Patents by Inventor Robert D. Gordon
Robert D. Gordon has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).
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Publication number: 20220193046Abstract: An extended release oral dosage form comprising as active substance tacrolimus or a pharmaceutically active analogue thereof for a once daily immunosuppressive treatment of a patient in need thereof, preferable a kidney or liver transplant patient. The dosage form releases the active substance over an extended period of time. It also provides improved pharmacokinetic parameters due to an extended and constant in vivo release including substantial decreased peak concentrations, despite increased bioavailability, substantial extended times for maximal concentration, and higher minimal concentrations when compared with conventional immediate release dosage forms and a recent modified release tacrolimus dosage form.Type: ApplicationFiled: August 4, 2021Publication date: June 23, 2022Inventors: Robert D Gordon, Per Holm, Anne-Marie Lademann, Tomas Norling
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Patent number: 11123331Abstract: An extended release oral dosage form comprising as active substance tacrolimus or a pharmaceutically active analogue thereof for a once daily immunosuppressive treatment of a patient in need thereof, preferable a kidney or liver transplant patient. The dosage form releases the active substance over an extended period of time. It also provides improved pharmacokinetic parameters due to an extended and constant in vivo release including substantial decreased peak concentrations, despite increased bioavailability, substantial extended times for maximal concentration, and higher minimal concentrations when compared with conventional immediate release dosage forms and a recent modified release tacrolimus dosage form.Type: GrantFiled: October 30, 2020Date of Patent: September 21, 2021Assignee: VELOXIS PHARMACEUTICALS, INC.Inventors: Robert D. Gordon, Per Holm, Anne-Marie Lademann, Tomas Norling
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Patent number: 11110081Abstract: An extended release oral dosage form comprising as active substance tacrolimus or a pharmaceutically active analogue thereof for a once daily immunosuppressive treatment of a patient in need thereof, preferable a kidney or liver transplant patient. The dosage form releases the active substance over an extended period of time. It also provides improved pharmacokinetic parameters due to an extended and constant in vivo release including substantial decreased peak concentrations, despite increased bioavailability, substantial extended times for maximal concentration, and higher minimal concentrations when compared with conventional immediate release dosage forms and a recent modified release tacrolimus dosage form.Type: GrantFiled: October 30, 2020Date of Patent: September 7, 2021Assignee: VELOXIS PHARMACEUTICALS, INC.Inventors: Robert D. Gordon, Per Holm, Anne-Marie Lademann, Tomas Norling
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Publication number: 20210046055Abstract: An extended release oral dosage form comprising as active substance tacrolimus or a pharmaceutically active analogue thereof for a once daily immunosuppressive treatment of a patient in need thereof, preferable a kidney or liver transplant patient. The dosage form releases the active substance over an extended period of time. It also provides improved pharmacokinetic parameters due to an extended and constant in vivo release including substantial decreased peak concentrations, despite increased bioavailability, substantial extended times for maximal concentration, and higher minimal concentrations when compared with conventional immediate release dosage forms and a recent modified release tacrolimus dosage form.Type: ApplicationFiled: October 30, 2020Publication date: February 18, 2021Inventors: Robert D. GORDON, Per HOLM, Anne-Marie LADEMANN, Tomas NORLING
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Publication number: 20210046054Abstract: An extended release oral dosage form comprising as active substance tacrolimus or a pharmaceutically active analogue thereof for a once daily immunosuppressive treatment of a patient in need thereof, preferable a kidney or liver transplant patient. The dosage form releases the active substance over an extended period of time. It also provides improved pharmacokinetic parameters due to an extended and constant in vivo release including substantial decreased peak concentrations, despite increased bioavailability, substantial extended times for maximal concentration, and higher minimal concentrations when compared with conventional immediate release dosage forms and a recent modified release tacrolimus dosage form.Type: ApplicationFiled: October 30, 2020Publication date: February 18, 2021Inventors: Robert D. GORDON, Per HOLM, Anne-Marie LADEMANN, Tomas NORLING
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Patent number: 10864199Abstract: An extended release oral dosage form comprising as active substance tacrolimus or a pharmaceutically active analogue thereof for a once daily immunosuppressive treatment of a patient in need thereof, preferable a kidney or liver transplant patient. The dosage form releases the active substance over an extended period of time. It also provides improved pharmacokinetic parameters due to an extended and constant in vivo release including substantial decreased peak concentrations, despite increased bioavailability, substantial extended times for maximal concentration, and higher minimal concentrations when compared with conventional immediate release dosage forms and a recent modified release tacrolimus dosage form.Type: GrantFiled: February 11, 2016Date of Patent: December 15, 2020Assignee: VELOXIS PHARMACEUTICALS A/SInventors: Robert D. Gordon, Per Holm, Anne-Marie Lademann, Tomas Norling
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Publication number: 20160243091Abstract: An extended release oral dosage form comprising as active substance tacrolimus or a pharmaceutically active analogue thereof for a once daily immunosuppressive treatment of a patient in need thereof, preferable a kidney or liver transplant patient. The dosage form releases the active substance over an extended period of time. It also provides improved pharmacokinetic parameters due to an extended and constant in vivo release including substantial decreased peak concentrations, despite increased bioavailability, substantial extended times for maximal concentration, and higher minimal concentrations when compared with conventional immediate release dosage forms and a recent modified release tacrolimus dosage form.Type: ApplicationFiled: February 11, 2016Publication date: August 25, 2016Inventors: Robert D. GORDON, Per HOLM, Anne-Marie LADEMANN, Tomas NORLING
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Publication number: 20140179731Abstract: An extended release oral dosage form comprising as active substance tacrolimus or a pharmaceutically active analogue thereof for a once daily immunosuppressive treatment of a patient in need thereof, preferable a kidney or liver transplant patient. The dosage form releases the active substance over an extended period of time. It also provides improved pharmacokinetic parameters due to an extended and constant in vivo release including substantial decreased peak concentrations, despite increased bioavailability, substantial extended times for maximal concentration, and higher minimal concentrations when compared with conventional immediate release dosage forms and a recent modified release tacrolimus dosage form.Type: ApplicationFiled: December 26, 2013Publication date: June 26, 2014Applicant: Veloxis Pharmaceuticals A/SInventors: Robert D. Gordon, Per Holm, Anne-Marie Lademann, Tomas Norling
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Patent number: 8685998Abstract: An extended release oral dosage form comprising as active substance tacrolimus or a pharmaceutically active analogue thereof for a once daily immunosuppressive treatment of a patient in need thereof, preferable a kidney or liver transplant patient. The dosage form releases the active substance over an extended period of time. It also provides improved pharmacokinetic parameters due to an extended and constant in vivo release including substantial decreased peak concentrations, despite increased bioavailability, substantial extended times for maximal concentration, and higher minimal concentrations when compared with conventional immediate release dosage forms and a recent modified release tacrolimus dosage form.Type: GrantFiled: July 7, 2009Date of Patent: April 1, 2014Assignee: Veloxis Pharmaceuticals A/SInventors: Robert D. Gordon, Per Holm, Anne-Marie Lademann, Tomas Norling
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Patent number: 8664239Abstract: An extended release oral dosage form comprising as active substance tacrolimus or a pharmaceutically active analogue thereof for a once daily immunosuppressive treatment of a patient in need thereof, preferable a kidney or liver transplant patient. The dosage form releases the active substance over an extended period of time. It also provides improved pharmacokinetic parameters due to an extended and constant in vivo release including substantial decreased peak concentrations, despite increased bioavailability, substantial extended times for maximal concentration, and higher minimal concentrations when compared with conventional immediate release dosage forms and a recent modified release tacrolimus dosage form.Type: GrantFiled: June 23, 2011Date of Patent: March 4, 2014Assignee: Veloxis Pharmaceuticals A/SInventors: Robert D. Gordon, Per Holm, Anne-Marie Lademann, Tomas Norling
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Patent number: 8135603Abstract: The method of applying constraints across a generally extensible and configurable resource delivery system as a basis for identifying or calculating the relative impacts of each constraint on resource delivery to various points and, through the use of constraint release mechanisms, developing prescriptive courses of action to optimize and increase the certainty of delivery of the resource, or in the reverse sense, restrict delivery of the resource. In an embodiment of the present invention, a method for characterizing the availability and potential use of water resources alongside associated impacts in order to identify and time the various policy decisions and investments needed to ensure access to water supplies over time given multiple stakeholders and uncertain, variable supplies and demands where such embodiment provides additional methods generally applicable across the full scope of embodiments of the invention.Type: GrantFiled: March 20, 2008Date of Patent: March 13, 2012Inventor: Robert D. Gordon
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Publication number: 20120029009Abstract: An extended release oral dosage form comprising as active substance tacrolimus or a pharmaceutically active analogue thereof for a once daily immunosuppressive treatment of a patient in need thereof, preferable a kidney or liver transplant patient. The dosage form releases the active substance over an extended period of time. It also provides improved pharmacokinetic parameters due to an extended and constant in vivo release including substantial decreased peak concentrations, despite increased bioavailability, substantial extended times for maximal concentration, and higher minimal concentrations when compared with conventional immediate release dosage forms and a recent modified release tacrolimus dosage form.Type: ApplicationFiled: June 23, 2011Publication date: February 2, 2012Applicant: LifeCycle Pharma A/SInventors: Robert D. Gordon, Per Holm, Anne-Marie Lademann, Tomas Norling
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Publication number: 20110275659Abstract: An extended release oral dosage form comprising as active substance tacrolimus or a pharmaceutically active analogue thereof for a once daily immunosuppressive treatment of a patient in need thereof, preferable a kidney or liver transplant patient. The dosage form releases the active substance over an extended period of time. It also provides improved pharmacokinetic parameters due to an extended and constant in vivo release including substantial decreased peak concentrations, despite increased bioavailability, substantial extended times for maximal concentration, and higher minimal concentrations when compared with conventional immediate release dosage forms and a recent modified release tacrolimus dosage form.Type: ApplicationFiled: June 23, 2011Publication date: November 10, 2011Applicant: LifeCycle Pharma A/SInventors: Robert D. GORDON, Per HOLM, Anne-Marie LADEMANN, Tomas NORLING
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Publication number: 20100105717Abstract: An extended release oral dosage form comprising as active substance tacrolimus or a pharmaceutically active analogue thereof for a once daily immunosuppressive treatment of a patient in need thereof, preferable a kidney or liver transplant patient. The dosage form releases the active substance over an extended period of time. It also provides improved pharmacokinetic parameters due to an extended and constant in vivo release including substantial decreased peak concentrations, despite increased bioavailability, substantial extended times for maximal concentration, and higher minimal concentrations when compared with conventional immediate release dosage forms and a recent modified release tacrolimus dosage form.Type: ApplicationFiled: July 7, 2009Publication date: April 29, 2010Applicant: LifeCycle Pharma A/SInventors: Robert D. Gordon, Per Holm, Anne-Marie Lademann, Tomas Norling
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Patent number: 7179890Abstract: There is provided a novel vascular endothelial growth factor, herein designated VEGF-X, in addition to the nucleic acid molecule encoding it, a host cell transformed with said vector and compounds which inhibit or enhance angiogenesis. Also provided is the sequence of a CUB domain present in the sequence of VEGF-X which domain itself prevents angiogenesis and which is used to treat diseases associated with inappropriate vascularisation or angiogenesis.Type: GrantFiled: August 23, 2004Date of Patent: February 20, 2007Assignee: Janssen Pharmaceutica.N.V.Inventors: Robert D. Gordon, Jörg J. Sprengel, Jeffrey R. Yon, Josiena J. H. Dijkmans, Anna Gosiewska, Sridevi N. Dhanaraj, Jean Xu
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Patent number: 6783953Abstract: There is provided a novel vascular endothelial growth factor, herein designated VEGF-X, in addition to the nucleic acid molecule encoding it, a host cell transformed with said vector and compounds which inhibit or enhance angiogenesis. Also provided is the sequence of a CUB domain present in the sequence of VEGF-X which domain itself prevents angiogenesis and which is used to treat diseases associated with inappropriate vascularisation or angiogenesis.Type: GrantFiled: December 21, 1999Date of Patent: August 31, 2004Assignee: Janssen Pharmaceutica N.V.Inventors: Robert D. Gordon, Jörg J. Sprengel, Jeffrey R. Yon, Josiena J. H. Dijkmans, Anna Gosiewska, Sridevi N. Dhanaraj, Jean Xu
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Publication number: 20040115213Abstract: The invention relates to a method for treating a patient having a fungal infection. The invention comprises administering to the patient a therapeutically effective amount of a polyene antifungal (e.g., amphotericin B) in association with a therapeutically effective amount of a interleukin-2 inhibitor (e.g., chimeric or humanized monoclonal antibody that binds to the p55 subunit of the human interleukin-2 receptor and inhibits binding of interleukin-2 to an interleukin-2 receptor).Type: ApplicationFiled: October 1, 2003Publication date: June 17, 2004Inventors: Stanley Willetts Chapman, John Dale Cleary, Robert D. Gordon
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Patent number: 5491778Abstract: A system is provided for generating transition effects for use on a visual display. The system includes a binary table for describing a transition effect and a method for ordering the rows in the table to produce the transition. The table includes an arbitrary number of rows, each row representing a cell (group of picture elements) on the display. A numerical value, based on any function of cell location, is associated with each cell. The table is then sorted according to the numerical values. Each row in the sorted table drives a step in the transition effect. The cells described by the various rows are changed in sorted order to display the material from the image being transitioned-to. The sequence of processing of the rows causes the desired transition effect. By varying the function used to order the rows, an infinite variety of transition effects can be created.Type: GrantFiled: October 17, 1994Date of Patent: February 13, 1996Assignee: International Business Machines CorporationInventors: Robert D. Gordon, Joseph F. Sinnott, Jr., Lonnie S. Walling
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Patent number: 5414805Abstract: A computer system generates transition effects for use on a visual display. The system includes a binary table for describing a transition effect and a method for ordering the rows in the table to produce the transition. The table includes an arbitrary number of rows, each row representing a cell (group of picture elements) on the display. A numerical value, based on any function of cell location, is associated with each cell. The table is then sorted according to the numerical values. Each row in the sorted table drives a step in the transition effect. The cells described by the various rows are changed in sorted order to display the material from the image being transitioned-to. The sequence of processing of the rows causes the desired transition effect. By varying the function used to order the rows, an infinite variety of transition effects can be created.Type: GrantFiled: November 6, 1992Date of Patent: May 9, 1995Assignee: International Business Machines CorporationInventors: Robert D. Gordon, Joseph F. Sinnott, Jr., Lonnie S. Walling
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Patent number: 5390289Abstract: A method of generating a second, substantially anti-aliased, representation of a character from a first representation. The second representation is comprised of horizontal lines of dots that are shifted horizontally relative to dots of the first representation, each dot of the first representation having a value DOT1 associated therewith. The method include a step of, for each horizontal line (1-m) within the first representation of a character and for each dot (1-j) within a horizontal line, (a) determining a modifying value (DOT1k) associated with a dot(k) of the first representation, DOT1k being a function of DOT1 of the dot(k). The method includes another step of determining a value (DOT2k) of a corresponding dot for the second representation, the value of the corresponding dot being determined in accordance with the expression DOT2k=((DOT1-DOT1k )+DOT1(k-1)), where DOT1(k-1) is a modifying value of an adjacent dot on the horizontal line.Type: GrantFiled: December 17, 1993Date of Patent: February 14, 1995Assignee: International Business Machines CorporationInventors: Bradley J. Beitel, Robert D. Gordon, Joseph B. Witherspoon, III