Patents by Inventor Giuseppe Penna

Giuseppe Penna has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Publication number: 20230381291
    Abstract: The present invention provides antigen presenting cells (APC) carrying human tumor-associated peptides on the cell surface as well as immunogenic compositions including the tumor-associated peptides and/or the antigen presenting cells according to the invention. The immunogenic composition of the invention is useful as a vaccine in the prevention and/or treatment of a tumor disease, particularly melanoma and melanoma residual disease.
    Type: Application
    Filed: July 8, 2021
    Publication date: November 30, 2023
    Applicants: HUMANITAS MIRASOLE S.P.A., HUMANITAS UNIVERSITY, ISTITUTO EUROPEO DI ONCOLOGIA S.R.L.
    Inventors: Maria RESCIGNO, Alessia MELACARNE, Giuseppe PENNA
  • Publication number: 20220370608
    Abstract: The present invention relates to a suppressor or inhibitor of the expression and/or the activity of Chitinase 3-like 1 (CHI3L1) for use in the prevention and/or treatment of tumors, wherein said tumors are resistant to antibody-dependent cell-mediated cytotoxicity (ADCC) dependent therapies and/or for use in reducing the risk of developing resistance to antibody-dependent cell-mediated cytotoxicity (ADCC) dependent therapies.
    Type: Application
    Filed: July 22, 2020
    Publication date: November 24, 2022
    Inventors: Giuseppe PENNA, Maria RESCIGNO, Abbass DARWICH
  • Publication number: 20210052678
    Abstract: The present invention refers to a composition containing a) a fermented supernatant, or fractions thereof, of Lactobacillus casei or paracasei species, the species being characterized by having in their DNA genome at least one DNA sequence essentially identical to one of the sequence selected from the group consisting of: SEQ ID No 1 to 5, and b) proper carriers and/or diluents and/or excipients. The fermented supernatant is obtainable through a method characterized by the fermentation of the Lactobacillus casei or paracasei species in a minimum solution additioned with prebiotic fibers. The fermented supernatant does not have prebiotic fibers.
    Type: Application
    Filed: February 4, 2019
    Publication date: February 25, 2021
    Applicant: POSTBIOTiCA S.R.L.
    Inventors: Maria RESCIGNO, Giuseppe PENNA, Francesca ALGIERI
  • Publication number: 20200353021
    Abstract: The present invention refers to a composition including a fermented supernatant of Lactobacillus casei or paracasei species The species is characterized by having in its DNA genome at least one DNA sequence essentially identical to one of the sequences selected from the group consisting of: SEQ ID No 1 to 5, and proper diluents and/or carriers and/or excipients. The compositions can be used in the treatment and/or prevention of skin and/or dermatological diseases related to inflammation, allergic reactions, contact hypersensitivity reactions and intolerance, excessive sebaceous secretion, exfoliation or microbial dysbiosis, preferably of the epidermis.
    Type: Application
    Filed: February 4, 2019
    Publication date: November 12, 2020
    Applicant: POSTBIOTICA S.R.L.
    Inventors: Maria RESCIGNO, Giuseppe PENNA, Francesca ALGIERI
  • Publication number: 20190175670
    Abstract: The invention refers to a composition comprising a fermented product of Lactobacillus casei or paracasei species, preferably for use in the treatment of eye inflammation syndromes and to a method for obtaining the same.
    Type: Application
    Filed: August 3, 2017
    Publication date: June 13, 2019
    Applicant: ISTITUTO EUROPEO DI ONCOLOGIA S.R.L.
    Inventors: Maria RESCIGNO, Giuseppe PENNA
  • Publication number: 20180346513
    Abstract: The present invention refers to a method for obtaining a cell culture supernatant or a fraction thereof having a specific tumor antigen peptide repertoire having the steps of: a) exposing in suitable conditions a tumor cell culture expressing the specific tumor antigen peptide repertoire to a Pattern Recognition Receptor (PRR) agonist and/or to one inflammatory cytokine to increase the opening of connexin-hemichannels (CxH); b) collecting the cell culture supernatant; and c) optionally obtaining a fraction of the supernatant, wherein the supernatant has MHC class I and MHC class II peptides and non-classical MHC molecules (HLA-E).
    Type: Application
    Filed: November 11, 2016
    Publication date: December 6, 2018
    Inventors: Giuseppe PENNA, Maria RESCIGNO
  • Publication number: 20160052985
    Abstract: The present invention relates to a compound selected in the group consisting of: a) a polypeptide consisting of the C-terminus amino acid sequence of the human Thymic stromal lymphopoietin (TSLP) long isoform (SEQ ID NO: 2), derivatives and fragments thereof; b) a polynucleotide coding for said polypeptide; d) a vector comprising said polynucleotide; c) a host cell genetically engineered expressing said polypeptide, or d) a TSLP long isoform (SEQ ID NO:2) antagonist for use in the treatment or/and prevention and/or diagnosis and/or monitoring of a disorder or pathology characterized by an inflammatory response.
    Type: Application
    Filed: April 4, 2014
    Publication date: February 25, 2016
    Inventors: Maria RESCIGNO, Giuseppe PENNA, Katerina TSILINGIRI, Giulia FORNASA
  • Publication number: 20100069339
    Abstract: There is provided a method of treatment of male sub-fertility by using a vitamin D compound. Compositions and uses are also provided.
    Type: Application
    Filed: October 12, 2007
    Publication date: March 18, 2010
    Applicant: BIOXELL S.P.A.
    Inventors: Luciano Adorini, Giuseppe Penna, Enrico Colli
  • Publication number: 20080293647
    Abstract: There is provided according to the invention a method of treating a patient with bladder cancer by administering a effective amount of a vitamin D compound in combination with one or more other antiproliferative agents. Also provided are uses of a vitamin D compound in combination with one or more other antiproliferative agents and compositions for use in the method.
    Type: Application
    Filed: November 11, 2005
    Publication date: November 27, 2008
    Inventors: Luciano Adorini, Giuseppe Penna
  • Publication number: 20080280859
    Abstract: The invention provides Gemini vitamin D3 compounds, methods for using the compounds to treat vitamin D3 associated states and pharmaceutical compositions containing the compounds.
    Type: Application
    Filed: October 19, 2005
    Publication date: November 13, 2008
    Applicant: BioXell S.p.A.
    Inventors: Luciano Adorini, Giuseppe Penna, Milan R. Uskokovic, Hubert Maehr
  • Publication number: 20080064668
    Abstract: The invention provides (1,3)di-acylated vitamin D3 analogs of cholecalciferol, substituted at carbon (20) with methyl or cyclopropyl wherein carbon (16) is a single or double bond, and carbon (23) is a single, double, or triple bond. Various alkyl or haloalkyl substitutions are incorporated at carbon (25). The invention provides pharmaceutically acceptable esters, salts, and pro-drugs thereof. Methods for using the compounds to treat vitamin D3 associated states, and pharmaceutical compositions containing the compounds are also disclosed.
    Type: Application
    Filed: September 24, 2004
    Publication date: March 13, 2008
    Applicant: BioXell S.p.A.
    Inventors: Milan R. Uskokovic, Luciano Adorini, Giuseppe Penna, Enrico Colli
  • Publication number: 20070032461
    Abstract: The invention provides 1,3 acylated, 24-keto vitamin D3 compounds of formula I: wherein: X1 and X1 are each independently H2 or ?CH2, provided X1 and X1 are not both ?CH2; R1 and R2 are each independently, hydroxyl, OC(O)C1-C4 alkyl, OC(O)hydroxyalkyl, OC(O)haloalkyl, provided that R1 and R2 are not both hydroxyl; R3 and R4 are each independently hydrogen, C1-C4 alkyl, hydroxyalkyl, or haloalkyl, or R3 and R4 taken together with C20 form C3-C6 cylcoalkyl; and R5 and R6 are each independently C1-C4 alkyl, hydroxyalkyl, or haloalkyl; and pharmaceutically acceptable esters, salts, and prodrugs thereof. Methods for using the compounds to treat vitamin D3 associated states, and phar,aceutical compositions containing the compounds are also disclosed.
    Type: Application
    Filed: April 30, 2004
    Publication date: February 8, 2007
    Applicant: BioXell S.p.A.
    Inventors: Luciano Adorini, Giuseppe Penna, Milan Uskokovic, Hubert Maehr