About: Cemiplimab     Goto   Sponge   NotDistinct   Permalink

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Cemiplimab, sold under the brand name Libtayo, is a monoclonal antibody medication for the treatment of squamous cell skin cancer. Cemiplimab belongs to a class of drugs that binds to the programmed death receptor-1 (PD-1), blocking the PD-1/PD-L1 pathway. The most common side effects include fatigue, rash, diarrhea, musculoskeletal pain, and nausea. Cemiplimab is the first FDA approval of a medication specifically for advanced cutaneous squamous cell carcinoma (CSCC).

AttributesValues
rdf:type
rdfs:label
  • Cemiplimab (en)
  • Cemiplimab (fr)
rdfs:comment
  • Le cemiplimab est un anticorps monoclonal ciblant le PD1 et utilisé dans le traitement de certains cancers. (fr)
  • Cemiplimab, sold under the brand name Libtayo, is a monoclonal antibody medication for the treatment of squamous cell skin cancer. Cemiplimab belongs to a class of drugs that binds to the programmed death receptor-1 (PD-1), blocking the PD-1/PD-L1 pathway. The most common side effects include fatigue, rash, diarrhea, musculoskeletal pain, and nausea. Cemiplimab is the first FDA approval of a medication specifically for advanced cutaneous squamous cell carcinoma (CSCC). (en)
dcterms:subject
Wikipage page ID
Wikipage revision ID
Link from a Wikipage to another Wikipage
Link from a Wikipage to an external page
sameAs
dbp:wikiPageUsesTemplate
ATC suffix
  • FF06 (en)
ATC prefix
  • L01 (en)
c
CAS number
ChemSpiderID
  • none (en)
DrugBank
  • DB14707 (en)
elimination half-life
H
KEGG
  • D11108 (en)
legal status
  • Rx-only (en)
legal US
  • Rx-only (en)
MedlinePlus
  • a618054 (en)
n
O
routes of administration
s
source
  • u (en)
synonyms
  • REGN-2810, REGN2810, cemiplimab-rwlc (en)
target
tradename
  • Libtayo (en)
type
  • mab (en)
UNII
has abstract
  • Cemiplimab, sold under the brand name Libtayo, is a monoclonal antibody medication for the treatment of squamous cell skin cancer. Cemiplimab belongs to a class of drugs that binds to the programmed death receptor-1 (PD-1), blocking the PD-1/PD-L1 pathway. The most common side effects include fatigue, rash, diarrhea, musculoskeletal pain, and nausea. In September 2018, it was approved by the U.S. Food and Drug Administration (FDA) for treating people with metastatic cutaneous squamous cell carcinoma (CSCC) or locally advanced CSCC who are not candidates for curative surgery or curative radiation. It was approved for medical use in the European Union in June 2019. It was approved for medical use in Australia in July 2020. Cemiplimab is the first FDA approval of a medication specifically for advanced cutaneous squamous cell carcinoma (CSCC). (en)
  • Le cemiplimab est un anticorps monoclonal ciblant le PD1 et utilisé dans le traitement de certains cancers. (fr)
DailyMedID
  • Cemiplimab (en)
legal AU
  • S4 (en)
legal CA
  • Rx-only / Schedule D (en)
legal EU
  • Rx-only (en)
mab type
  • mab (en)
pregnancy AU
  • D (en)
pronounce
  • sem' ip li" mab (en)
prov:wasDerivedFrom
page length (characters) of wiki page
alternative name
  • Libtayo (en)
CAS number
  • 1801342-60-8
DrugBank
  • DB14707
FDA UNII code
  • 6QVL057INT
KEGG
  • D11108
MedlinePlus
  • a618054
foaf:isPrimaryTopicOf
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