factors) that eventually results in a fibrin clot. Generally, the blood components participating in what has been re...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K38/00A61K38/37A61K38/48C12N9/64C12N15/57
CPCA61K38/4846C12Y304/21021C12N9/647C12N9/6437A61P17/02A61P7/04A61P9/10C07K14/745C12N15/52C12N9/64A61K38/36
Inventor HAANING, JESPERANDERSENBORNAES, CLAUS
Owner BAYER HEALTHCARE LLC
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