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filingDate 2012-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 2017-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2646191-T3
titleOfInvention Factor XII inhibitors for administration with medical procedures comprising contact with artificial surfaces
abstract FXII / FXIIa inhibitor for use in the prevention of thrombus formation and / or stabilization during and / or after a medical procedure carried out on a human or animal subject comprising contacting blood of said human or animal subject with artificial surfaces, where said FXII / FXIIa inhibitor is administered before and / or during and / or after said medical procedure and also where (i) the artificial surface is exposed to at least 80% of the subject's blood volume and the artificial surface is at least 0.2 m2 or (ii) the artificial surface is a vessel for blood collection outside the subject's body or (iii) the artificial surface is a stent, valve, intraluminal catheter or a pumping system of internal assisted blood, where the FXII / FXIIa inhibitor comprises (i) the naturally occurring Infestin-4 polypeptide sequence (SEQ ID NO: 1) or a variant thereof, where a variant comprises (a) the amino acids N-terminal 2-13 of the naturally occurring Infestin-4 sequence and at least one and up to five amino acid mutations outside said N-terminal amino acids that give rise to differences with respect to the naturally occurring Infestin-4 sequence; and / or (b) six conserved cysteine residues of the naturally occurring Infestin-4 sequence and a homology of at least 70% with respect to the naturally occurring Infestin-4 sequence. (ii) SPINK-1 (SEQ ID NO: 2), which is mutated to include N-terminal amino acids 2-13 of the naturally occurring Infestin-4 sequence, or a variant of said mutated SPINK-1, where a variant comprises (a) the N-terminal amino acids 2-13 of the naturally occurring Infestin-4 sequence and at least one and up to five amino acid mutations outside of said N-terminal amino acids that give rise to differences with respect to the sequence of SPINK-1 of natural origin and that increase the homology of the variant with respect to the sequence of Infestina-4 of natural origin; and / or (b) six cysteine residues conserved from the naturally occurring SPINK-1 sequence and at least 70% homology to the naturally occurring SPINK-1 sequence. (iii) an anti-FXII / FXIIa antibody, where the antibody binds to FXII / FXIIa and inhibits its activity and / or activation.
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Total number of triples: 439.