Clinical Trials Logo

Clinical Trial 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.


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

See also
  Status Clinical Trial Phase
Completed NCT03823118 - S1 Plus Anlotinib in Treating Patients With Refractory or Relapsed Small-cell Lung Cancer Phase 2
Recruiting NCT03262454 - Sequential Hypofractionated Radiotherapy Followed by Anti-PD-L1 Atezolizumab for SCLC Phase 2
Terminated NCT02477813 - Temozolomide in Patients Affected by Relapsed Sensitive or Refractory Small Cell Lung Cancer With MGMT Methylation Phase 2
Not yet recruiting NCT06258642 - Irinotecan Liposome Combined With Anlotinib as Second-line Regimen for SCLC N/A
Terminated NCT05027867 - KRT-232 in Subjects With Relapsed or Refractory Small Cell Lung Cancer Phase 2
Completed NCT01441297 - BIBF 1120 as Second Line Treatment for Small Cell Lung Cancer Phase 2
Recruiting NCT03994744 - Assessing Safety and Efficacy of Sintilimab and Metformin Combination Therapy in SCLC Phase 2