Pre-treated non-small cell lung cancer
Conditions
Interventions
Oral S-1 with leucovorin
Sponsors
Protocol team for S-1 with leucovorin therapy
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: patients with measurable disease and good performance status
Exclusion criteria
Exclusion criteria: patients with symptomatic brain metastasis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| response rate | — |
Secondary
| Measure | Time frame |
|---|---|
| Safety, overall survival, progression free survival, and 1-year survival | — |
Countries
Japan
Contacts
Public ContactMegumi Isii
Pharma Valley Center Clinical trial center
Outcome results
None listed