FOCHON PHARMACEUTICALS LTD has a total of 35 patent applications. It decreased the IP activity by 33.0%. Its first patent ever was published in 2016. It filed its patents most often in WIPO (World Intellectual Property Organization), Australia and Brazil. Its main competitors in its focus markets pharmaceuticals and organic fine chemistry are ENYO PHARMA, BEIJING HANMEI PHARMACEUTICAL CO LTD and SUZHOU KINTOR PHARMACEUTICALS INC.
# | Country | Total Patents | |
---|---|---|---|
#1 | WIPO (World Intellectual Property Organization) | 9 | |
#2 | Australia | 6 | |
#3 | Brazil | 5 | |
#4 | Canada | 3 | |
#5 | EPO (European Patent Office) | 3 | |
#6 | Taiwan | 3 | |
#7 | China | 2 | |
#8 | Republic of Korea | 2 | |
#9 | United States | 2 |
# | Industry | |
---|---|---|
#1 | Pharmaceuticals | |
#2 | Organic fine chemistry |
# | Technology | |
---|---|---|
#1 | Heterocyclic compounds | |
#2 | Therapeutic chemical compounds | |
#3 | Medical preparations |
# | Name | Total Patents |
---|---|---|
#1 | Lin Shu | 27 |
#2 | Wang Weibo | 27 |
#3 | Zhao Xingdong | 27 |
#4 | Tan Rui | 20 |
#5 | Gao Yuwei | 17 |
#6 | Tan Haohan | 17 |
#7 | Liu Qihong | 16 |
#8 | He Chengxi | 16 |
#9 | Liu Hongbin | 16 |
#10 | Zhang Weipeng | 16 |
Publication | Filing date | Title |
---|---|---|
WO2021047584A1 | SUBSTITUTED (2-AZABICYCLO [3.1.0] HEXAN-2-YL) PYRAZOLO [1, 5-a] PYRIMIDINE AND IMIDAZO [1, 2-b] PYRIDAZINE COMPOUNDS AS TRK KINASES INHIBITORS | |
WO2020253659A1 | Heterocyclic derivatives and use thereof | |
WO2020239124A1 | SUBSTITUTED PYRROLO [2, 3-b] PYRIDINE AND PYRAZOLO [3, 4-b] PYRIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS | |
WO2020063860A1 | Naphthyridinone and pyridopyrimidinone compounds useful as kinases inhibitors | |
TW202028209A | Substituted imidazo[1,2-a]pyridine and [1,2,4]triazolo[1,5-a]pyridine compounds as ret kinase inhibitors | |
WO2020063659A1 | Substituted [1, 2, 4] triazolo [1, 5-a] pyridine compounds as ret kinase inhibitors | |
EP3774812A1 | Macrocyclic compounds as trk kinases inhibitors | |
AU2019236892A1 | Deuterated compounds as ROCK inhibitors | |
KR20200141035A | Substituted (2-azabicyclo [3.1.0] hexan-2-yl) pyrazolo [1, 5-a] pyrimidine and imidazo [1, 2-b] pyridazine compounds as TRK kinase inhibitors |