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SEATTLE CHILDRENS HOSPITAL DBA SEATTLE CHILDRENS RES INST

Overview
  • Total Patents
    189
  • GoodIP Patent Rank
    7,912
  • Filing trend
    ⇧ 57.0%
About

SEATTLE CHILDRENS HOSPITAL DBA SEATTLE CHILDRENS RES INST has a total of 189 patent applications. It increased the IP activity by 57.0%. Its first patent ever was published in 2009. It filed its patents most often in EPO (European Patent Office), Australia and WIPO (World Intellectual Property Organization). Its main competitors in its focus markets biotechnology, pharmaceuticals and foods and drinks are TIANJIN HENGJIA BIOTECHNOLOGY DEV CO LTD, PRECIGEN INC and PETRIK JURAJ.

Patent filings per year

Chart showing SEATTLE CHILDRENS HOSPITAL DBA SEATTLE CHILDRENS RES INSTs patent filings per year from 1900 to 2020

Top inventors

# Name Total Patents
#1 Jensen Michael C 86
#2 Rawlings David J 51
#3 Scharenberg Andrew M 43
#4 Sommer Karen 28
#5 Honaker Yuchi Chiang 23
#6 Khan Iram F 18
#7 Johnson Adam 17
#8 Tampella Giacomo 16
#9 Torgerson Troy 14
#10 Matthaei James 13

Latest patents

Publication Filing date Title
WO2020264039A1 Artificial antigen-specific immunoregulatory t (airt) cells
WO2020219425A1 Combinatorial car t cell and hematopoeitic stem cell genetic engineering for specific immunotherapy of myeloid leukemias
WO2020190925A1 Methods and compositions for engineering cd4-deficient car t cells and anti-cd4 car t cells and uses thereof
WO2020185917A1 Sodium fluorescein as a reversal agent for an anti-fluorescein car t cells and fluorescein-phospholipid-ethers or profluorescein-phospholipid-ethers
AU2019333149A1 Methods and compositions comprising B7H3 chimeric antigen receptors
WO2020047165A1 Self-inactivating transposase plasmids and uses thereof
AU2019319674A1 Methods and compositions for stimulation of chimeric antigen receptor T cells with hapten labelled cells
WO2019210057A1 Rapamycin resistant cells
CA3091688A1 Expression of foxp3 in edited cd34+ cells
AU2019257708A1 Expression of human FOXP3 in gene edited T cells
CA3106812A1 Homology-directed repair template design and delivery to edit hemoglobin-related mutations
CA3098489A1 Therapeutic genome editing in x-linked hyper igm syndrome
EP3765041A1 Il-13 receptor alpha 2 (il13ra2) chimeric antigen receptor for tumor specific t cell immunotherapy
AU2019234580A1 IL-13 receptor alpha 2 targeted, zetakine directed T cell immunotherapy
EP3749695A1 Fluorescein-specific cars exhibiting optimal t cell function against fl-ple labelled tumors
WO2019038660A1 Exosome profiling for diagnosis and monitoring of vasculitis and vasculopathies including kawasaki disease
AU2018270156A1 Generating mammalian T cell activation inducible synthetic promoters (syn+pro) to improve T cell therapy
WO2018200597A1 Homology directed repair compositions for the treatment of hemoglobinopathies
CA3060570A1 Therapeutic genome editing in wiskott-aldrich syndrome and x-linked thrombocytopenia
AU2018256412A1 Optimized lentiviral vector for XLA gene therapy