PEMAZYRE®▼ (pemigatinib)
PEMAZYRE monotherapy is indicated for the treatment of adults with locally advanced or metastatic cholangiocarcinoma with a
fibroblast growth factor receptor 2 (FGFR2) fusion or rearrangement that have progressed after at least one prior line of systemic therapy1*
self–directed learning material works
- PEMAZYRE® (pemigatinib). Summary of Product Characteristics. Section 4.1. June 2022.
*This medicinal product has been authorised under a ‘conditional approval’ scheme. This means that further evidence on this medicinal product is awaited. The EMA will review new information on this medicinal product at least every year and the SmPC will be updated as necessary.1
NO/PEMA/P/22/0013
Date of preparation: June 2022
© 2022, Incyte. All rights reserved.
PEMAZYRE, the PEMAZYRE logo and the Incyte logo are registered trademarks of Incyte.
NO/PEMA/P/22/0013
Date of preparation: June 2022
© 2022, Incyte. All rights reserved.
PEMAZYRE, the PEMAZYRE logo and the Incyte logo are registered trademarks of Incyte.
▼ This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions. For further information, please refer to the Summary of Product Characteristics.1
Prescribing information can be accessed via the 'API' icon in the navigation panel at the bottom of each screen.
Prescribing information can be accessed via the 'API' icon in the navigation panel at the bottom of each screen.
Abbreviations
1L
first-line
2L
second-line
ABC
advanced biliary tract cancer
API
abridged product information
AR
adverse reaction
ASC
active symptom control
BRAF
v-raf murine sarcoma viral oncogene homolog B1
BTC
biliary tract cancer
CCA
cholangiocarcinoma
CI
confidence interval
CNS
central nervous system
CR
complete response
CYP2B6
cytochrome P450 2B6
CYP3A4
cytochrome P450 3A4
dCCA
distal cholangiocarcinoma
DOR
duration of response
eCCA
extrahepatic cholangiocarcinoma
ECOG
Eastern Cooperative Oncology Group
EGFR
epidermal growth factor receptor
EMA
European Medicines Agency
ESMO
European Society for Medical Oncology
EU
European Union
FGFR
fibroblast growth factor receptor
FOLFOX
folinic acid, fluorouracil and oxaliplatin
HR
hazard ratio
iCCA
intrahepatic cholangiocarcinoma
IDH
isocitrate dehydrogenase
KM
Kaplan-Meier
KRAS
Kirsten rat sarcoma viral oncogene homolog
MATE1
multidrug and toxin extrusion protein 1
MDT
multidisciplinary team
mg
milligram
mg/dL
milligram per decilitre
MSI-H
microsatellite instability-high
NGS
next-generation sequencing
NTRK
neurotrophic tyrosine receptor kinase
OCT
optical coherence tomography
OCT2
organic cation transporter-2
ORR
overall response rate
OS
overall survival
pCCA
perihilar cholangiocarcinoma
P-gp
P-glycoprotein
PPES
palmar-plantar erythrodysaesthesia syndrome
PR
partial response
PS
performance status
RECIST
Response Evaluation Criteria in Solid Tumours
SmPC
Summary of Product Characteristics
SOC
standard of care
Norway API
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