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Fulranumab is a monoclonal antibody against nerve growth factor. It was designed for the treatment of pain. Johnson & Johnson licensed the drug from Amgen in a deal valued at around US$425 million in 2008. In 2016 Johnson & Johnson discontinued all phase III trials of fulranumab and returned the rights to its originator. The company said the decision was based on "strategic portfolio prioritisation and was not based on any emerging safety concerns from the phase III clinical studies with fulranumab" in osteoarthritic pain.

AttributesValues
rdf:type
rdfs:label
  • فولرانوماب (ar)
  • Fulranumab (en)
rdfs:comment
  • فولرانوماب هو جسم مضاد وحيد النسيلة بشري مصمم لعلاج الألم، طورته جونسون وجونسون. (ar)
  • Fulranumab is a monoclonal antibody against nerve growth factor. It was designed for the treatment of pain. Johnson & Johnson licensed the drug from Amgen in a deal valued at around US$425 million in 2008. In 2016 Johnson & Johnson discontinued all phase III trials of fulranumab and returned the rights to its originator. The company said the decision was based on "strategic portfolio prioritisation and was not based on any emerging safety concerns from the phase III clinical studies with fulranumab" in osteoarthritic pain. (en)
dcterms:subject
Wikipage page ID
Wikipage revision ID
Link from a Wikipage to another Wikipage
sameAs
dbp:wikiPageUsesTemplate
ATC prefix
  • none (en)
c
CAS number
ChemSpiderID
  • none (en)
H
KEGG
  • D09907 (en)
n
O
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source
  • u (en)
target
type
  • mab (en)
UNII
Verifiedfields
  • changed (en)
verifiedrevid
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  • changed (en)
has abstract
  • فولرانوماب هو جسم مضاد وحيد النسيلة بشري مصمم لعلاج الألم، طورته جونسون وجونسون. (ar)
  • Fulranumab is a monoclonal antibody against nerve growth factor. It was designed for the treatment of pain. Johnson & Johnson licensed the drug from Amgen in a deal valued at around US$425 million in 2008. In 2016 Johnson & Johnson discontinued all phase III trials of fulranumab and returned the rights to its originator. The company said the decision was based on "strategic portfolio prioritisation and was not based on any emerging safety concerns from the phase III clinical studies with fulranumab" in osteoarthritic pain. (en)
mab type
  • mab (en)
gold:hypernym
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page length (characters) of wiki page
CAS number
  • 902141-80-4
FDA UNII code
  • 0E986JU40I
KEGG
  • D09907
foaf:isPrimaryTopicOf
is Link from a Wikipage to another Wikipage of
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