CI

At a glance

ClinicalIndex Comparison Record
Phase 2Recruiting· 47 target
Drug / intervention
Chemotherapy +5 moredrug
Likely dose
Angio-immuno kinase inhibitor 200 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06719700
NCT06719700Phase 2RecruitingOn TrackUpdated 3mo ago

A Prospective Phase II Study of Concurrent Chemoradiotherapy Combined With Toripalimab and Surufatinib in the Treatment of Limited-Stage Small Cell Lung Cancer

Sun Yat-sen University·interventional·Posted Dec 6, 2024·Updated Mar 3, 2026

In Brief

A Phase 2 clinical trial evaluating Chemotherapy, Immunotherapy, and 4 other interventions for Toripalimab and 3 related conditions. Currently recruiting, targeting 47 participants across 1 site.

Detailed Summary

Based on the preclinical rationale for combining surufatinib with immunotherapy, and the clinical efficacy observed with surufatinib in extensive-stage small cell lung cancer (ES-SCLC), the investigators hypothesize that incorporating surufatinib into the ADRIATIC regimen could further enhance survival in LS-SCLC. To evaluate this approach, the investigators plan to conduct a single-arm Phase II study to explore the safety and efficacy of concurrent chemoradiotherapy combined with toripalimab and surufatinib in treating LS-SCLC.

Study Details

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

Timeline

Phase 2Recruiting
20252026202720282029
First PostedDec 6, 2024
Enrollment StartNov 30, 2024
Primary CompletionNov 29, 2028
TodayJul 1, 2026
Enrollment to primary: 4.0 yearsPosted 1.6 years agoPrimary completion in 2.4 years

Interventions

Chemotherapydrug

Etoposide combined with cisplatin or carboplatin, administered every three weeks for a total of four cycles.

Immunotherapydrug

Toripalimab was administered concurrently with chemotherapy, every three weeks for four cycles.

Angio-immuno kinase inhibitordrug

Oral surufatinib 200 mg once daily (q.d.), given on days 1-14 of each chemotherapy cycle.

radiotherapyradiation

Thoracic radiotherapy will begin no later than the start of the third chemotherapy cycle.

Prophylactic Cranial Irradiationradiation

PCI is recommended after the completion of chemoradiotherapy.

Consolidation Therapy with Toripalimab and Surufatinibdrug

Patients achieving complete response (CR), partial response (PR), or stable disease (SD) following chemoradiotherapy will receive consolidation therapy. Toripalimab: 240 mg intravenously on day 1, every three weeks. Surufatinib: 200 mg orally on days 1-14, every three weeks.