CI

At a glance

ClinicalIndex Comparison Record
Phase 2Recruiting· 45 target
Drug / intervention
Etoposide +4 moredrug
Likely dose
Etoposide 100 mgfrom record
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Search/NCT06217757
NCT06217757Phase 2RecruitingOn Track

Phase I Study of Low-Dose Radiotherapy Plus Chemotherapy and Sugemalimab and Olaparib for First-Line Treatment of SLFN-11 Positive Extensive Stage Small Cell Lung Cancer

Sichuan University·interventional·Posted Jan 22, 2024·Updated May 5, 2026

In Brief

A Phase 2 clinical trial evaluating Low-dose radiotherapy, Etoposide, and 3 other interventions for Lung Cancer and Extensive-stage Small-cell Lung Cancer. Currently recruiting, targeting 45 participants across 1 site.

Detailed Summary

The purpose of this study was to evaluate the safety and efficacy of low-dose radiotherapy (LDRT) combined with sugemalimab, olaparib, chemotherapy in the first-line treatment of SLFN-11 positive extensive stage small cell lung cancer.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 2Recruiting
20242025202620272028
First PostedJan 22, 2024
Enrollment StartApr 18, 2024
Primary CompletionOct 31, 2027
Study CompletionOct 31, 2028
TodayJul 1, 2026
Enrollment to primary: 3.5 yearsPosted 2.4 years agoPrimary completion in 1.3 years

Interventions

Low-dose radiotherapyradiation

The LDRT deals with primary tumour in a 15 Gy of 5fractions over five days, starting from Day 1 in the first cycle.

Etoposidedrug

Etoposide will be administered intravenously at a dose of 100 mg/m\^2 on Days 1, 2 and 3 of each 21-day cycle during the induction phase (Cycles 1-4).

Cisplatindrug

Cisplatin will be administered as intravenous infusion at a dose of 25 mg/m\^2 on Days 1, 2 and 3 of each 21-day cycle during the induction phase (Cycles 1-4).

Sugemalimabdrug

Sugemalimab will be administered by intravenous infusion at a dose of 1200mg on Day 1 of each 21-day cycle for a maximum of 2 years or progressive disease or intolerable toxicity.

Olaparibdrug

Olaparib will be administered orally at a dose of 150mg qod Day 1,3,5,7 or 150 mg qd/150 mg bid/300mg in the morning and 150mg in the evening/300 mg bid on Day 1-7 of each 21-day cycle for a maximum of 2 years or progressive disease or intolerable toxicity.