Crizotinib Expanded Access Protocol For ROS1 Positive NSCLC

NCT02824094 · Status: NO_LONGER_AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2017-07-21

No results posted yet for this study

Summary

Primary objective of this study is to allow access and evaluate the safety of crizotinib for patients in Japan with advanced NSCLC harboring a translocation or inversion involving the ROS1 oncogene.

Conditions

  • Neoplasms
  • Carcinoma, Non-Small-Cell Lung

Interventions

DRUG

crizotinib

Crizotinib, 250 mg BID, will be administered orally on a continuous daily dosing schedule

Sponsors & Collaborators

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Countries

  • Japan

Study Locations

More Related Trials

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 NCT02824094 on ClinicalTrials.gov