Abstract: Disclosed is a method of preparing a solution adapted for administration by infusion, comprising a) a compound having the formula (I): and/or a compound having the formula (II): and b) two different sodium phosphate salts, wherein the two different sodium phosphate salts are NaH2PO4·2H2O and Na2HPO4·2H2O, and wherein the quantity of the NaH2PO4·2H2O and Na2HPO4·2H2O present in the composition is chosen such that the molar ratio of both NaH2PO4·H2O and Na2HPO4·2H2O to compound (I) or compound (II) ranges from 0.02 to 0.5 and optionally NaCl. Also disclosed is a method of treating a disease in a subject, comprising the step of administering to a subject in need thereof a reconstituted solution as disclosed.
Type:
Application
Filed:
July 20, 2023
Publication date:
November 9, 2023
Applicant:
VASOPHARM GMBH
Inventors:
Peter SCHEURER, Frank TEGTMEIER, Reinhard SCHINZEL
Abstract: The present invention relates to a method for preparing a lyophilized solid pharmaceutical composition comprising a) a compound having the formula (I): and/or a compound having the formula (II): ?and b) two different sodium phosphate salts, wherein the two different sodium phosphate salts are NaH2PO4·2H2O and Na2HPO4·2H2O, and wherein the quantity of the NaH2PO4·2H2O and Na2HPO4·2H2O present in the composition is chosen such that the molar ratio of both NaH2PO4·2H2O and Na2HPO4·2H2O to compound (I) or compound (II) ranges from 0.02 to 0.5.
Type:
Grant
Filed:
January 20, 2021
Date of Patent:
August 8, 2023
Assignee:
VASOPHARM GMBH
Inventors:
Peter Scheurer, Frank Tegtmeier, Reinhard Schinzel
Abstract: The present invention relates to a method for preparing a lyophilized solid pharmaceutical composition comprising a) a compound having the formula (I): and/or a compound having the formula (II): and b) two different sodium phosphate salts, wherein the two different sodium phosphate salts are NaH2PO4.2H2O and Na2HPO4.2H2O, and wherein the quantity of the NaH2PO4.2H2O and Na2HPO4.2H2O present in the composition is chosen such that the molar ratio of both NaH2PO4.2H2O and Na2HPO4.2H2O to compound (I) or compound (II) ranges from 0.02 to 0.5.
Type:
Application
Filed:
January 20, 2021
Publication date:
February 3, 2022
Applicant:
VASOPHARM GMBH
Inventors:
Peter SCHEURER, Frank TEGTMEIER, Reinhard SCHINZEL
Abstract: The present invention relates to a method for preparing a lyophilized solid pharmaceutical composition comprising a) a compound having the formula (I): and/or a compound having the formula (II): and b) two different sodium phosphate salts, wherein the two different sodium phosphate salts are NaH2PO4.2H2O and Na2HPO4.2H2O, and wherein the quantity of the NaH2PO4.2H2O and Na2HPO4.2H2O present in the composition is chosen such that the molar ratio of both NaH2PO4.2H2O and Na2HPO4.2H2O to compound (I) or compound (II) ranges from 0.02 to 0.5.
Type:
Application
Filed:
January 20, 2021
Publication date:
May 13, 2021
Applicant:
VASOPHARM GMBH
Inventors:
Peter SCHEURER, Frank TEGTMEIER, Reinhard SCHINZEL
Abstract: Compositions comprising derivatives of biopterin, useful for the treatment of traumatic brain injury, non-traumatic brain injury, elevated cranial pressure, and secondary brain injury.
Type:
Grant
Filed:
October 21, 2019
Date of Patent:
February 23, 2021
Assignee:
VASOPHARM GMBH
Inventors:
Peter Scheurer, Frank Tegtmeier, Reinhard Schinzel
Abstract: The present invention relates to a method of treating a disease in a subject, comprising administering to a subject in need thereof a solid pharmaceutical composition biopterin derivatives.
Type:
Grant
Filed:
May 2, 2017
Date of Patent:
July 10, 2018
Assignee:
VASOPHARM GMBH
Inventors:
Peter Scheurer, Frank Tegtmeier, Reinhard Schinzel
Abstract: The present invention relates to solid pharmaceutical compositions comprising biopterin derivatives as well as methods for obtaining such solid pharmaceutical compositions. The invention also relates to the solid pharmaceutical compositions of the invention for treating diseases.
Type:
Grant
Filed:
March 30, 2015
Date of Patent:
February 20, 2018
Assignee:
VASOPHARM GMBH
Inventors:
Peter Scheurer, Frank Tegtmeier, Reinhard Schinzel
Abstract: The present invention relates to the use of pteridine derivatives for the treatment of increased intracranial pressure, secondary ischemia, and disorders associated with an increased level of cytotoxic reactive oxygen species.
Abstract: The present invention relates to the use of pteridine derivatives for the treatment of increased intracranial pressure, secondary ischemia, and disorders associated with an increased level of cytotoxic reactive oxygen species.
Abstract: The present invention relates to the use of pteridine derivatives for the treatment of increased intracranial pressure, secondary ischemia, and disorders associated with an increased level of cytotoxic reactive oxygen species.
Abstract: The invention relates to compounds of formula het-X-AB containing a N-heteroaryl moiety “het”, which is linked via X=sulfur to the 1,2,3-triazolo[4,5-d]pyrimidine-7-yl moiety AB of the formula (II). The invention also relates to a process for the preparation of said compounds and the use thereof in drugs for the treatment of NAD(P)H oxidase-related diseases and disorders and inhibition of platelet activation.
Type:
Grant
Filed:
May 13, 2005
Date of Patent:
August 7, 2012
Assignee:
Vasopharm GmbH
Inventors:
Frank Tegtmeier, Ulrich Walter, Reinhard Schinzel, Kirstin Wingler, Peter Scheurer, Harald Schmidt
Abstract: The present invention relates to the area of NO synthase inhibition and, more particularly, relates to novel 4-amino-7,8-dihydropteridines, pharmaceutical compositions containing said compounds, and the use of said compounds in the treatment of a disorder characterized by a disturbed nitric oxide level.