drugset / Trial / NCT01839032

Oral Vinorelbine as Induction Chemotherapy Followed Concomitant Chemoradiotherapy

NCT01839032 ↗

Phase 2 Completed 70 enrolled Pierre Fabre Laboratories
NaSingle-groupOpen-labelTreatment

Summary

Patients (pts) with stage IIIA/IIIB NSCLC received NVBiv 25 mg/m² + CDDP 80 mg/m² on D1 and NVBo 60 mg/m² on D8 every 3 weeks (q3w) for 2 cycles as induction. Pts with response or non change received NVBo 20 mg fixed dose on D1 D3 D5 + CDDP 80 mg/m² on D1 q3w for 2 more cycles during RT(66 Gy/6.5 w).

Timeline

Start
2005-05
Primary completion
2008-10
Completion
2008-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Cisplatin Other / unclassified 80 mg/m2 Intravenous
Subject Vinorelbine Small molecule 20 mg Intravenous
Subject Vinorelbine Small molecule 25 mg/m2 Intravenous
Subject Vinorelbine Small molecule 60 mg/m2 Intravenous

Indications