EUROPEAN FOUNDATION FOR THE STUDY OF CHRONIC LIVER FAILURE (EF-CLIF) (Espagne)
Inventeur(s)
Arroyo Pérez, Vicente
Moreau, Richard
Claria Enrich, Joan
Fernandez Gomez, Javier
Horrillo Saura, Raquel
Heyn, Holger
Abrégé
The present invention relates to the use of albumin for use in regulating immune cells in a subject in need thereof. The present invention relates particularly to a composition comprising human albumin for use in regulating immune cells in a subject having systemic inflammatory response syndrome.
A61P 7/00 - Médicaments pour le traitement des troubles du sang ou du fluide extracellulaire
A61P 29/00 - Agents analgésiques, antipyrétiques ou anti-inflammatoires non centraux, p. ex. agents antirhumatismauxMédicaments anti-inflammatoires non stéroïdiens [AINS]
2.
BIOMARKERS OF ACUTE-ON-CHRONIC LIVER FAILURE (ACLF) PROGRESSION
EUROPEAN FOUNDATION FOR THE STUDY OF CHRONIC LIVER FAILURE (EF-CLIF) (Espagne)
Inventeur(s)
Arroyo Pérez, Vicente
Moreau, Richard
Claria Enrich, Joan
Fernández Gómez, Javier
Horrillo Saura, Raquel
Lozano Salvatella, Juan José
Aguilar Parera, Ferran
Abrégé
The invention relates to the field of liver diseases and, more in particular, to methods for determining the presence of acute-on chronic liver-failure or methods for determining the risk of a patient suffering from cirrhosis or delayed pre-ACLF of developing ACLF. The invention also relates to methods for distinguishing patients suffering from compensated cirrhosis, acutely decompensated cirrhosis (ADC) or delayed ACLF from patients suffering from early ACLF or ACLF 1, 2, 3, methods for determining the degree of systemic inflammation and methods for determining the presence of a bacterial infection with sepsis.
C12Q 1/6883 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes pour les maladies provoquées par des altérations du matériel génétique
3.
METHOD FOR PRODUCING A LYOPHILIZED COMPOSITION COMPRISING POLYCLONAL IGM AND COMPOSITION OBTAINED
A lyophilized composition including polyclonal immunoglobulin M (IgM), including the steps of: a) providing an initial aqueous solution including IgM at a concentration between about 10 mg/mL and about 50 mg/mL, the polyclonal IgM being at least about 90% by weight of the total protein content of the composition; b) adding amino acids selected from the group consisting of proline, glycine, alanine, valine and hydroxyproline or a mixture thereof at a final concentration of about 0.15 M to about 0.45 M; polysorbate 80 (PS80) at a concentration between about 50 and about 200 ppm; and succinic acid at a concentration between about 1 mM and about 20 mM; and c) lyophilizing the IgM composition obtained in step b); wherein the lyophilized composition has a content of pentameric IgM higher than about 90% of the total IgM content, a content of IgM aggregates of less than about 1.5%.
C07K 16/06 - Immunoglobulines, p. ex. anticorps monoclonaux ou polyclonaux provenant de sérum
A61K 9/19 - Préparations médicinales caractérisées par un aspect particulier à l'état particulaire, p. ex. poudres lyophilisées
A61K 47/18 - AminesAmidesUréesComposés d’ammonium quaternaireAcides aminésOligopeptides ayant jusqu’à cinq acides aminés
A61K 47/22 - Composés hétérocycliques, p. ex. acide ascorbique, tocophérol ou pyrrolidones
A61K 47/26 - Hydrates de carbone, p. ex. polyols ou sucres alcoolisés, sucres aminés, acides nucléiques, mono-, di- ou oligosaccharidesLeurs dérivés, p. ex. polysorbates, esters d’acide gras de sorbitan ou glycyrrhizine
4.
METHOD FOR PRODUCING A LYOPHILIZED COMPOSITION COMPRISING POLYCLONAL IGM AND COMPOSITION OBTAINED
A lyophilized composition including polyclonal immunoglobulin M (IgM), including the steps of: a) providing an initial aqueous solution including IgM at a concentration between about 10 mg/mL and about 50 mg/mL, the polyclonal IgM being at least about 90% by weight of the total protein content of the composition; b) adding amino acids selected from the group consisting of proline, glycine, alanine, valine and hydroxyproline or a mixture thereof at a final concentration of about 0.15 M to about 0.45 M; polysorbate 80 (PS80) at a concentration between about 50 and about 200 ppm; and succinic acid at a concentration between about 1 mM and about 20 mM; and c) lyophilizing the IgM composition obtained in step b); wherein the lyophilized composition has a content of pentameric IgM higher than about 90% of the total IgM content, a content of IgM aggregates of less than about 1.5%.
A61K 39/395 - AnticorpsImmunoglobulinesImmunsérum, p. ex. sérum antilymphocitaire
A61K 47/18 - AminesAmidesUréesComposés d’ammonium quaternaireAcides aminésOligopeptides ayant jusqu’à cinq acides aminés
A61K 47/26 - Hydrates de carbone, p. ex. polyols ou sucres alcoolisés, sucres aminés, acides nucléiques, mono-, di- ou oligosaccharidesLeurs dérivés, p. ex. polysorbates, esters d’acide gras de sorbitan ou glycyrrhizine
C07K 16/00 - Immunoglobulines, p. ex. anticorps monoclonaux ou polyclonaux
C07K 16/06 - Immunoglobulines, p. ex. anticorps monoclonaux ou polyclonaux provenant de sérum
5.
Method of treatment of hypoxia inducible factor (HIF)-related conditions
The present invention relates to methods of treatment of Hypoxia Inducible Factor (HIF)-related conditions, and in particular to methods of treatment of HIF-related conditions comprising the administration of a composition comprising transferrins.
A61K 31/472 - Isoquinoléines non condensées, p. ex. papavérine
A61K 45/06 - Mélanges d'ingrédients actifs sans caractérisation chimique, p. ex. composés antiphlogistiques et pour le cœur
A61P 9/10 - Médicaments pour le traitement des troubles du système cardiovasculaire des maladies ischémiques ou athéroscléreuses, p. ex. médicaments antiangineux, vasodilatateurs coronariens, médicaments pour le traitement de l'infarctus du myocarde, de la rétinopathie, de l'insuffisance cérébro-vasculaire, de l'artériosclérose rénale
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
Methods and compositions for treating and/or preventing disease are described. The compositions used in the methods include fractions and subfractions of blood plasma derived from donors, with efficacy in treating and/or preventing diseases both of the central nervous system and peripheral organs and tissues. Methods of manufacturing the compositions are also described.
A61P 3/10 - Médicaments pour le traitement des troubles du métabolisme de l'homéostase du glucose de l'hyperglycémie, p. ex. antidiabétiques
A61P 9/10 - Médicaments pour le traitement des troubles du système cardiovasculaire des maladies ischémiques ou athéroscléreuses, p. ex. médicaments antiangineux, vasodilatateurs coronariens, médicaments pour le traitement de l'infarctus du myocarde, de la rétinopathie, de l'insuffisance cérébro-vasculaire, de l'artériosclérose rénale
A61P 1/16 - Médicaments pour le traitement des troubles du tractus alimentaire ou de l'appareil digestif des troubles de la vésicule biliaire ou du foie, p. ex. protecteurs hépatiques, cholagogues, cholélitholytiques
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
The present invention refers to the use of a biomarker for measuring the efficacy or effectiveness of treatments for neurodegenerative diseases, in particular, for Alzheimer's disease.
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
8.
METHOD FOR PRODUCING HUMAN PLASMA-DERIVED FACTOR VIII / VON WILLEBRAND FACTOR AND COMPOSITION OBTAINED
The present invention refers to a new method for producing a lyophilized pharmaceutical composition comprising human plasma-derived Factor Vlll/Von Willebrand Factor (FVIII/VWF) complex, comprising the steps of: a) providing an initial aqueous solution comprising FVIII/VWF with at least (90) III of FVIII per mg of total proteins, with a ratio of VWF/FVIII activity of at least 0.7; b) adding arginine, histidine, and human serum albumin (HAS); c) lyophilizing the FVIII/VWF solution obtained in step b); and d) reconstituting the lyophilized FVIII/VWF in water for injection thereby obtaining a therapeutic product adequate for the treatment of Hemophilia A and Von Willebrand Disease, wherein prior to administration to a patient, arginine is at a concentration between (42) and (98) mmol/L, histidine is at a concentration between (10) and (24) mmol/L, and albumin is at a concentration between (1) and (2.5) % (w/v), FVIII potency and VWF potency are equal to or higher than 200 ILI/mL, and the obtained product has a FVIII dose up to 3600 IU/vial and a VWF dose up to 5040 lll/vial.
Methods of preparation of therapeutic blood products from pooled plasma donors are described. The therapeutic blood products include, for example, blood plasma, blood plasma proteins, and blood plasma fractions with improved safety through the reduction in concentration or elimination of donor autoantibodies to FcεRIβ.
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
11.
MACHINE FOR THE PREPARATION OF PHARMACEUTICAL PRODUCTS
A machine for the preparation of pharmaceutical products in a sterile environment, including at least two stations of a line for preparing pharmaceutical products and automatic transport means for containers of pharmaceutical products, wherein the machine includes a robot positioned inside the machine and robot control means, the robot being a robotic arm which includes movement means for accessing the stations of the machine.
B25J 5/02 - Manipulateurs montés sur roues ou sur support mobile se déplaçant le long d'un chemin de guidage
B65B 3/00 - Emballage de matériaux plastiques, de semi-liquides, de liquides ou de liquides et solides mélangés, dans des réceptacles ou récipients individuels, p. ex. dans des sacs ou sachets, boîtes, cartons, bidons ou pots
B65B 7/28 - Fermeture de réceptacles ou récipients semi-rigides ou rigides, non déformés par le contenu ou n'en prenant pas la forme, p. ex. boîtes ou cartons en appliquant des fermetures séparées préformées, p. ex. couvercles, capuchons
B65B 43/46 - Alimentation ou positionnement des sacs, boîtes ou cartons en position dilatée, ouverte ou deboutAlimentation des réceptacles préformés rigides, p. ex. boîtes en fer-blanc, capsules, tubes en verre, flacons, vers la position d'empaquetageMise en place des réceptacles ou récipients au poste de remplissageMaintien des réceptacles ou récipients pendant le remplissage en se servant de griffes
B65B 55/02 - Stérilisation, p. ex. de paquets finis
Methods and compositions for the treatment of wounds and ulcers in patients, in particular those patients suffering from chronic, non-healing wounds and ulcers. Fibrinogenases, such as plasmin show utility in decreasing plasma and or blood viscosity resulting in improved wound and ulcer healing in patients. The fibrinogenase may be one selected from the group consisting of an α-fibrinogenase, a β-fibrinogenase, a γ-fibrinogenase, a metallo-α-fibrinogenase, allium-α-fibrinogenase, a plasmin, and combination thereof.
A61K 38/48 - Hydrolases (3) agissant sur des liaisons peptidiques (3.4)
A61P 17/02 - Médicaments pour le traitement des troubles dermatologiques pour traiter les blessures, les ulcères, les brûlures, les cicatrices, les cheloïdes, ou similaires
A method for obtaining Alpha-1 Proteinase Inhibitor for obtaining highly-concentrated Alpha-1 Proteinase Inhibitor (A1PI) includes preparing a solution of A1PI by concentrating an initial solution of A1PI by tangential flow filtration (TFF) against water. The final concentration of A1PI in the concentrated solution is at least 110 mg/ml. The TFF can be carried out against water for injection (WFD).
A composition including human albumin at a concentration between 5% (w/v) and 25% (w/v) is for the treatment of a cognitive impairment by conventional therapeutic plasma exchange (TPE) and low-volume plasma exchange (LVPE) in a patient in need thereof. The patient has a Mini Mental State Examination (MMSE) greater or equal to 15.
A61M 1/34 - Filtration du sang à travers une membrane pour en éliminer une matière, c.-à-d. hémofiltration, diafiltration
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
15.
LIQUID COMPOSITION COMPRISING FACTOR VIII OR FACTOR VIII/VON WILLEBRAND FACTOR COMPLEX
A liquid composition comprising Factor VIII or Factor VIII/von Willebrand Factor complex comprising one or more stabilizers selected from glycerol, sorbitol, sucrose, trehalose, betaine, proline, arginine, histidine, NaCl, calcium, surfactants, antithrombin III, heparin, and albumin, wherein the content of proteases is 30 ng/1,000 FVIII IU or less, wherein osmolality of said composition is between 350 and 800 mOsmol/kg.
A61K 38/36 - Facteurs de coagulation sanguine ou de fibrinolyse
A61K 47/10 - AlcoolsPhénolsLeurs sels, p. ex. glycérolPolyéthylène glycols [PEG]PoloxamèresAlkyléthers de PEG/POE
A61K 47/18 - AminesAmidesUréesComposés d’ammonium quaternaireAcides aminésOligopeptides ayant jusqu’à cinq acides aminés
A61K 47/22 - Composés hétérocycliques, p. ex. acide ascorbique, tocophérol ou pyrrolidones
A61K 47/26 - Hydrates de carbone, p. ex. polyols ou sucres alcoolisés, sucres aminés, acides nucléiques, mono-, di- ou oligosaccharidesLeurs dérivés, p. ex. polysorbates, esters d’acide gras de sorbitan ou glycyrrhizine
C07K 1/22 - Chromatographie d'affinité ou techniques analogues basées sur des procédés d'absorption sélective
16.
USE OF ALBUMIN FOR THE TREATMENT OF DEFECTIVE B-CELL FUNCTION
EUROPEAN FOUNDATION FOR THE STUDY OF CHRONIC LIVER FAILURE (EF-CLIF) (Espagne)
Inventeur(s)
Arroyo Perez, Vicente
Moreau, Richard
Claria Enrich, Joan
Fernandez Gomez, Javier
Nunez Domenech, Laura
Horrillo Saura, Raquel
Abrégé
Use of albumin for the treatment of defective B-cell function
Use of albumin for the treatment of defective B-cell function
The present invention refers to a composition comprising human albumin for regulating B-cell function in a patient suffering from systemic inflammatory response syndrome, in which the albumin is administered to the patient in a dose sufficient to increase B-cell Receptor density in a B-cell population.
A61P 1/16 - Médicaments pour le traitement des troubles du tractus alimentaire ou de l'appareil digestif des troubles de la vésicule biliaire ou du foie, p. ex. protecteurs hépatiques, cholagogues, cholélitholytiques
A61P 37/06 - Immunosuppresseurs, p. ex. médicaments pour le traitement du rejet de greffe
17.
HYPERIMMUNE GLOBULIN COMPOSITIONS FOR USE IN THE TREATMENT OF COVID-19
The disclosure relates to a pharmaceutical composition comprising human plasma-derived polyclonal, anti-SARS-CoV-2 hyperimmune globulins and to said pharmaceutical composition for use in the treatment of a SARS-CoV-2 Omicron variant infection. The disclosure also relates to a method for the preparation of a polyclonal, hyperimmune globulin composition anti-SARS-CoV-2.
Alpha-1-antitrypsin can be used as a therapeutic agent in patients that have suffered neural cell injury arising from traumatic or non-traumatic causes such as an ischemic stroke, cerebral hypoxia or spinal cord injuries. Alpha-1-antitrypsin can also be used in the treatment of neuropathic pain and the promotion of spinal cord revascularization following injury. Compositions including alpha-1 antitrypsin can be administered parenterally or by inhalation to the patients as part of a dosing regimen.
A61K 38/40 - Transferrines, p. ex. lactoferrines, ovotransferrines
A61K 38/57 - Inhibiteurs de protéases provenant d'animauxInhibiteurs de protéases provenant d'humains
A61P 25/02 - Médicaments pour le traitement des troubles du système nerveux des neuropathies périphériques
A61P 25/04 - Analgésiques centraux, p. ex. opioïdes
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
A device is for cooling plasma for a center for collecting plasma by plasmapheresis. The device includes a casing with at least one cooling chamber in the its interior. The chamber includes housings for cooling containers. The device also includes a refrigeration system arranged to refrigerate the chamber, and a control system for the refrigeration system. The refrigeration system and the control system are configured to control the temperature inside the device so as to allow the containers to be cooled to at least −30° C. in 60 minutes or less. The device includes at least two separate chambers contained in the casing, with each of the chambers including housings for bottles of plasma. The refrigeration system is arranged to refrigerate both chambers independently and the control system is configured to control the refrigeration of both chambers separately.
A method of treating a mild and moderate Alzheimer's Disease (AD), including conducting a low-volume plasma exchange (LVPE) to a subject suffering from the mild and moderate Alzheimer's Disease (AD); and administering an effective amount of a composition including human albumin at a concentration between 5% (w/v) and 25% (w/v) to the subject during the LVPE to replace with a subject's plasma. Use of low volume plasma exchange for the treatment of Alzheimer's Disease in early and middle stages. A composition including human albumin at a concentration between 5% (w/v) and 25% (w/v) for the treatment of mild and moderate Alzheimer's Disease (AD) by low-volume plasma exchange (LVPE).
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
01 - Produits chimiques destinés à l'industrie, aux sciences ainsi qu'à l'agriculture
05 - Produits pharmaceutiques, vétérinaires et hygièniques
Produits et services
Chemical preparations for scientific purposes; chemical preparations for supplementation of fibrinogen not for medical or veterinary use; Biological agents for industrial and scientific purposes made from human blood, blood plasma or blood serum, namely, proteins and protein preparations in the nature of albumin, immune globulins and fibrinogen; Biological agents for industrial and scientific purposes, namely, blood-derived proteins in the nature of coagulation factors; Biological agents for commercial and industrial purposes, namely, blood-derived plasma and blood serum sample preparations Pharmaceutical, medical and veterinary preparations for the treatment congenital and acquired fibrinogen deficiency; blood substitutes and blood plasma substitutes for human use; blood serum and blood serum proteins made from human blood for medical use; coagulants made from human blood plasma for medical use; fibrinogen, fibrinogen made from human blood plasma for medical use; pharmaceutical preparations for use in treating blood diseases and for use in medical transplants and oncology; veterinary preparations for treating blood diseases; pharmaceutical preparations for use in blood coagulation
01 - Produits chimiques destinés à l'industrie, aux sciences ainsi qu'à l'agriculture
05 - Produits pharmaceutiques, vétérinaires et hygièniques
Produits et services
Chemical preparations for scientific purposes; chemical preparations for supplementation of fibrinogen not for medical or veterinary use; Biological agents for industrial and scientific purposes made from human blood, blood plasma or blood serum, namely, proteins and protein reparations in the nature of albumin, immune globulins and fibrinogen; Biological agents for industrial and scientific purposes, namely, blood-derived proteins in the nature of coagulation factors; Biological agents for commercial and industrial purposes, namely, blood-derived plasma and blood serum sample preparations Pharmaceutical, medical and veterinary preparations for the treatment congenital and acquired fibrinogen deficiency; blood substitutes and blood plasma substitutes for human use; blood serum and blood serum proteins made from human blood for medical use; coagulants made from human blood plasma for medical use; fibrinogen, fibrinogen made from human blood plasma for medical use; pharmaceutical preparations for use in treating blood diseases and for use in medical transplants and oncology; veterinary preparations for treating blood diseases; pharmaceutical preparations for use in blood coagulation
01 - Produits chimiques destinés à l'industrie, aux sciences ainsi qu'à l'agriculture
05 - Produits pharmaceutiques, vétérinaires et hygièniques
Produits et services
(1) Chemical products for commercial or scientific purposes; biological agents for commercial and scientific purposes, namely, proteins and protein preparations made from human blood, blood plasma or blood serum; biological agents for commercial and scientific purposes, namely, coagulation factors; biological agents for commercial and scientific purposes, namely, plasma and serum preparations
(2) Pharmaceutical products, medical and veterinary preparations; blood substitute, and blood plasma substitute; serum preparations, in particular, serum proteins and solutions containing the same; proteins and protein preparations made from human blood, blood plasma or blood serum; coagulation factors; fibrinogen, fibrinogen made from human blood plasma; pharmaceutical and veterinary products for hematology, intensive medicine, transplantation medicine, oncology, for influencing blood diseases, for influencing blood coagulation
01 - Produits chimiques destinés à l'industrie, aux sciences ainsi qu'à l'agriculture
05 - Produits pharmaceutiques, vétérinaires et hygièniques
Produits et services
(1) Chemical products for commercial or scientific purposes; biological agents for commercial and scientific purposes, namely, proteins and protein preparations made from human blood, blood plasma or blood serum; biological agents for commercial and scientific purposes, namely, coagulation factors; biological agents for commercial and scientific purposes, namely, plasma and serum preparations
(2) Pharmaceutical products, medical and veterinary preparations; blood substitute, and blood plasma substitute; serum preparations, in particular, serum proteins and solutions containing the same; proteins and protein preparations made from human blood, blood plasma or blood serum; coagulation factors; fibrinogen, fibrinogen made from human blood plasma; pharmaceutical and veterinary products for hematology, intensive medicine, transplantation medicine, oncology, for influencing blood diseases, for influencing blood coagulation
01 - Produits chimiques destinés à l'industrie, aux sciences ainsi qu'à l'agriculture
05 - Produits pharmaceutiques, vétérinaires et hygièniques
Produits et services
(1) Chemical products for commercial or scientific purposes; biological agents for commercial and scientific purposes, namely, proteins and protein preparations made from human blood, blood plasma or blood serum; biological agents for commercial and scientific purposes, namely, coagulation factors; biological agents for commercial and scientific purposes, namely, plasma and serum preparations
(2) Pharmaceutical products, medical and veterinary preparations; blood substitute, and blood plasma substitute; serum preparations, in particular, serum proteins and solutions containing the same; proteins and protein preparations made from human blood, blood plasma or blood serum; coagulation factors; fibrinogen, fibrinogen made from human blood plasma; pharmaceutical and veterinary products for hematology, intensive medicine, transplantation medicine, oncology, for influencing blood diseases, for influencing blood coagulation
A61P 9/10 - Médicaments pour le traitement des troubles du système cardiovasculaire des maladies ischémiques ou athéroscléreuses, p. ex. médicaments antiangineux, vasodilatateurs coronariens, médicaments pour le traitement de l'infarctus du myocarde, de la rétinopathie, de l'insuffisance cérébro-vasculaire, de l'artériosclérose rénale
28.
STABLE PLASMIN COMPOSITIONS FOR ORGAN PRESERVATION AND RECONDITIONING
Disclosed herein are methods and compositions for preserving or reconditioning organs prior to transplant. The compositions of the present invention contain plasmin and/or functionally active mutants thereof formulated in a pharmaceutically acceptable organ preservation solution. The compositions are stable and non-toxic to the organ intended for transplant.
A method for preparing a composition of human plasma-derived immunoglobulin M (IgM) includes PEG precipitation of the IgM, resuspension of the precipitated IgM; (c) performing an adsorption chromatography, removing isoagglutinins A/B, nanofiltration, and ultrafiltration/diafiltration. The precipitation can be performed at a pH between 4.5 and 6.5, and the PEG can be at a concentration between 5 (w/v) and 11% (w/v).
C07K 16/06 - Immunoglobulines, p. ex. anticorps monoclonaux ou polyclonaux provenant de sérum
A61K 39/395 - AnticorpsImmunoglobulinesImmunsérum, p. ex. sérum antilymphocitaire
A61K 47/18 - AminesAmidesUréesComposés d’ammonium quaternaireAcides aminésOligopeptides ayant jusqu’à cinq acides aminés
A61K 47/26 - Hydrates de carbone, p. ex. polyols ou sucres alcoolisés, sucres aminés, acides nucléiques, mono-, di- ou oligosaccharidesLeurs dérivés, p. ex. polysorbates, esters d’acide gras de sorbitan ou glycyrrhizine
A unit for automatically collecting blood and/or plasma, includes a number of stations for automatically collecting blood and/or plasma and at least one venepuncture robot. The robot has a blood vessel detector. The robot is fitted on a linear guide and is movable on the linear guide. The stations are laid out along the linear guide such that the robot can move along the linear guide to access the stations.
Bone Composite and Compositions, particularly multicomponent or multipart compositions, are for the preparation of bone constructs for use in trauma, or cancer patients for example. The multipart compositions are based around combinations of fibrinogen, thrombin, hydrogels and calcium/phosphorous salts. The multipart compositions are capable of being printed to yield bone constructs using a 3D printing process to produce accurate and precise bone constructs of a desired geometry.
A61L 27/44 - Matériaux composites, c.-à-d. en couches ou contenant un matériau dispersé dans une matrice constituée d'un matériau analogue ou différent comportant une matrice macromoléculaire
A61L 27/46 - Matériaux composites, c.-à-d. en couches ou contenant un matériau dispersé dans une matrice constituée d'un matériau analogue ou différent comportant une matrice macromoléculaire avec des charges inorganiques contenant du phosphore
B29C 64/106 - Procédés de fabrication additive n’utilisant que des matériaux liquides ou visqueux, p. ex. dépôt d’un cordon continu de matériau visqueux
Disclosed herein are human blood fractions depleted of disease-causing extracellular vesicles, prepared by plasma exchange, that may find use in the treatment of a condition selected from the group consisting of neurodegenerative disease, autoimmune disease, cardiovascular disease, renal disease, and liver disease. In particular, the depleted blood fractions may find use in treating neurodegenerative diseases such as Parkinson's Disease or Alzheimer's Disease.
A61P 25/00 - Médicaments pour le traitement des troubles du système nerveux
A61P 9/00 - Médicaments pour le traitement des troubles du système cardiovasculaire
A61P 1/16 - Médicaments pour le traitement des troubles du tractus alimentaire ou de l'appareil digestif des troubles de la vésicule biliaire ou du foie, p. ex. protecteurs hépatiques, cholagogues, cholélitholytiques
A61P 13/12 - Médicaments pour le traitement des troubles du système urinaire des reins
A61P 37/00 - Médicaments pour le traitement des troubles immunologiques ou allergiques
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
FUNDACIO PRIVADA INSTITUT D'INVESTIGACIO ONCOLOGICA DE VALL HEBRON (Espagne)
Inventeur(s)
Paez Regadera, Antonio Manuel
Perez Perarnau, Alba
Bravo Camison, Isabel
Tabernero Caturla, Josep
Elez Fernandez, Elena
Villanueva Cardus, Josep
Abrégé
Disclosed herein are human blood fractions depleted of disease-causing extracellular vesicles, prepared by plasma exchange, that may find use in the treatment of a cancer. In particular, the depleted blood fractions may find use in treating KRAS mutant cancers.
05 - Produits pharmaceutiques, vétérinaires et hygièniques
Produits et services
Diagnostic kits comprised of medical diagnostic reagents and nucleic acids for testing blood for detection and analysis of Human Immunodeficiency Type 1 (HIV-1), Human Immunodeficiency Type 2 (HIV-2), Hepatitis C (HCV), Hepatitis B (HBV) and West Nile (WNV) viruses
Compositions include highly concentrated Alpha-1 Proteinase Inhibitor (A1PI) in a concentration greater than or equal to 100 mg/ml. Pharmaceutical compositions can be prepared from these compositions. The pharmaceutical compositions can be suitable for subcutaneous administration. The highly concentrated A1PI solutions can be obtained by single-pass tangential flow filtration (SPTFF).
A61K 47/12 - Acides carboxyliquesLeurs sels ou anhydrides
A61K 47/26 - Hydrates de carbone, p. ex. polyols ou sucres alcoolisés, sucres aminés, acides nucléiques, mono-, di- ou oligosaccharidesLeurs dérivés, p. ex. polysorbates, esters d’acide gras de sorbitan ou glycyrrhizine
A61K 47/30 - Composés macromoléculaires organiques ou inorganiques, p. ex. polyphosphates inorganiques
41.
METHOD FOR THE TREATMENT OF A VIRAL INFECTION WITH HUMAN ALPHA-1 ANTITRYPSIN
A method is for the treatment of a viral infection with human alpha-1 antitrypsin (A1AT). Methods and compositions for the treatment of coronavirus disease 2019 (COVID-19) in a patient, include administering to the patient a therapeutically effective amount of human alpha-1 antitrypsin. The A1AT is administered in an amount between 60 mg/kg and 200 mg/kg. Methods and compositions for the treatment of Cytokine Release Syndrome (CRS) in a patient, include administering to the patient a therapeutically effective amount of an inhibitor of interleukin-6 in combination with a therapeutically effective amount of A1AT.
Pharmaceutical compositions containing transferrin or lactoferrin for use in promoting or inducing the generation new neural cells in a patient that has suffered a neurodegenerative event. The neurodegenerative event may be caused by a neurodegenerative disease such as Alzheimer's, Parkinson's, Huntington's, or amyotrophic lateral sclerosis. Ideally, the transferrin and/or lactoferrin have a low iron saturation.
A61K 38/40 - Transferrines, p. ex. lactoferrines, ovotransferrines
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
Pharmaceutical compositions containing transferrin and, or lactoferrin for use in promoting and or inducing the generation new neural cells in a patient that has suffered a neurodegenerative event arising from at least one of a traumatic brain injury, a non-traumatic brain injury, a spinal cord injury, a peripheral nerve injury, or peripheral neuropathy. Ideally, the transferrin and/or lactoferrin have a low iron saturation.
C07K 14/79 - Transferrines, p. ex. lactoferrines, ovotransferrines
A61K 45/06 - Mélanges d'ingrédients actifs sans caractérisation chimique, p. ex. composés antiphlogistiques et pour le cœur
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
A61K 38/18 - Facteurs de croissanceRégulateurs de croissance
45.
METHOD FOR THE TREATMENT OF VIRUS INFECTION WITH IVIG AND CONVALESCENT PLASMA
Method for the treatment of virus infection with IVIG and convalescent plasma. Methods and compositions for the treatment of coronavirus disease 2019 (COVID-19) in a patient in need thereof, including administering to the patient a therapeutically effective amount of intravenous Immunoglobulin G (IVIG) in an amount of about 0.5 g/kg to about 8 g/kg. Methods and compositions for the treatment of coronavirus disease 2019 (COVID-19) in a patient in need thereof, including administering to the patient a therapeutically effective amount of convalescent anti-SARS-CoV-2 plasma, wherein the convalescent anti-SARS-CoV-2 plasma is treated with methylene blue for pathogen inactivation.
A system for dispensing a liquid in a closed chamber includes at least one rapid transfer port in at least one wall of the closed chamber. In addition, a liquid is dispensed in a closed chamber that includes at least one rapid transfer port in at least one wall of the closed chamber.
B65B 3/00 - Emballage de matériaux plastiques, de semi-liquides, de liquides ou de liquides et solides mélangés, dans des réceptacles ou récipients individuels, p. ex. dans des sacs ou sachets, boîtes, cartons, bidons ou pots
B25J 21/00 - Enceintes à dispositifs de manipulation intégrés
Hyperimmune IgG and/or IgM compositions and method for preparing thereof and method for obtaining hyperimmune human plasma from a donor. A liquid therapeutic hyperimmune globulin composition including human plasma-derived immunoglobulin G (IgG) having antibody titre between 250 and 2,500 per mg/mL of IgG and/or a SARS-CoV-2 neutralization activity (IC50 neutralization titer) between 1.5 and 15 per mg/mL of IgG for use in the treatment of coronavirus disease 2019 (COVID-19) in a patient in need thereof. A liquid therapeutic or prophylactic hyperimmune immunoglobulin composition including human plasma-derived immunoglobulin M (IgM) having a SARS-CoV-2 titre between 2,000 and 17,000 and/or a SARS-CoV-2 neutralization activity (IC50 neutralization titre) between 200 and 70,000, methods for preparing thereof, and the use thereof for the treatment or prophylaxis of COVID-19. A method for obtaining hyperimmune human plasma from a donor for use in the treatment of COVID-19.
A system for the sterile filling of containers for pharmaceutical products, which includes a device for sterilizing containers and a machine for filling sterilized containers, wherein the device for sterilizing containers includes at least one autoclave, and wherein the system includes an automated container-accumulation device and means for automatically transporting the containers sterilized in the autoclave from said autoclave to the container-filling machine via said container-accumulation device.
B65B 55/06 - Stérilisation des enveloppes d'emballage ou récipients avant ou pendant l'emballage par la chaleur
A61L 2/07 - Procédés ou appareils de désinfection ou de stérilisation de matériaux ou d'objets autres que les denrées alimentaires ou les lentilles de contactAccessoires à cet effet utilisant des phénomènes physiques de la chaleur des gaz chauds de la vapeur
A61L 2/24 - Appareils utilisant des opérations programmées ou automatiques
B65B 3/00 - Emballage de matériaux plastiques, de semi-liquides, de liquides ou de liquides et solides mélangés, dans des réceptacles ou récipients individuels, p. ex. dans des sacs ou sachets, boîtes, cartons, bidons ou pots
B65B 7/28 - Fermeture de réceptacles ou récipients semi-rigides ou rigides, non déformés par le contenu ou n'en prenant pas la forme, p. ex. boîtes ou cartons en appliquant des fermetures séparées préformées, p. ex. couvercles, capuchons
49.
COMPOSITION COMPRISING ALBUMIN FOR USE IN THE TREATMENT OF AMYOTROPHIC LATERAL SCLEROSIS (ALS) BY PLASMA EXCHANGE
A composition including albumin for use in the treatment of Amyotrophic Lateral Sclerosis (ALS), wherein the composition is administrated to the patient by plasma exchange using a volume of the composition equivalent to approximately 100% of the volume of plasma withdrawn from the patient, and with a frequency of twice a week the first 3 weeks and once a week for the following 21 weeks, for a total period of 24 weeks.
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
09 - Appareils et instruments scientifiques et électriques
36 - Services financiers, assurances et affaires immobilières
41 - Éducation, divertissements, activités sportives et culturelles
Produits et services
Electronic downloadable publications, namely, brochures, informational flyers and teaching materials for use by medical professionals, patients and caregivers featuring information for the treatment of immuno deficiency disorders Information on financial administration of patient reimbursement programs; providing insurance information for patients diagnosed with immuno deficiency disorders regarding medication access and reimbursement programs and insurance premium and co-pay assistance Educational services, namely, providing training to patients with immune deficiency disorders for self-administration of medication and management of immunoglobulin therapy; providing a website featuring non-downloadable videos in the treatment of immuno deficiency disorders
Embodiments of the present invention provide methods for the treatment or prevention of infection-related immune conditions using compositions comprising IgM.
The present invention refers to a new method for producing a lyophilized pharmaceutical composition comprising human plasma-derived Factor Vlll/Von Willebrand Factor (FVIII/VWF) complex, comprising the steps of: a) providing an initial aqueous solution comprising FVIII/VWF with at least (90) III of FVIII per mg of total proteins, with a ratio of VWF/FVIII activity of at least 0.7; b) adding arginine, histidine, and human serum albumin (HAS); c) lyophilizing the FVIII/VWF solution obtained in step b); and d) reconstituting the lyophilized FVIII/VWF in water for injection thereby obtaining a therapeutic product adequate for the treatment of Hemophilia A and Von Willebrand Disease, wherein prior to administration to a patient, arginine is at a concentration between (42) and (98) mmol/L, histidine is at a concentration between (10) and (24) mmol/L, and albumin is at a concentration between (1) and (2.5) % (w/v), FVIII potency and VWF potency are equal to or higher than 200 ILI/mL, and the obtained product has a FVIII dose up to 3600 lU/vial and a VWF dose up to 5040 lll/vial.
The present invention refers to a new method for producing a lyophilized pharmaceutical composition comprising human plasma-derived Factor Vlll/Von Willebrand Factor (FVIII/VWF) complex, comprising the steps of: a) providing an initial aqueous solution comprising FVIII/VWF with at least (90) III of FVIII per mg of total proteins, with a ratio of VWF/FVIII activity of at least 0.7; b) adding arginine, histidine, and human serum albumin (HAS); c) lyophilizing the FVIII/VWF solution obtained in step b); and d) reconstituting the lyophilized FVIII/VWF in water for injection thereby obtaining a therapeutic product adequate for the treatment of Hemophilia A and Von Willebrand Disease, wherein prior to administration to a patient, arginine is at a concentration between (42) and (98) mmol/L, histidine is at a concentration between (10) and (24) mmol/L, and albumin is at a concentration between (1) and (2.5) % (w/v), FVIII potency and VWF potency are equal to or higher than 200 ILI/mL, and the obtained product has a FVIII dose up to 3600 lU/vial and a VWF dose up to 5040 lll/vial.
The present invention refers to a composition comprising human albumin at a concentration between 5 % (w/v) and 25 % (w/v) for the treatment of a cognitive impairment by conventional therapeutic plasma exchange (TPE) and low volume plasma exchange (LVPE) in a patient in need thereof, wherein said patient has a Mini Mental State Examination (MMSE) greater or equal to 15.
A61M 1/34 - Filtration du sang à travers une membrane pour en éliminer une matière, c.-à-d. hémofiltration, diafiltration
A61M 1/36 - Autre traitement du sang dans une dérivation du système circulatoire naturel, p. ex. adaptation de la température, irradiation
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
59.
USE OF THERAPEUTIC PLASMA EXCHANGE AND LOW VOLUME PLASMA EXCHANGE FOR THE TREATMENT OF A COGNITIVE IMPAIRMENT
The present invention relates to a composition comprising human albumin at a concentration of between 5 % (w/v) and 25 % (w/v) for the treatment of a cognitive impairment by therapeutic plasma exchange (TPE) and low-volume plasma exchange (LVPE) in a patient in need thereof, where said patient has a Mini Mental State Examination (MMSE) greater or equal to 15.
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
A61M 1/36 - Autre traitement du sang dans une dérivation du système circulatoire naturel, p. ex. adaptation de la température, irradiation
60.
LIQUID COMPOSITION COMPRISING FACTOR VIII OR FACTOR VIII/VON WILLEBRAND FACTOR COMPLEX
A liquid composition comprising Factor VIII or Factor VIII/von Willebrand Factor complex comprising one or more stabilizers selected from glycerol, sorbitol, sucrose, trehalose, betaine, proline, arginine, histidine, NaCl, calcium, surfactants, antithrombin III, heparin, and albumin, wherein the content of proteases is 30 ng/1,000 FVIII IU or less, wherein osmolality of said composition is between 350 and 800 mOsmol/kg.
A61K 38/00 - Préparations médicinales contenant des peptides
A61K 47/10 - AlcoolsPhénolsLeurs sels, p. ex. glycérolPolyéthylène glycols [PEG]PoloxamèresAlkyléthers de PEG/POE
A61K 47/18 - AminesAmidesUréesComposés d’ammonium quaternaireAcides aminésOligopeptides ayant jusqu’à cinq acides aminés
A61K 47/26 - Hydrates de carbone, p. ex. polyols ou sucres alcoolisés, sucres aminés, acides nucléiques, mono-, di- ou oligosaccharidesLeurs dérivés, p. ex. polysorbates, esters d’acide gras de sorbitan ou glycyrrhizine
61.
LIQUID COMPOSITION COMPRISING FACTOR VIII OR FACTOR VIII/VON WILLEBRAND FACTOR COMPLEX
A liquid composition comprising Factor VIII or Factor VIII/von Willebrand Factor complex comprising one or more stabilizers selected from glycerol, sorbitol, sucrose, trehalose, betaine, proline, arginine, histidine, NaCl, calcium, surfactants, antithrombin III, heparin, and albumin, wherein the content of proteases is 30 ng/1,000 FVIII IU or less, wherein osmolality of said composition is between 350 and 800 mOsmol/kg.
A61K 38/00 - Préparations médicinales contenant des peptides
A61K 47/10 - AlcoolsPhénolsLeurs sels, p. ex. glycérolPolyéthylène glycols [PEG]PoloxamèresAlkyléthers de PEG/POE
A61K 47/18 - AminesAmidesUréesComposés d’ammonium quaternaireAcides aminésOligopeptides ayant jusqu’à cinq acides aminés
A61K 47/26 - Hydrates de carbone, p. ex. polyols ou sucres alcoolisés, sucres aminés, acides nucléiques, mono-, di- ou oligosaccharidesLeurs dérivés, p. ex. polysorbates, esters d’acide gras de sorbitan ou glycyrrhizine
62.
IN VITRO DIAGNOSTIC METHOD FOR ALZHEIMER'S DISEASE BASED ON THE ALBUMIN REDOX LEVEL IN THE CEREBROSPINAL FLUID
An in vitro method for diagnosing Alzheimer's disease (AD) includes determining the content of mercaptoalbumin (HMA) in a sample of cerebrospinal fluid (CSF), and comparing the content determined with the content of HMA in CSF in healthy subjects. If the HMA content is less than that of the healthy subjects, it is indicative of AD.
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
Device (1) for cooling plasma for a centre for collecting plasma by plasmapheresis, said device comprising a casing comprising at least two separate chambers (5), each of the chambers comprising housings (42, 43) for bottles (9) of plasma; the device also comprising a refrigeration system and a control system, being configured to control the temperature inside the device so as to allow the bottles to be cooled to at least -30°C in 60 minutes or less; wherein the refrigeration system is arranged to refrigerate both chambers independently and the control system is configured to control the refrigeration of both chambers separately. Being able to produce two simultaneous cooling cycles is particularly advantageous in mobile distribution centres. Cooling of the bottles may be made by contact with the housings or by natural convection. A distribution centre comprising such a device, e.g. a mobile distribution centre in form of a motor bus, is also disclosed.
F25D 11/02 - Dispositifs autonomes déplaçables associés à des machines frigorifiques, p. ex. réfrigérateurs ménagers avec compartiments de refroidissement à des températures différentes
64.
USE OF ALBUMIN FOR THE TREATMENT OF DEFECTIVE B-CELL FUNCTION
EUROPEAN FOUNDATION FOR THE STUDY OF CHRONIC LIVER FAILURE (EF-CLIF) (Espagne)
Inventeur(s)
Arroyo Perez, Vicente
Moreau, Richard
Claria Enrich, Joan
Fernandez Gomez, Javier
Nunez Domenech, Laura
Horrillo Saura, Raquel
Abrégé
The present invention relates to a composition comprising human albumin for regulating B-cell function in a patient suffering from systemic inflammatory response syndrome, in which the albumin is administered to the patient in a dose sufficient to increase B-cell receptor density in a B-cell population.
A method for controlling the concentration of an anticoagulant composition added to a donor's plasma during a fixed volume apheresis extraction process involves utilizing a donor's hematocrit (HCT) measurement to determine a ratio of the anticoagulant composition to the donor's uncoagulated blood during the apheresis extraction process. The ratio of the anticoagulant composition to the donor's uncoagulated blood during the apheresis extraction process is additionally determined as a function of the total collection volume and/or the desired volume of the anticoagulant composition.
EUROPEAN FOUNDATION FOR THE STUDY OF CHRONIC LIVER FAILURE (EF-CLIF) (Espagne)
Inventeur(s)
Arroyo Perez, Vicente
Moreau, Richard
Claria Enrich, Joan
Fernandez Gomez, Javier
Nuñez Domenech, Laura
Horrillo Saura, Raquel
Abrégé
The present invention relates to a composition comprising human albumin for regulating B-cell function in a patient suffering from systemic inflammatory response syndrome, in which the albumin is administered to the patient in a dose sufficient to increase B-cell receptor density in a B-cell population.
The present invention relates to the use of alpha-1 antitrypsin as a therapeutic agent in patients who have suffered neural cell injury arising from traumatic or non- traumatic causes, such as an ischemic stroke, cerebral hypoxia or spinal cord injuries. Alpha-1 antitrypsin administered in accordance with the treatment regimen of the present invention may also prove useful in the treatment of neuropathic pain and the promotion of spinal cord revascularisation following injury thereto. Compositions comprising alpha-1 antitrypsin may be administered parenterally or by inhalation to the patients as part of an innovative dosing regimen.
The present invention is related to the use of alpha-1-antitrypsin as a therapeutic agent in patients that have suffered neural cell injury arising from traumatic or non-traumatic causes such as an ischemic stroke, cerebral hypoxia or spinal cord injuries. Alpha-1-antitrypsin administered in accordance with the treatment regimen of the present invention may also find utility in the treatment of neuropathic pain and the promotion of spinal cord revascularisation following injury thereto. Compositions comprising alpha-1 antitrypsin may be administered parenterally or by inhalation to the patients as part of an innovative dosing regimen.
Machine (1) for the preparation of pharmaceutical products in a sterile environment, said machine (1) comprising at least two stations of a line (10) for preparing pharmaceutical products and automatic transport means for containers (5) of pharmaceutical products, wherein the machine (1) comprises a robot (2) positioned inside the machine (1) and means for controlling said robot, said robot (2) being a robotic arm which comprises movement means for accessing the stations of the machine (1).
B25J 21/00 - Enceintes à dispositifs de manipulation intégrés
B65B 3/00 - Emballage de matériaux plastiques, de semi-liquides, de liquides ou de liquides et solides mélangés, dans des réceptacles ou récipients individuels, p. ex. dans des sacs ou sachets, boîtes, cartons, bidons ou pots
B65B 55/02 - Stérilisation, p. ex. de paquets finis
B65B 7/28 - Fermeture de réceptacles ou récipients semi-rigides ou rigides, non déformés par le contenu ou n'en prenant pas la forme, p. ex. boîtes ou cartons en appliquant des fermetures séparées préformées, p. ex. couvercles, capuchons
B65B 57/04 - Dispositifs de commande automatique, de vérification, d'alarme ou de sécurité sensibles à l'absence, à la présence, à l'alimentation anormale ou à la mauvaise présentation du matériau d'attache ou d'emballage des réceptacles ou des paquets et dont le fonctionnement commande ou arrête l'alimentation de ce matériau, de ces réceptacles ou paquets
70.
MACHINE FOR THE PREPARATION OF PHARMACEUTICAL PRODUCTS
Machine (1) for the preparation of pharmaceutical products in a sterile environment, said machine (1) comprising at least two stations of a line (10) for preparing pharmaceutical products and automatic transport means for containers (5) of pharmaceutical products, wherein the machine (1) comprises a robot (2) positioned inside the machine (1) and means for controlling said robot, said robot (2) being a robotic arm which comprises movement means for accessing the stations of the machine (1).
B25J 21/00 - Enceintes à dispositifs de manipulation intégrés
B65B 7/28 - Fermeture de réceptacles ou récipients semi-rigides ou rigides, non déformés par le contenu ou n'en prenant pas la forme, p. ex. boîtes ou cartons en appliquant des fermetures séparées préformées, p. ex. couvercles, capuchons
B65B 55/02 - Stérilisation, p. ex. de paquets finis
B65B 57/04 - Dispositifs de commande automatique, de vérification, d'alarme ou de sécurité sensibles à l'absence, à la présence, à l'alimentation anormale ou à la mauvaise présentation du matériau d'attache ou d'emballage des réceptacles ou des paquets et dont le fonctionnement commande ou arrête l'alimentation de ce matériau, de ces réceptacles ou paquets
71.
Method of treatment of hypoxia inducible factor (HIF)-related conditions
The present invention relates to methods of treatment of Hypoxia Inducible Factor (HIF)-related conditions, and in particular to methods of treatment of HIF-related conditions comprising the administration of a composition comprising transferrins.
A61P 9/10 - Médicaments pour le traitement des troubles du système cardiovasculaire des maladies ischémiques ou athéroscléreuses, p. ex. médicaments antiangineux, vasodilatateurs coronariens, médicaments pour le traitement de l'infarctus du myocarde, de la rétinopathie, de l'insuffisance cérébro-vasculaire, de l'artériosclérose rénale
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
Disclosed herein are methods and compositions for the treatment of wounds and ulcers in patients, in particular those patients suffering from chronic, non-healing wounds and ulcers. Fibrinogenases, such as plasmin show utility in decreasing plasma and or blood viscosity resulting in improved wound and ulcer healing in patients.
A61K 38/48 - Hydrolases (3) agissant sur des liaisons peptidiques (3.4)
A61P 3/10 - Médicaments pour le traitement des troubles du métabolisme de l'homéostase du glucose de l'hyperglycémie, p. ex. antidiabétiques
A61P 9/10 - Médicaments pour le traitement des troubles du système cardiovasculaire des maladies ischémiques ou athéroscléreuses, p. ex. médicaments antiangineux, vasodilatateurs coronariens, médicaments pour le traitement de l'infarctus du myocarde, de la rétinopathie, de l'insuffisance cérébro-vasculaire, de l'artériosclérose rénale
A61P 17/02 - Médicaments pour le traitement des troubles dermatologiques pour traiter les blessures, les ulcères, les brûlures, les cicatrices, les cheloïdes, ou similaires
Disclosed herein are methods and compositions for the treatment of wounds and ulcers in patients, in particular those patients suffering from chronic, non-healing wounds and ulcers. Fibrinogenases, such as plasmin show utility in decreasing plasma and or blood viscosity resulting in improved wound and ulcer healing in patients.
A61K 38/48 - Hydrolases (3) agissant sur des liaisons peptidiques (3.4)
A61P 3/10 - Médicaments pour le traitement des troubles du métabolisme de l'homéostase du glucose de l'hyperglycémie, p. ex. antidiabétiques
A61P 9/10 - Médicaments pour le traitement des troubles du système cardiovasculaire des maladies ischémiques ou athéroscléreuses, p. ex. médicaments antiangineux, vasodilatateurs coronariens, médicaments pour le traitement de l'infarctus du myocarde, de la rétinopathie, de l'insuffisance cérébro-vasculaire, de l'artériosclérose rénale
A61P 17/02 - Médicaments pour le traitement des troubles dermatologiques pour traiter les blessures, les ulcères, les brûlures, les cicatrices, les cheloïdes, ou similaires
Unit for automatically collecting blood and/or plasma, comprising a plurality of stations for automatically collecting blood and/or plasma and at least one venipuncture robot. The robot comprises means for detecting blood vessels. Said robot is mounted on a linear guide and is movable on said linear guide. The stations are distributed along the linear guide such that the robot can move along the linear guide to access said stations.
A61B 5/153 - Dispositifs de prélèvement d'échantillons de sang spécialement adaptés pour le prélèvement d'échantillons de sang veineux ou artériel, p. ex. par des seringues
FUNDACIO INSTITUT D'INVESTIGACIO BIOMEDICA DE BELLVITGE (IDIBELL) (Espagne)
Inventeur(s)
Costa Rierola, Montserrat
Ortiz Fernandez, Ana Maria
Ojosnegros Martos, Samuel
Seriola Petit, Anna
Abrégé
A composition is for improving the culture and implantation of mammalian embryos. The composition includes one or more of the fractions of human plasma fractionation using the Cohn method wherein in the composition human serum albumin (HSA) is between 90% and 96% of the total proteins in the composition, alfa and beta globulins are between 3.5% and 9.99% of the total proteins in the composition, and gamma globulin is between 0.01% and 0.5% of the total proteins in the composition.
Disclosed herein are pharmaceutical compositions containing transferrin and, or lactoferrin for use in promoting and or inducing the generation new neural cells in a patient that has suffered a neurodegenerative event arising from at least one of a traumatic brain injury, a non-traumatic brain injury, a spinal cord injury, a peripheral nerve injury, or peripheral neuropathy. Ideally, the transferrin and/or lactoferrin have a low iron saturation.
A61K 31/00 - Préparations médicinales contenant des ingrédients actifs organiques
A61K 38/17 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains
A61K 38/18 - Facteurs de croissanceRégulateurs de croissance
A61K 38/40 - Transferrines, p. ex. lactoferrines, ovotransferrines
A61P 25/00 - Médicaments pour le traitement des troubles du système nerveux
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
79.
METHOD FOR OBTAINING A COMPOSITION COMPRISING HUMAN PLASMA-DERIVED IMMUNOGLOBULIN M
A method for preparing a composition of human plasma-derived immunoglobulin M (IgM) including the steps of (a) PEG precipitation of the IgM; (b) resuspension of the precipitated IgM; (c) performing an adsorption chromatography; (d) removing isoagglutinins A/B; (e) nanofiltration; and (f) ultrafiltration/diafiltration. In the method for preparing the composition, the precipitation step a) is preferably performed at a pH between 4.5 and 6.5, and the PEG is preferably at a concentration between 5 (w/v) and 11% (w/v).
Disclosed herein are pharmaceutical compositions containing transferrin and, or lactoferrin for use in promoting and or inducing the generation new neural cells in a patient that has suffered a neurodegenerative event arising from at least one of a traumatic brain injury, a non-traumatic brain injury, a spinal cord injury, a peripheral nerve injury, or peripheral neuropathy. Ideally, the transferrin and/or lactoferrin have a low iron saturation.
A61K 31/00 - Préparations médicinales contenant des ingrédients actifs organiques
A61K 38/17 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains
A61K 38/18 - Facteurs de croissanceRégulateurs de croissance
A61K 38/40 - Transferrines, p. ex. lactoferrines, ovotransferrines
A61P 25/00 - Médicaments pour le traitement des troubles du système nerveux
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
81.
COMPOSITIONS HAVING NEUROREGENERATIVE APPLICATIONS
Disclosed herein are pharmaceutical compositions containing transferrin or lactoferrin for use in promoting or inducing the generation new neural cells in a patient that has suffered a neurodegenerative event. The neurodegenerative event may be caused by a neurodegenerative disease such as Alzheimer's, Parkinson's, Huntington's, or amyotrophic lateral sclerosis. Ideally, the transferrin and/or lactoferrin have a low iron saturation.
A61K 31/00 - Préparations médicinales contenant des ingrédients actifs organiques
A61K 38/17 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains
A61K 38/18 - Facteurs de croissanceRégulateurs de croissance
A61K 38/40 - Transferrines, p. ex. lactoferrines, ovotransferrines
A61P 25/00 - Médicaments pour le traitement des troubles du système nerveux
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
A61K 45/06 - Mélanges d'ingrédients actifs sans caractérisation chimique, p. ex. composés antiphlogistiques et pour le cœur
82.
METHOD FOR OBTAINING A COMPOSITION COMPRISING HUMAN PLASMA-DERIVED IMMUNOGLOBULIN M
A method for preparing a composition of human plasma-derived immunoglobulin M (IgM) including the steps of (a) PEG precipitation of the IgM; (b) resuspension of the precipitated IgM; (c) performing an adsorption chromatography; (d) removing isoagglutinins A/B; (e) nanofiltration; and (f) ultrafiltration/diafiltration. In the method for preparing the composition, the precipitation step a) is preferably performed at a pH between 4.5 and 6.5, and the PEG is preferably at a concentration between 5 (w/v) and 11% (w/v).
Disclosed herein are pharmaceutical compositions containing transferrin or lactoferrin for use in promoting or inducing the generation new neural cells in a patient that has suffered a neurodegenerative event. The neurodegenerative event may be caused by a neurodegenerative disease such as Alzheimer's, Parkinson's, Huntington's, or amyotrophic lateral sclerosis. Ideally, the transferrin and/or lactoferrin have a low iron saturation.
A61K 38/40 - Transferrines, p. ex. lactoferrines, ovotransferrines
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
84.
Composition comprising highly-concentrated α1 proteinase inhibitor and method for obtaining thereof
Compositions include highly-concentrated Alpha-1 Proteinase Inhibitor (A1PI) in a concentration greater than or equal to 100 mg/ml. Pharmaceutical compositions can be prepared from these compositions. The pharmaceutical compositions can be suitable for subcutaneous administration. The highly-concentrated A1PI solutions can be obtained by single-pass tangential flow filtration (SPTFF).
A61K 47/12 - Acides carboxyliquesLeurs sels ou anhydrides
A61K 47/26 - Hydrates de carbone, p. ex. polyols ou sucres alcoolisés, sucres aminés, acides nucléiques, mono-, di- ou oligosaccharidesLeurs dérivés, p. ex. polysorbates, esters d’acide gras de sorbitan ou glycyrrhizine
A61K 47/30 - Composés macromoléculaires organiques ou inorganiques, p. ex. polyphosphates inorganiques
85.
HYPERIMMUNE IGG AND/OR IGM COMPOSITIONS AND METHOD FOR PREPARING THEREOF AND METHOD FOR OBTAINING HYPERIMMUNE HUMAN PLASMA FROM A DONOR
The present disclosure refers to a liquid therapeutic hyperimmune globulin composition comprising human plasma-derived immunoglobulin G (IgG) having antibody titre between 250 and 2,500 per mg/mL of IgG and/or a SARS-CoV-2 neutralization activity (IC50 neutralization titer) between 1.5 and 15 per mg/mL of IgG for use in the treatment of coronavirus disease 2019 (COVID-19) in a patient in need thereof. It also refers to a liquid therapeutic or prophylactic hyperimmune immunoglobulin composition comprising human plasma-derived immunoglobulin M (IgM) having a SARS-CoV-2 titre between 2,000 and 17,000 and/or a SARS-CoV-2 neutralization activity (IC50 neutralization titre) between 200 and 70,000, methods for preparing thereof, and the use thereof for the treatment or prophylaxis of COVID-19. Finally, it also refers to a method for obtaining hyperimmune human plasma from a donor for use in the treatment of COVID-19.
The present disclosure refers to a liquid therapeutic hyperimmune globulin composition comprising human plasma-derived immunoglobulin G (IgG) having antibody titre between 250 and 2,500 per mg/mL of IgG and/or a SARS-CoV-2 neutralization activity (IC50 neutralization titer) between 1.5 and 15 per mg/mL of IgG for use in the treatment of coronavirus disease 2019 (COVID-19) in a patient in need thereof. It also refers to a liquid therapeutic or prophylactic hyperimmune immunoglobulin composition comprising human plasma-derived immunoglobulin M (IgM) having a SARS-CoV-2 titre between 2,000 and 17,000 and/or a SARS-CoV-2 neutralization activity (IC50 neutralization titre) between 200 and 70,000, methods for preparing thereof, and the use thereof for the treatment or prophylaxis of COVID-19. Finally, it also refers to a method for obtaining hyperimmune human plasma from a donor for use in the treatment of COVID-19.
Method for the treatment of a viral infection with human alpha-1 antitrypsin The present invention relates to method and compositions for the treatment of coronavirus disease 2019 (COVID-19) in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of human alpha-1 antitrypsin, wherein A1AT is administered in an amount between 60 mg/kg and 200 mg/kg. The present invention also refers to methods and compositions for the treatment of Cytokine Release Syndrome (CRS) in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of an inhibitor of interleukin-6 in combination with a therapeutically effective amount of A1AT.
A61K 38/57 - Inhibiteurs de protéases provenant d'animauxInhibiteurs de protéases provenant d'humains
A61K 39/395 - AnticorpsImmunoglobulinesImmunsérum, p. ex. sérum antilymphocitaire
A61P 29/00 - Agents analgésiques, antipyrétiques ou anti-inflammatoires non centraux, p. ex. agents antirhumatismauxMédicaments anti-inflammatoires non stéroïdiens [AINS]
A61P 43/00 - Médicaments pour des utilisations spécifiques, non prévus dans les groupes
The present disclosure refers to methods and compositions for the treatment of coronavirus disease 2019 (COVID-19) in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of intravenous Immunoglobulin G (IVIG) in an amount of about 0.5 g/kg to about 8 g/kg. The present disclosure also refers to methods and compositions for the treatment of coronavirus disease 2019 (COVID-19) in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of convalescent anti-SARS-CoV-2 plasma, wherein the convalescent anti-SARS-CoV-2 plasma is treated with methylene blue for pathogen inactivation.
The invention relates to a system for the sterile filling of containers for pharmaceutical products, which comprises a device for sterilising containers and a machine for filling sterilised containers, wherein the device for sterilising containers comprises at least one autoclave, and wherein the system comprises an automated container-accumulation device and means for automatically transporting the containers sterilised in the autoclave from said autoclave to the container-filling machine via said container-accumulation device.
A61L 2/07 - Procédés ou appareils de désinfection ou de stérilisation de matériaux ou d'objets autres que les denrées alimentaires ou les lentilles de contactAccessoires à cet effet utilisant des phénomènes physiques de la chaleur des gaz chauds de la vapeur
A61L 2/00 - Procédés ou appareils de désinfection ou de stérilisation de matériaux ou d'objets autres que les denrées alimentaires ou les lentilles de contactAccessoires à cet effet
91.
SYSTEM AND METHOD FOR THE STERILE FILLING OF CONTAINERS
The invention relates to a system for the sterile filling of containers for pharmaceutical products, which comprises a device for sterilising containers and a machine for filling sterilised containers, wherein the device for sterilising containers comprises at least one autoclave, and wherein the system comprises an automated container-accumulation device and means for automatically transporting the containers sterilised in the autoclave from said autoclave to the container-filling machine via said container-accumulation device.
A61L 2/07 - Procédés ou appareils de désinfection ou de stérilisation de matériaux ou d'objets autres que les denrées alimentaires ou les lentilles de contactAccessoires à cet effet utilisant des phénomènes physiques de la chaleur des gaz chauds de la vapeur
92.
COMPOSITION COMPRISING ALBUMIN FOR USE IN THE TREATMENT OF AMYOTROPHIC LATERAL SCLEROSIS (ALS) BY PLASMA EXCHANGE
The present invention relates to a composition comprising albumin for use in the treatment of Amyotrophic Lateral Sclerosis (ALS), wherein the composition is administrated to the patient by plasma exchange using a volume of said composition equivalent to approximately 100 % of the volume of plasma withdrawn from the patient, and with a frequency of twice a week the first 3 weeks and once a week for the following 21 weeks, for a total period of 24 weeks.
A61M 1/34 - Filtration du sang à travers une membrane pour en éliminer une matière, c.-à-d. hémofiltration, diafiltration
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
93.
COMPOSITION COMPRISING ALBUMIN FOR USE IN THE TREATMENT OF AMYOTROPHIC LATERAL SCLEROSIS (ALS) BY PLASMA EXCHANGE
The present invention relates to a composition comprising albumin for use in the treatment of Amyotrophic Lateral Sclerosis (ALS), wherein the composition is administrated to the patient by plasma exchange using a volume of said composition equivalent to approximately 100 % of the volume of plasma withdrawn from the patient, and with a frequency of twice a week the first 3 weeks and once a week for the following 21 weeks, for a total period of 24 weeks.
A61M 1/34 - Filtration du sang à travers une membrane pour en éliminer une matière, c.-à-d. hémofiltration, diafiltration
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p. ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
94.
SYSTEM AND METHOD FOR DISPENSING A LIQUID INTO A CLOSED ENCLOSURE
The present invention discloses a system for dispensing a liquid into a closed enclosure comprising at least one rapid transfer port in at least one wall of said enclosure. Additionally, the present invention also discloses a method for dispensing a liquid into an enclosure comprising at least one rapid transfer port in at least one wall of said enclosure.
B65B 3/00 - Emballage de matériaux plastiques, de semi-liquides, de liquides ou de liquides et solides mélangés, dans des réceptacles ou récipients individuels, p. ex. dans des sacs ou sachets, boîtes, cartons, bidons ou pots
B67C 3/22 - Mise en bouteilles de liquides ou de semi-liquidesRemplissage des bocaux ou bidons avec des liquides ou semi-liquides en utilisant des appareils de mise en bouteilles ou des appareils analogues Détails
B01L 3/00 - Récipients ou ustensiles pour laboratoires, p. ex. verrerie de laboratoireCompte-gouttes
95.
SYSTEM AND METHOD FOR DISPENSING A LIQUID IN A CLOSED CHAMBER
The present invention relates to a system for dispensing a liquid in a closed chamber which comprises at least one rapid transfer port in at least one wall of said closed chamber. In addition, the present invention also relates to a method of dispensing a liquid in a closed chamber which comprises at least one rapid transfer port in at least one wall of said closed chamber.
B25J 21/00 - Enceintes à dispositifs de manipulation intégrés
B65B 3/00 - Emballage de matériaux plastiques, de semi-liquides, de liquides ou de liquides et solides mélangés, dans des réceptacles ou récipients individuels, p. ex. dans des sacs ou sachets, boîtes, cartons, bidons ou pots
B67C 3/22 - Mise en bouteilles de liquides ou de semi-liquidesRemplissage des bocaux ou bidons avec des liquides ou semi-liquides en utilisant des appareils de mise en bouteilles ou des appareils analogues Détails
Methods for obtaining highly-concentrated Alpha- 1 Proteinase Inhibitor (A1 PI) comprising a step of preparing a solution of A1 PI by concentrating an initial solution of A1 PI by tangential flow filtration (TFF) against water wherein the final concentration of A1 PI in the concentrated solution is at least 110 mg/ml.
Methods for obtaining highly-concentrated Alpha- 1 Proteinase Inhibitor (A1 PI) comprising a step of preparing a solution of A1 PI by concentrating an initial solution of A1 PI by tangential flow filtration (TFF) against water wherein the final concentration of A1 PI in the concentrated solution is at least 110 mg/ml.
Disclosed herein are multicomponent or multipart compositions for the preparation of bone constructs for use of trauma, or cancer patients for example. The multipart compositions are based around innovative combinations of fibrinogen, thrombin, hydrogels and calcium/phosphorous salts. Advantageously, the multipart compositions are capable of being printed to yield bone constructs using a 3D printing process to produce accurate and precise bone constructs of a desired geometry.
A61L 27/44 - Matériaux composites, c.-à-d. en couches ou contenant un matériau dispersé dans une matrice constituée d'un matériau analogue ou différent comportant une matrice macromoléculaire
A61L 27/46 - Matériaux composites, c.-à-d. en couches ou contenant un matériau dispersé dans une matrice constituée d'un matériau analogue ou différent comportant une matrice macromoléculaire avec des charges inorganiques contenant du phosphore
Disclosed herein are multicomponent or multipart compositions for the preparation of bone constructs for use of trauma, or cancer patients for example. The multipart compositions are based around innovative combinations of fibrinogen, thrombin, hydrogels and calcium/phosphorous salts. Advantageously, the multipart compositions are capable of being printed to yield bone constructs using a 3D printing process to produce accurate and precise bone constructs of a desired geometry.
A61L 27/44 - Matériaux composites, c.-à-d. en couches ou contenant un matériau dispersé dans une matrice constituée d'un matériau analogue ou différent comportant une matrice macromoléculaire
A61L 27/46 - Matériaux composites, c.-à-d. en couches ou contenant un matériau dispersé dans une matrice constituée d'un matériau analogue ou différent comportant une matrice macromoléculaire avec des charges inorganiques contenant du phosphore