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Evaluation of the Efficacy and Safety of Jianpi Bushen Jiedu Formula Combined with Serplulimab Plus Etoposide/Carboplatin in the Treatment of Extensive-Stage Small Cell Lung Cancer

Evaluation of the Efficacy and Safety of Jianpi Bushen Jiedu Formula Combined with Serplulimab Plus Etoposide/Carboplatin in the Treatment of Extensive-Stage Small Cell Lung Cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001799
Enrollment
Unknown
Registered
2025-09-21
Start date
2024-12-01
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Small cell lung cancer

Interventions

Control group:Traditional Chinese medicine placebo + slulizumab combined with etoposide/carboplatin chemotherapy
Experimental group:Traditional Chinese medicine granules combined with slulizumab and etoposide/carboplatin chemotherapy

Sponsors

Longhua Hospital Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Diagnosed with primary bronchogenic carcinoma according to Western medicine criteria and confirmed as small cell lung cancer (SCLC) through cytological or pathological examination; 2.Clinically staged as extensive-stage SCLC ; 3.Traditional Chinese medicine syndrome differentiation indicates spleen and kidney deficiency syndrome; 4.No prior treatment including chemotherapy radiotherapy immunotherapy or targeted therapy; 5.Eastern Cooperative Oncology Group performance status (PS) score =3 with an estimated survival of at least 3 months; 6.Age between 18 and 80 years (inclusive) with no gender restrictions; 7.Hematological criteria: absolute neutrophil count (ANC) >1.5×10^9/L platelet count (PLT) >80×10^9L hemoglobin (Hb) >100 g/L; normal liver and renal function; 8.Good patient compliance with the ability to understand the study and voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Known allergy to any component of this drug; 2.Pregnant or breastfeeding women; 3.Currently participating in other drug trials; 4.Presence of other malignancies or severe comorbidities; patients with immune system disorders such as HIV/AIDS autoimmune hepatitis systemic lupus erythematosus rheumatoid diseases ankylosing spondylitis Sjögrens syndrome etc.; 5.Patients with mental illness who are unable to comply with the study protocol; 6. Currently participating in other clinical drug trials; 7.Refusal to comply with follow-up requirements; 8.Any other reason that the investigator deems the patient unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Progress Free Survival;

Secondary

MeasureTime frame
Indicators of immunity;Overall Survival;Quality of life;Objective Response Rate;1-year survival rate;Disease Control Rate;

Countries

CHINA

Contacts

Public ContactLei ZHOU

Department of Oncology Longhua Hospital Shanghai University of Traditional Chinese Medicine Shanghai China

lucyzhou100@163.com13641759529

Outcome results

None listed

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