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Safety and Efficacy of Xalkori ROS1
Safety and Efficacy of Xalkori ROS1

NCT03375242

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