Pfizer
Tokyo, Japan
NCT Number: NCT03375242
The objective of this surveillance is to collect information about 1) adverse drug reaction not expected from the LPD (unknown adverse drug reaction), 2) the incidence of adverse drug reactions in this surveillance, and 3)factors considered to affect the safety and/or efficacy of this drug.
This study is active but is not currently recruiting participants.
Notify Me18 year and older
All sexes
Observational
Tokyo, Japan
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
XALKORI® Capsule 200 mg/XALKORI® Capsule 250 mg Frequency and duration are according to Package Insert as follows. " The recommended dose schedule of crizotinib is 250 mg taken orally twice daily. Dosing interruption and/or dose reduction may be required based on patients' clinical status. "
Other names: XALKORI® Capsule 200 mg/XALKORI® Capsule 250 mg
Time frame: 52 weeks
Time frame: 12, 24, 52 weeks
Pfizer
Industry
XALKORI ROS1+NSCLC DRUG USE INVESTIGATION
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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