Clinical trial information
Select trial for more information
Targeted inhibition of tumors harboring activating mutations in epidermal growth factor receptor (EGFR) has helped to advance the treatment approach for advanced non-small cell lung carcinoma (NSCLC).
While the majority of these activating mutations also sensitize EGFR (EGFRm) to effective targeting by early-generation EGFR-tyrosine kinase inhibitors (TKIs), the emergence of a secondary resistance mutation (EGFR T790M) results in treatment-refractory NSCLC disease progression. Approximately 51%-68% of tumors that progress on a first- and second-generation EGFR TKI are EGFR T790M mutation positive.1-7
Osimertinib is a third-generation, irreversible, CNS-active EGFR-TKI designed to selectively target both EGFR-sensitizing (ie, T790M, L858R and exon 19 deletion) and EGFR T790M-resistance mutations.1,8
Osimertinib is being clinically evaluated in EGFRm-containing NSCLC.
Select trial for more information
first line
second line
antibody drug conjugate
adverse event
area under the curve
blinded independent central review
central nervous system
complete pathological response
colorectal cancer
chemoradiotherapy
chemotherapy
Common Terminology Criteria for Adverse Events
circulating tumor DNA
disease control rate
disease-free survival
duration of response
electrocardiogram
Eastern Cooperative Oncology Group Performance Score
event-free survival
epidermal growth factor receptor
epidermal growth factor receptor mutation
epidermal growth factor receptor wild type
European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire
exon 19 deletion
fluorescence in situ hybridization
fluorescence in situ hybridization (MET copy ≥10)
gray
hepatitis B virus
hepatitis C virus
human immunodeficiency virus
head and neck squamous cell carcinoma
health-related quality of life
International Association For The Study Of Lung Cancer
independent central review
3+ immunohistochemistry overexpression in 90% of tumor cells
interstitial lung disease
intravenous
exon 21 L858R point mutation
hepatocyte growth factor receptor
large cell neuroendocrine carcinoma
non-small cell lung cancer
once daily
overall or objective response rate
overall survival
progressive disease
progression-free survival
time to second progression or death
PFS at 24 months from randomization
pharmacokinetics
per oral
phosphatidylserine
platinum-based chemotherapy
every * weeks
every 3 weeks
once daily
randomization
Response Evaluation Criteria in Solid Tumors
Response Evaluation Criteria in Solid Tumors version 1.1
radiotherapy
stereotactic body radiation therapy
small cell lung cancer
standard of care
time to discontinuation or death
time to first subsequent therapy
tyrosine kinase inhibitor
tumor node metastasis staging
Tumor Node Metastasis 8th edition
transformed small cell lung cancer
time to start of second subsequent therapy
time to treatment discontinuation
time to death or distant metastases
time to progression
World Health Organization
World Health Organization performance status
wild type
Select trial for more information
first line
second line
antibody drug conjugate
adverse event
area under the curve
blinded independent central review
central nervous system
complete pathological response
colorectal cancer
chemoradiotherapy
chemotherapy
Common Terminology Criteria for Adverse Events
circulating tumor DNA
disease control rate
disease-free survival
duration of response
electrocardiogram
Eastern Cooperative Oncology Group Performance Score
event-free survival
epidermal growth factor receptor
epidermal growth factor receptor mutation
epidermal growth factor receptor wild type
European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire
exon 19 deletion
fluorescence in situ hybridization
fluorescence in situ hybridization (MET copy ≥10)
gray
hepatitis B virus
hepatitis C virus
human immunodeficiency virus
head and neck squamous cell carcinoma
health-related quality of life
International Association For The Study Of Lung Cancer
independent central review
3+ immunohistochemistry overexpression in 90% of tumor cells
interstitial lung disease
intravenous
exon 21 L858R point mutation
hepatocyte growth factor receptor
large cell neuroendocrine carcinoma
non-small cell lung cancer
once daily
overall or objective response rate
overall survival
progressive disease
progression-free survival
time to second progression or death
PFS at 24 months from randomization
pharmacokinetics
per oral
phosphatidylserine
platinum-based chemotherapy
every * weeks
every 3 weeks
once daily
randomization
Response Evaluation Criteria in Solid Tumors
Response Evaluation Criteria in Solid Tumors version 1.1
radiotherapy
stereotactic body radiation therapy
small cell lung cancer
standard of care
time to discontinuation or death
time to first subsequent therapy
tyrosine kinase inhibitor
tumor node metastasis staging
Tumor Node Metastasis 8th edition
transformed small cell lung cancer
time to start of second subsequent therapy
time to treatment discontinuation
time to death or distant metastases
time to progression
World Health Organization
World Health Organization performance status
wild type