drugset / Trial / NCT01933932

Assess Efficacy & Safety of Selumetinib in Combination With Docetaxel in Patients Receiving 2nd Line Treatment for v-Ki-ras2 Kirsten Rat Sarcoma Viral Oncogene Homolog (KRAS) Positive NSCLC

NCT01933932

Phase 3 Active not recruiting 510 enrolled AstraZeneca
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess the efficacy of selumetinib in combination with docetaxel (75mg/m2) vs placebo in combination with docetaxel (75mg/m2) in patients with locally advance or metastatic NSCLCs that harbor mutations of KRAS. This study will also assess the PK, safety, patient reported outcomes (PRO) and tolerability profile of the selumetinib/docetaxel combination, compared to placebo in combination with docetaxel

Timeline

Start
2013-09-25
Primary completion
2016-06-07
Completion
2025-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Selumetinib Small molecule 75 mg Oral
Background Docetaxel Small molecule 75 mg/m2 Intravenous
Background Pegfilgrastim Protein / enzyme biologic