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Clinical Trial Summary

This is an open-label, multicenter, single-arm, expanded access study designed to provide alectinib to participants with ALK-rearranged NSCLC after disease progression on or intolerance to prior ALK tyrosine kinase inhibitor (TKI) therapy. Participants will receive alectinib until disease progression, unacceptable toxicity, withdrawal of consent, patient or physician decision to discontinue treatment, death, alectinib becomes commercially available in the United States following approval of alectinib by the FDA, or the Sponsor decides to close the trial, whichever occurs first (approximately 15 months).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02271139
Study type Expanded Access
Source Genentech, Inc.
Contact
Status No longer available
Phase N/A

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