drugset / Trial / NCT03098030

Dinutuximab and Irinotecan Versus Irinotecan to Treat Subjects With Relapsed or Refractory Small Cell Lung Cancer

NCT03098030

Phase 2/3 Completed 483 enrolled United Therapeutics
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a 2-part, multicenter, open-label, randomized study of dinutuximab and irinotecan versus irinotecan alone in subjects with relapsed or refractory small cell lung cancer (SCLC). Part 1 of the study involves intrasubject dose escalation to evaluate the safety and tolerability of dinutuximab in combination with irinotecan. Part 2 of the study is designed to determine whether dinutuximab plus irinotecan prolongs overall survival (OS) compared with irinotecan alone. Subjects in Part 2 will be randomized in a 2:2:1 fashion to 1 of 3 treatment groups: (A) irinotecan; (B) dinutuximab plus irinotecan; or (C) topotecan. Randomization will be stratified by duration of response to prior platinum therapy (relapse-free period \<3 months or ≥3 months).

Timeline

Start
2017-06-01
Primary completion
2020-01-27
Completion
2020-03-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Dinutuximab Monoclonal antibody 10 mg/m2 Intravenous
Subject Dinutuximab Monoclonal antibody 16 mg/m2 Intravenous
Subject Dinutuximab Monoclonal antibody 17.5 mg/m2 Intravenous
Subject Irinotecan Small molecule 350 mg/m2 Intravenous
Comparator Topotecan Small molecule 1.5 mg/m2 Intravenous