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Clinical Trial Summary

This study is designed to evaluate the safety and efficacy of ifinatamab deruxtecan (I-DXd) in combination with immune checkpoint inhibitor (ICI) atezolizumab with or without carboplatin in participants with extensive stage-small cell lung cancer (ES-SCLC) in the first-line (1L) setting.


Clinical Trial Description

This study consists of two parts and two cohorts: Part A (Phase 1b; Safety Run-in) and Part B (Phase 2; Dose Optimization), Cohort 1 (I-DXd in maintenance) and Cohort 2 (I-DXd in induction + maintenance). The primary objective of this study is to evaluate the safety and tolerability of I-DXd in combination with atezolizumab with or without carboplatin by assessing treatment-emergent adverse events (TEAEs) and other safety parameters which will inform optimal dose selection of I-DXd in the combination regimens (Dose Optimization Part B) of this study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06362252
Study type Interventional
Source Daiichi Sankyo
Contact (US) Daiichi Sankyo Contact for Clinical Trial Information
Phone 9089926400
Email CTRinfo@dsi.com
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date June 17, 2024
Completion date December 30, 2026