Abstract: The invention relates to a compound suitable for inhibiting the influx of polymorphonuclear leukocytes (PMNs) into a tissue involved in a chronic inflammatory disease. The compound according to the invention is capable of forming a complex with N-acetyl-Pro-Gly-Pro. The invention also relates to a method of selecting such a compound, a pharmaceutical composition and an application of the compound.
Type:
Grant
Filed:
August 22, 2005
Date of Patent:
August 12, 2008
Assignee:
Fornix Biosciences N.V.
Inventors:
Franciscus Petrus Nijkamp, Rosswell Robert Pfister, Jeffrey Lynn Haddox, James Edwin Blalock, Matteo Villain
Abstract: The invention provides a vector which is capable of the expression of a vascular endothelial growth factor wherein the vector comprises a modified PCMV promoter. The invention further provides use of a vector which is capable of and expressing a vascular endothelial growth factor (VEGF) for the regulation of endothelial function, angiogenesis and arteriogenesis. The invention further comprises use of a vector which is capable of the expression of a vascular endothelial growth factor (VEGF) for the prophylactic treatment of arterial diseases and/or bone marrow diseases and/or neural diseases.
Type:
Grant
Filed:
May 23, 2002
Date of Patent:
May 29, 2007
Assignee:
Fornix Biosciences N.V.
Inventors:
Tjerk Johannes A. Visser, Folkert Feiko Roossien, Carola Jacoba M. Ubink-Bontekoe
Abstract: The invention relates to a compound inhibiting the binding of the free light chain of immunoglobulin (Ig LC) to mast cells. It has been found that Ig LC is the agent responsible for the sensitization of mast cells. The compounds according to the invention can thus be used for the preparation of a drug for the treatment of a disease whose symptom is an elevated Ig LC concentration in serum or spinal fluid. The invention also relates to a method of screening a series of compounds on their ability to reduce the sensitization of mast cells.
Abstract: The invention relates to a compound suitable for inhibiting the influx of polymorphonuclear leukocytes (PMNs) into a tissue involved in a chronic inflammatory disease. The compound according to the invention is capable of forming a complex with N-acetyl-Pro-Gly-Pro. The invention also relates to a method of selecting such a compound, a pharmaceutical composition and an application of the compound.
Type:
Grant
Filed:
November 13, 2003
Date of Patent:
November 1, 2005
Assignee:
Fornix Biosciences N.V.
Inventors:
Franciscus Petrus Nijkamp, Rosswell Robert Pfister, Jeffrey Lynn Haddox, James Edwin Blalock, Matteo Villain
Abstract: The present invention is directed to a series of complementary peptides for the pro-gly-pro sequence as antagonists of polymorphonuclear leukocyte chemoattractants. Also provided are applications of such peptides for treating alkali-injuried eyes and other types of diseases.
Type:
Grant
Filed:
September 28, 2001
Date of Patent:
July 13, 2004
Assignee:
Fornix Biosciences N.V.
Inventors:
Jeffrey Lynn Haddox, Roswell Robert Pfister, James Edwin Blalock, Matteo Villain
Abstract: The present invention is directed to a series of complementary peptides for the pro-gly-pro sequence as antagonists of polymorphonuclear leukocyte chemoattractants. Also provided are applications of such peptides for treating alkali-injuried eyes and other types of diseases.
Type:
Grant
Filed:
March 8, 2000
Date of Patent:
October 30, 2001
Assignee:
Fornix Biosciences N.V.
Inventors:
Jeffrey Lynn Haddox, Roswell Robert Pfister, James Edwin Blalock, Matteo Villain