Abstract: Methods for treating a disorder associated with immunoglobulin E (IgE) in a subject with antibodies capable of binding to the C?mx domain of a membrane-bound IgE. The subject can be administered with at least two doses of the antibody, the two doses being at least three months apart.
Abstract: Provided herein are polypeptides which include tenth fibronectin type III domains (10Fn3) that binds to serum albumin. Also provided are fusion molecules comprising a serum albumin binding 10Fn3 joined to a heterologous protein for use in diagnostic and therapeutic applications.
Type:
Grant
Filed:
January 21, 2020
Date of Patent:
September 6, 2022
Assignee:
BRISTOL-MYERS SQUIBB COMPANY
Inventors:
Stanley Richard Krystek, Jr., Tracy S. Mitchell, Michael L. Gosselin, Dasa Lipovsek, Juhi Juneja
Abstract: The present invention provides a humanized antibody or antibody fragment comprising (a) a humanized light chain comprising 1) Complementarity Determining Region (CDR)-L1, the sequence of which is identical to the sequence of SEQ ID NO: 3; 2) CDR-L2, the sequence of which is identical to the sequence of SEQ ID NO: 4; and 3) CDR-L3, the sequence of which is identical to the sequence of SEQ ID NO: 5, and (b) a humanized heavy chain comprising 1) CDR-H1, the sequence of which is identical to the sequence of SEQ ID NO: 6; 2) CDR-H2, the sequence of which is identical to the sequence of SEQ ID NO: 7; and 3) CDR-H3, the sequence of which is identical to the sequence of SEQ ID NO: 8, as well as methods for treating, diagnosing, and monitoring the progression of HIT. The present invention also provides methods for assessing the antigenicity and ability to cause HIT of anionic anticoagulants.
Type:
Grant
Filed:
June 20, 2019
Date of Patent:
September 6, 2022
Assignee:
The Trustees of the University of Pennsylvania
Inventors:
Mark I. Greene, Douglas B. Cines, Zheng Cai, Zhiqiang Zhu
Abstract: The present invention is in the fields of medicinal chemistry, biotechnology and pharmaceuticals. The invention provides compositions comprising one or more collagen mimetic peptides, optionally attached to one or more therapeutic compounds or one or more imaging compounds, for use in methods of treating, preventing, ameliorating, curing and diagnosing certain diseases and physical disorders in humans and veterinary animals, as well as methods of manufacturing such composition. The invention also provides medical devices comprising one or more such compositions of the invention.
Type:
Grant
Filed:
May 20, 2022
Date of Patent:
September 6, 2022
Assignee:
SUSTAIN HOLDINGS, LLC
Inventors:
Richard Eric Schlumpf, Robert Baratta, Shawn A. Delorey
Abstract: Methods and FSP27 compositions for treating and/or preventing metabolic disease and conditions associated insulin resistance, obesity, inflammation and dyslipidemia are described.
Type:
Grant
Filed:
June 14, 2018
Date of Patent:
September 6, 2022
Assignee:
Ohio University
Inventors:
Vishwajeet Puri, John Kopchick, Vishva Sharma
Abstract: The present invention provides immune stimulating peptides (immunorhelins) capable of stimulating GnRH receptors when dosed to human patients or cells. These immunorhelins have utility in treating viral diseases and cancer.
Type:
Grant
Filed:
January 19, 2018
Date of Patent:
September 6, 2022
Assignee:
ISR IMMUNE SYSTEM REGULATION HOLDING AB
Inventors:
Ola Winqvist, Emma Lindh, Robert Wallin, Matt Gregory, Steven Moss
Abstract: The present invention relates to methods of detecting, diagnosing and distinguishing between demyelinating diseases such as Multiple Sclerosis. The present invention also relates to methods of treating, and peptides for use in the treatment of, demyelinating diseases such as Multiple Sclerosis.
Type:
Grant
Filed:
November 1, 2017
Date of Patent:
September 6, 2022
Assignee:
MATN SCIENTIFIC LIMITED
Inventors:
Mahmoud Sedaghati, Mahsa Sedaghati, Tina Sedaghati
Abstract: The present invention provides a family of non-naturally occurring polypeptides having cholesterol efflux activity that parallels that of full-length apolipoproteins (e.g., Apo AI and Apo E), and having high selectivity for ABCA1 that parallels that of full-length apolipoproteins. Further, the peptides of the invention have little or no toxicity when administered at therapeutic and higher doses. The invention also provides compositions comprising such polypeptides, methods of identifying, screening and synthesizing such polypeptides, and methods of treating, preventing or diagnosing diseases and disorders associated with dyslipidemia, hypercholesterolemia, or inflammation; or diseases involving abnormal glucose metabolism, e.g., diabetes, metabolic syndrome; or Alzheimer's Disease or frontotemporal dementia.
Type:
Grant
Filed:
September 10, 2020
Date of Patent:
September 6, 2022
Assignee:
The Regents of the University of California
Inventors:
John K. Bielicki, Jan Johansson, Waleed Danho
Abstract: The present invention relates to a composition comprising a protein phosphatase 1 inhibitory peptide for treating vascular diseases. The composition of the present invention inhibits protein phosphatase 1 (PP1)-mediated dephosphorylation to suppress abnormal proliferation of vascular smooth muscle cells (VSMCs), and activates eNOS of vascular endothelial cells (VECs) to induce the recovery from dysfunction, and thus can be favorably used in the treatment of vascular diseases including pulmonary hypertension.
Abstract: The present invention is in the fields of medicinal chemistry, biotechnology and pharmaceuticals. The invention provides compositions comprising one or more collagen mimetic peptides, optionally attached to one or more therapeutic compounds or one or more imaging compounds, for use in methods of treating, preventing, ameliorating, curing and diagnosing certain diseases and physical disorders in humans and veterinary animals, as well as methods of manufacturing such composition. The invention also provides medical devices comprising one or more such compositions of the invention.
Type:
Grant
Filed:
April 3, 2020
Date of Patent:
August 30, 2022
Assignee:
SUSTAIN HOLDINGS, LLC
Inventors:
Richard Eric Schlumpf, Robert Baratta, Shawn A. Delorey
Abstract: Novel peptide analogs of a ?-defensin have been developed that provide a biphasic effect in treating disseminated fungal disease and/or associated septic shock. These analogs are active at concentrations below those needed to provide a fungicidal effect, and function by initially mobilizing effector cells of the immune system to address the infective organism followed by regulation of the immune system to down regulate the inflammatory response. These novel ?-defensin analogs are protective at concentrations where naturally occurring ?-defensins have no apparent effect, and include a core set of structural and sequence features not found in native ?-defensins.
Type:
Grant
Filed:
June 26, 2020
Date of Patent:
August 30, 2022
Assignee:
THE UNIVERSITY OF SOUTHERN CALIFORNIA
Inventors:
Michael E. Selsted, Dat Q. Tran, Justin B. Schaal, Virginia Basso
Abstract: Compositions comprising a Teneurin C-terminal Associated Peptide—1 (TCAP-1) peptide are described with respect to methods and uses of same for preventing and/or treating post-traumatic stress disorder (“PTSD”).
Type:
Grant
Filed:
October 12, 2018
Date of Patent:
August 30, 2022
Inventors:
David Lovejoy, Robert Stein, Andrew Slee, Garo Armen
Abstract: The invention belongs to the technical field of polypeptide preparation methods, and in particular relates to a high-purity ACTH (human sequence) or analogue and large-scale preparation method thereof. The main steps include: amino acids are coupled from the C-terminal to the N-terminal by Fmoc solid-phase synthesis method to obtain the crude ACTH (human sequence) or analogue peptidyl-resin with protective groups, wherein the reaction temperature of C-15 peptide synthesis is 40-60° C. After cleavge and precipitation, the crude product of ACTH (human sequence) or analogue is obtained, and then the high-purity product is obtained by liquid chromatography. The chromatographic purity of ACTH (human sequence) or analogue prepared by the invention is more than 99%, the stability is good, and the yield of the target peptide is ?63%.
Abstract: Analogues of PYY differing from native human PYY by substitution of Ser23 with Ala23, Glu23, Lys23, Gln23 or AIB23. Further optional features include substitutions at further positions, loss of the Tyr1 residue of native human PYY and amidation of the C-terminus. Suitable for use as pharmaceuticals for treating and preventing disorders, in particular diabetes and obesity.
Abstract: The present disclosure relates to compounds of Formula I being cyclic metabolites of oxytocin. These derivatives have enhanced selectivity for the oxytocin receptor.
Type:
Grant
Filed:
September 27, 2018
Date of Patent:
August 16, 2022
Assignee:
Kinoxis Therapeutics Pty Ltd
Inventors:
Michael Kassiou, Damien Gulliver, Tristan Reekie, Timothy Katte, William Jorgensen, Eryn Werry
Abstract: A method of alleviating joint pain in a patient comprising evaluating the patient's joint pain when undergoing motions associated stress to the joint, and injecting the patient with a peptide of SEQ ID No. 1, and thereafter evaluating the patient's joint pain when undergoing the same motion.
Type:
Grant
Filed:
October 30, 2020
Date of Patent:
August 16, 2022
Assignee:
ORTHOTROPHIX, INC.
Inventors:
Yoshinari Kumagai, Dawn McGuire, Meghan Miller, David Rosen
Abstract: The present invention relates to CNP prodrugs in which the carrier is covalently and reversibly attached to the ring moiety of a CNP moiety, to pharmaceutical compositions comprising such CNP prodrugs, to their uses and to methods of treating diseases that can be treated with the CNP prodrugs of the present invention.
Type:
Grant
Filed:
January 5, 2017
Date of Patent:
August 16, 2022
Assignee:
ASCENDIS PHARMA GROWTH DISORDERS A/S
Inventors:
Harald Rau, Ulrich Hersel, Felix Cleemann, Caroline Elisabeth Rasmussen
Abstract: Methods for enhancing recovery after an ischemic injury, including cerebral ischemia and stroke, by administration of therapeutic amounts of Domain V protein are described.
Type:
Grant
Filed:
December 13, 2018
Date of Patent:
August 16, 2022
Assignee:
University of Kentucky Research Foundation
Abstract: In some aspects, the present invention cell-penetrating compstatin analog and compositions comprising cell-penetrating compstatin analog. In some aspects, the invention further provides methods of using cell-penetrating compstatin analogs treat a complement-mediated disorder, e.g., to inhibit complement-mediated damage to a cell, tissue, or organ, to inhibit production or release of biologically active C3 cleavage products.