Skip to content

A multi-center clinical study of a new type of immune combination therapy in advanced lung cancer

A multi-center clinical study of a new type of immune combination therapy in advanced lung cancer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035509
Enrollment
Unknown
Registered
2020-08-13
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

lung cancer

Interventions

A:ETSIC+PD-1 monoantibody
B:Pemetrexed+Carboplatin+ETSIC
C:Pemetrexed + Carboplatin

Sponsors

Shanghai Chest Hospital Affiliated to Shanghai Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Gene editing technology to screen people who benefit from ETSIC treatment; 2. Newly treated stage IV adenocarcinoma; 3. Negative driver gene; 4. PD-L1 expression is positive; 5. Have tumor tissue available for biomarker detection; 6. aged 18-75 years old; 7. PS 0-1 points; 8. Rule out symptomatic brain metastases.

Exclusion criteria

Exclusion criteria: 1) The patient has been treated with immune checkpoint inhibitors such as anti-PD-1, PD-L1 or CTLA-4 therapy; 2) Patients who have received systemic platinum dual-drug chemotherapy as advanced treatment; 3) The patient received other approved systemic anticancer therapy or systemic immunomodulators (including but not limited to interferon, interleukin 2 and tumor necrosis factor) 4 weeks before the first dose; 4) The patient is accompanied by refractory pleural fluid or ascites, such as pleural fluid or ascites that needs to be punctured and drained within 2 weeks before the first administration; 5) Active leptomeningeal disease or brain metastasis, if there are central nervous system symptoms, interventional treatment (including but not limited to radiotherapy, lowering intracranial pressure, etc.) is required.

Design outcomes

Primary

MeasureTime frame
PFS;

Secondary

MeasureTime frame
ORR;DCR;OS;safety;

Countries

China

Contacts

Public ContactHan Baohui

Shanghai Chest Hospital Affiliated to Shanghai Jiaotong University

18930858216@163.com+86 18930858216

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026