Long Term Safety Observation of Crizotinib in Chinese NSCLC Population

NCT03672643 · Status: TERMINATED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 41

Last updated 2024-11-08

Study results available
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Summary

This study is to allow access to crizotinib who were treated in previous Pfizer-sponsored studies in China.

Conditions

  • ALK or ROS1-positive NSCLC

Interventions

DRUG

Crizotinib

receive crizotinib orally

Sponsors & Collaborators

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-28
Primary Completion
2023-09-28
Completion
2023-09-28

Countries

  • China

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03672643 on ClinicalTrials.gov