drugset / Trial / NCT02300298

Nintedanib Plus Docetaxel in Japanese Patients With Adenocarcinoma Subtype Non-small Cell Lung Cancer After Failure of First Line Chemotherapy

NCT02300298

Phase 1 Completed 10 enrolled Boehringer Ingelheim
NaSingle-groupOpen-labelTreatment

Summary

To determine the appropriateness of the dose of nintedanib 200 mg b.i.d. plus docetaxel 75 mg/m2 as starting dose by evaluating the safety in Japanese patients with body surface area (BSA) \<1.5 m2 and locally advanced or metastatic adenocarcinoma subtype non-small cell lung cancer (NSCLC) after failure of first line platinum- based chemotherapy

Timeline

Start
2014-12-24
Primary completion
2016-01-15
Completion
2017-10-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Nintedanib Small molecule 200 mg Oral
Background Docetaxel Small molecule 75 mg/m2