drugset / Trial / NCT05815160

Debio 0123 in Combination With Carboplatin and Etoposide in Adult Participants With Small Cell Lung Cancer That Recurred or Progressed After Previous Standard Platinum-Based Therapy

NCT05815160

Phase 1 Terminated 34 enrolled Debiopharm International SA
Non-randomizedSequentialOpen-labelTreatment

Summary

The primary purpose of part 1 (dose escalation) of this study is to identify the recommended dose and to characterize the safety and tolerability of Debio 0123 in combination with carboplatin and etoposide. The primary purpose of part 2 (dose expansion) of this study is to characterize the safety and tolerability of Debio 0123 at the recommended dose when administered in combination with carboplatin and etoposide.

Timeline

Start
2023-05-02
Primary completion
2026-03-09
Completion
2026-03-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Debio 0123 Unknown Oral
Background Carboplatin Small molecule Intravenous
Background Etoposide Small molecule Intravenous