Non-small Cell Lung Cancer Clinical Trial
Official title:
TIGER-2: A Phase 2, Open-label, Multicenter, Safety and Efficacy Study of Oral CO-1686 as 2nd Line EGFR-directed TKI in Patients With Mutant EGFR Non-small Cell Lung Cancer (NSCLC)
The purpose of this study is to evaluate the safety and anti-tumor effect of rociletinib. The trial is open-ended, which means patients will continue to take rociletinib until the study doctor determines it is no longer beneficial for them.
This is a Phase 2, single arm, open-label, dual cohort, multicenter study evaluating the
safety and efficacy of rociletinib administered orally to patients with previously treated
mutant EGFR NSCLC.
Patients will be enrolled into 2 cohorts. Cohort A will enroll approximately 125 eligible
patients who are centrally confirmed T790M-positive. Cohort B will be a continuation of the
study and will enroll up to approximately 100 eligible patients who will be either centrally
confirmed T790M-positive or T790M-negative.
All patients (for Cohort A and B) should have experienced disease progression while on
treatment with the first single-agent EGFR-directed TKI (EGFR-TKI) for advanced/metastatic
NSCLC. One line of chemotherapy prior to the EGFR-TKI treatment is permissible.
The study (Cohorts A and B) will consist of a screening phase to establish study eligibility
and document baseline measurements, an open-label treatment phase, in which the patient will
receive rociletinib to ascertain safety and efficacy until disease progression as defined by
RECIST Version 1.1, clinical tumor progression, or unacceptable toxicity as assessed by the
investigator. For patients with clinical progression, radiographic assessment should be
performed to document evidence of radiographic progression.
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