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Safety and Efficacy of Xalkori ROS1
NOT_RECRUITINGSponsored by Pfizer
No longer actively recruiting
SponsorPfizer
Started2017-10-25
Est. completion2027-03-26
Eligibility
Age18 Years+
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT03375242
Summary
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
Age: 18 Years+Healthy volunteers accepted
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
Conditions3
CancerLung CancerNon Small Cell Lung Cancer
Interventions1
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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
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No longer actively recruiting
SponsorPfizer
Started2017-10-25
Est. completion2027-03-26
Eligibility
Age18 Years+
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT03375242