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Safety and Efficacy of Xalkori ROS1
Safety and Efficacy of Xalkori ROS1
Active Not RecruitingN/A
Sponsor: Pfizer
Conditions: Non-small Cell Lung Cancer
Interventions: crizotinib
Countries: Japan
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.
Eligibility overview
Sex: ALL
Age: 18 Years to —
Healthy volunteers: No
Study type: OBSERVATIONAL
Eligibility criteria
Inclusion Criteria: * patients with unresectable progressive/recurrent NSCLC who are naive to XALKORI and whose tumor is ROS1 gene positive Exclusion Criteria: * Patients with past history of hypersensitivity to any of the ingredients of XALKORI
Locations (1)
- Tokyo, Japan