Patents Represented by Attorney, Agent or Law Firm Mark J. Stewart
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Patent number: 7320790Abstract: Humanized forms of mouse antibody 10D5 that retain the binding properties of mouse 10D5 are disclosed. Also disclosed are processes for making the humanized antibody, intermediates for making the humanized antibodies, including, nucleotide sequences, vectors, transformed host cells, and methods of using the humanized antibody to treat, prevent, alleviate, reverse, or otherwise ameliorate symptoms or pathology or both, that are associated with Down's syndrome or pre-clinical or clinical Alzheimer's disease or cerebral amyloid angiopathy.Type: GrantFiled: April 26, 2002Date of Patent: January 22, 2008Assignee: Eli Lilly and CompanyInventors: Paul Robert Hinton, Maximiliano J. Vasquez
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Patent number: 7195761Abstract: A method to treat conditions characterized by formation of amyloid plaques both prophylactically and therapeutically is described. The method employs humanized antibodies which sequester soluble A? peptide from human biological fluids or which preferably specifically bind an epitope contained within position 13–28 of the amyloid beta peptide A?.Type: GrantFiled: August 22, 2002Date of Patent: March 27, 2007Assignees: Eli Lilly and Company, Washington UniversityInventors: David M. Holtzman, Ronald DeMattos, Kelly R. Bales, Steven M. Paul, Naoya Tsurushita, Maximiliano Vasquez
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Patent number: 6703365Abstract: The present invention provides novel complexes consisting of certain GLP-1 molecules associated with a divalent metal cation that is capable of co-precipitating with a GLP-1 molecule. Pharmaceutical compositions and methods of using such complexes for enhancing the expression of insulin in B-type islet cells is claimed, as is a method for treating maturity onset diabetes mellitus in mammals, particularly humans.Type: GrantFiled: April 17, 2002Date of Patent: March 9, 2004Assignee: Eli Lilly and CompanyInventors: John A. Galloway, James A. Hoffmann
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Patent number: 6660716Abstract: Thiazolidinedione (TZD) and its pharmacologically active derivatives can be used in combination with agonists of glucagon-like peptide-1 (GLP-1), to treat non-insulin dependent diabetes mellitus, optionally with other therapies, by improving glycemic control while minimizing side effects, such as heart hypertrophy and elevated fed-state plasma glucose, which are associated with both TZD and GLP-1 monotherapies. Thus, the co-administration of TZD and GLP-1 helps regulate glucose homeostasis in Type II diabetic patients.Type: GrantFiled: April 24, 2001Date of Patent: December 9, 2003Assignee: Eli Lilly and CompanyInventors: Fatima Emitsel Yakubu-Madus, Lawrence Edward Stramm, William Terry Johnson, Vignati Louis
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Patent number: 6583111Abstract: This invention relates the use of glucagon-like peptides such as GLP-1, a GLP-1 analog, or a GLP-1 derivative in methods and compositions for reducing body weight.Type: GrantFiled: June 1, 2000Date of Patent: June 24, 2003Assignee: Eli Lilly and CompanyInventors: Richard DiMarchi, Suad Efendic
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Patent number: 6573237Abstract: The present invention discloses a stable, soluble formulation comprising a medically useful peptide or protein, a hydrophobic preservative, and nicotinamide. Said storage-stable, soluble formulation is useful as a multi-use pharmaceutical product.Type: GrantFiled: June 12, 2002Date of Patent: June 3, 2003Assignee: Eli Lilly and CompanyInventor: Vincent Joseph Rinella, Jr.
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Patent number: 6555521Abstract: The invention provides individual tetragonal flat rod shaped or plate-like crystals of glucagon-like peptide-1 related molecules, processes for their preparation, compositions and methods of use. The crystal preparations exhibit extended time action in vivo and are useful for treating diabetes, obesity and related conditions.Type: GrantFiled: November 30, 2001Date of Patent: April 29, 2003Assignee: Eli Lilly and CompanyInventors: Ronald Norbert Hermeling, James Arthur Hoffmann, Chakravarthy Narasimhan
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Patent number: 6551992Abstract: The present invention provides a monomeric insulin analog formulation stabilized against aggregation in which the buffering agent is either TRIS or arginine. The stable formulations of the present invention are useful for treating diabetes, and are particularly advantageous in treatment regimes requiring lengthy chemical and physical stability, such as, in continuous infusion systems.Type: GrantFiled: November 29, 1999Date of Patent: April 22, 2003Assignee: Eli Lilly and CompanyInventors: Michael Rosario DeFelippis, Michael Allen Dobbins, Bruce Hill Frank, Shun Li, Dawn Marie Rebhun
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Patent number: 6440930Abstract: The present invention discloses a stable, soluble formulation comprising a medically useful peptide or protein, a hydrophobic preservative, and nicotinamide. Said storage-stable, soluble formulation is useful as a multi-use pharmaceutical product.Type: GrantFiled: March 16, 2001Date of Patent: August 27, 2002Assignee: Eli Lilly and CompanyInventor: Vincent Joseph Rinella, Jr.
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Patent number: 6410513Abstract: The present invention provides novel complexes consisting of certain GLP-1 molecules associated with a divalent metal cation that is capable of co-precipitating with a GLP-1 molecule. Pharmaceutical compositions and methods of using such complexes for enhancing the expression of insulin in B-type islet cells is claimed, as is a method for treating maturity onset diabetes mellitus in mammals, particularly humans.Type: GrantFiled: May 18, 2000Date of Patent: June 25, 2002Assignee: Eli Lilly and CompanyInventors: John A. Galloway, James A. Hoffman
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Patent number: 6395509Abstract: The invention includes isolated nucleic acid molecules encoding a Rhesus ob gene product that regulates obesity in mammals. A preferred embodiment consisting of a native DNA sequence is disclosed, as are vectors and methods for expressing the Rhesus ob gene product.Type: GrantFiled: May 26, 1995Date of Patent: May 28, 2002Assignee: Eli Lilly and CompanyInventors: Margret B. Basinski, Brigitte E. Schoner
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Patent number: 6388053Abstract: The present invention provides novel complexes consisting of certain GLP-1 molecules associated with a divalent metal cation that is capable of co-precipitating with a GLP-1 molecule. Pharmaceutical compositions and methods of using such complexes for enhancing the expression of insulin in B-type islet cells is claimed, as is a method for treating maturity onset diabetes mellitus in mammals, particularly humans.Type: GrantFiled: October 12, 2001Date of Patent: May 14, 2002Assignee: Eli Lilly and CompanyInventors: John A. Galloway, James A. Hoffmann
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Patent number: 6380357Abstract: The invention provides individual tetragonal flat rod shaped or plate-like crystals of glucagon-like peptide-1 related molecules, processes for their preparation, compositions and methods of use. The crystal preparations exhibit extended time action in vivo and are useful for treating diabetes, obesity and related conditions.Type: GrantFiled: December 11, 1998Date of Patent: April 30, 2002Assignee: Eli Lilly and CompanyInventors: Ronald Norbert Hermeling, James Arthur Hoffmann, Chakravarthy Narasimhan
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Patent number: 6358924Abstract: Methods and formulations are presented that provide for a) the oral absorption of GLP-1 peptides that bind surfactants; and b) long-term storage of formulations containing these peptides. For example, a GLP-1/DSS complex is administered orally instead of parenterally, which is much more convenient for, and facilitates compliance with diabetic patients and persons with other GLP-1 treated conditions.Type: GrantFiled: June 1, 2000Date of Patent: March 19, 2002Assignee: Eli Lilly and CompanyInventor: James Arthur Hoffmann
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Patent number: 6277819Abstract: This invention provides a method of reducing mortality and morbidity after myocardial infarction. GLP-1, a GLP-1 analog, or a GLP-1 derivative, is administered at a dose effective to normalize blood glucose.Type: GrantFiled: August 21, 1997Date of Patent: August 21, 2001Assignee: Eli Lilly and CompanyInventor: Suad Efendic
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Patent number: 6034054Abstract: The present invention provides a monomeric insulin analog formulation stabilized against aggregation in which the buffering agent is either TRIS or arginine. The stable formulations of the present invention are useful for treating diabetes, and are particularly advantageous in treatment regimes requiring lengthy chemical and physical stability, such as, in continuous infusion systems.Type: GrantFiled: June 11, 1998Date of Patent: March 7, 2000Assignee: Eli Lilly and CompanyInventors: Michael Rosario DeFelippis, Michael Allen Dobbins, Bruce Hill Frank, Shun Li, Dawn Marie Rebhun
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Patent number: 6027911Abstract: The present invention provides the cDNA sequence encoding bovine dipeptidylaminopeptidase 1. The invention demonstrates that bovine DAP 1 coded by a single cDNA. The mature protein is derived from a single polypeptide consisting of a signal peptide, and a major polypeptide which is processed to generate the a subunit, b subunit and g subunit.Type: GrantFiled: April 3, 1998Date of Patent: February 22, 2000Assignee: Eli Lilly and CompanyInventors: Christopher Carl Frye, Charles Lee Hershberger, Haichao Zhang
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Patent number: 5952297Abstract: The present invention discloses various parenteral pharmaceutical formulations having a protracted effect, which comprise: a sterile aqueous suspension of about 20 U/mL to about 500 U/mL insulin analog, about 5 mg/mL to about 10 mg/mL sodium chloride, about 0.2 to about 2.0 mg/mL physiologically acceptable buffer, a zinc ion content of about 0.07 mg/mL to about 0.1 mg/mL, and a physiologically acceptable preservative at a pH of about 6.5 to about 7.8; such that less than 5% of the analog present in the suspension is in the dissolved state.Type: GrantFiled: September 26, 1997Date of Patent: September 14, 1999Assignee: Eli Lilly and CompanyInventors: Michael R. De Felippis, Bruce H. Frank
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Patent number: 5922540Abstract: The invention provides isolated nucleic acid compounds encoding a novel MTG of Staphylococcus aureus. Also provided are vectors and transformed heterologous host cells for expressing the MTG and a method for identifying compounds that bind and/or inhibit the enzymatic activity of the MTG.Type: GrantFiled: December 20, 1996Date of Patent: July 13, 1999Assignee: Eli Lilly and CompanyInventors: Jo Ann Hoskins, Stanley R. Jaskunas, Jr., Robert B. Peery, Paul L. Skatrud