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Restrict the search for
crizotinib
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There is one exact (name or code) match for crizotinib
Status:
US Approved Rx
(2023)
Source:
NDA217581
(2023)
Source URL:
First approved in 2011
Source:
NDA202570
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Conditions:
Crizotinib (trade name Xalkori, Pfizer, Inc.) is an anti cancer drug approved for the treatment of patients with metastatic non-small cell lung cancer (NSCLC) whose tumors are anaplastic lymphoma kinase (ALK)-positive as detected by an FDA-approved test. Crizotinib is an inhibitor of receptor tyrosine kinases including ALK, Hepatocyte Growth Factor Receptor (HGFR, c-Met), ROS1 (c-ros), and Recepteur d’Origine Nantais (RON). Common adverse reactions in clinical trials with crizotinib, occurring at an incidence of 25% or higher, included visual disorders, nausea, diarrhea, vomiting, constipation, edema, elevated transaminases, and fatigue. Crizotinib is currently under investigational study for use in treatment of Uveal Melanoma.
Status:
US Approved Rx
(2023)
Source:
NDA217581
(2023)
Source URL:
First approved in 2011
Source:
NDA202570
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Conditions:
Crizotinib (trade name Xalkori, Pfizer, Inc.) is an anti cancer drug approved for the treatment of patients with metastatic non-small cell lung cancer (NSCLC) whose tumors are anaplastic lymphoma kinase (ALK)-positive as detected by an FDA-approved test. Crizotinib is an inhibitor of receptor tyrosine kinases including ALK, Hepatocyte Growth Factor Receptor (HGFR, c-Met), ROS1 (c-ros), and Recepteur d’Origine Nantais (RON). Common adverse reactions in clinical trials with crizotinib, occurring at an incidence of 25% or higher, included visual disorders, nausea, diarrhea, vomiting, constipation, edema, elevated transaminases, and fatigue. Crizotinib is currently under investigational study for use in treatment of Uveal Melanoma.
Status:
Other
Class (Stereo):
CHEMICAL (ABSOLUTE)
Conditions:
(S)-crizotinib was discovered as an attractive chemical entity for further pre-clinical evaluation, and small-molecule inhibitors of MTH1 as a promising novel class of anticancer agents.
Status:
US Approved Rx
(2013)
First approved in 1958
Class:
MIXTURE