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Clinical Trial Summary

The primary purpose of part 1 (dose escalation) of this study is to identify the recommended phase 2 dose (RP2D) 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 RP2D when administered in combination with carboplatin and etoposide.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05815160
Study type Interventional
Source Debiopharm International SA
Contact Debiopharm International S.A
Phone +41 21 321 01 11
Email clinicaltrials@debiopharm.com
Status Recruiting
Phase Phase 1
Start date May 2, 2023
Completion date April 2026

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