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OpenTrials
Active, Not Recruiting

NCT Number: NCT03375242

Safety and Efficacy of Xalkori ROS1

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Crizotinib

Drug

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

Primary outcomes

  1. The incidence of adverse drug reactions in this surveillance.

    Time frame: 52 weeks

Secondary outcomes

  1. Objective Response Rate (ORR)

    Time frame: 12, 24, 52 weeks

Sponsors and collaborators

Lead sponsor

Pfizer

Industry

Registry information

Official study title

XALKORI ROS1+NSCLC DRUG USE INVESTIGATION

Important dates

Study start
2017
Primary completion
2026
Study completion
2026
First posted
Dec 18, 2017
Registry last updated
Mar 30, 2026

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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