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FUJISAWA PHARMACEUTICAL CO

Overview
  • Total Patents
    10,227
About

FUJISAWA PHARMACEUTICAL CO has a total of 10,227 patent applications. Its first patent ever was published in 1959. It filed its patents most often in Japan, United States and United Kingdom. Its main competitors in its focus markets pharmaceuticals, organic fine chemistry and biotechnology are DU PONT PHARM CO, BISACCHI GREGORY S and AUTIFONY THERAPEUTICS LTD.

Patent filings per year

Chart showing FUJISAWA PHARMACEUTICAL COs patent filings per year from 1900 to 2020

Top inventors

# Name Total Patents
#1 Takasugi Hisashi 754
#2 Oku Teruo 571
#3 Takaya Takao 534
#4 Hashimoto Masashi 494
#5 Tanaka Hirokazu 421
#6 Ueda Ikuo 386
#7 Sakane Kazuo 384
#8 Kamiya Takashi 367
#9 Matsuo Masaaki 341
#10 Teraji Tsutomu 318

Latest patents

Publication Filing date Title
CN1909905A Method for treating erectile dysfunction
IL165449D0 Aminoalcohol derivatives and pharmaceutical compositions containing the same
US2005245540A1 New methods
TW200528440A 2-cyanopyrrolidinecarboxamide compound
WO2005038443A1 Different-kind-of-object detector employing plane spectrometer
JP2005120083A Antitumor agent
US2006063794A1 Method of attenuating graft rejection
US2005025769A1 Method of suppressing ongoing acute allograft rejection
JP2005089450A Prophylactic or therapeutic agent for infectious disease caused by rs virus
WO2005003111A1 Preventive or remedy for viral conjunctivitis
JP2004285075A Method for improving elution property of hardly dispersible medicine
JP2004352712A Agent for preventing or treating influenza
US2005233330A1 Method for identifying myelodysplastic syndrome-specific genes
JP2005295948A Method for identifying myelodysplastic syndrome-specific gene
WO2004093910A1 REMEDY FOR CEREBRAL NEURODEGENERATIVE DISEASES USING PPARδ AGONIST
JP2005297321A Document file
WO2004096289A1 Gene introduction efficiency enhancer
WO2004089939A1 Condensed furan derivatives as adenosine antagonists
GB0402269D0 Method of screening for new drugs
CN1761655A Thiazole derivatives and their use as VAP-1 inhibitors