Clinical trial · Interventional
Fruquintinib Combined With Sintilimab and Chemotherapy in the Treatment of Non-Small Cell Lung Cancer
A Single Arm,Open-label, Study of Fruquintinib Combined With Sintilimab and Chemotherapy in Patients With Unresectable or Metastatic Advanced Wild-type Genotype Non-squamous Non-small Cell Lung Cancer
NCT04956146CI-TRIAL-00056810unknownPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
A phase II study to assess the efficacy and safety of Fruquintinib Combined With Sintilimab and Chemotherapy as a first-line treatment in patients with unresectable or metastatic advanced Wild-type Genotype non-squamous Non-small Cell Lung Cancer.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Carcinoma, Non-Small-Cell Lung | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Fruquintinib,Sintilimab,Pemetrexed,Carboplatin | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Fruquintinib Combined With Sintilimab and Chemotherapy
- interventionNames
- Drug: Fruquintinib,Sintilimab,Pemetrexed,Carboplatin
Primary outcomes (1)
- measure
- Progression Free Survival (PFS)
- timeFrame
- up to 24 months
- description
- To assess the efficacy of Fruquintinib Combined With Chemotherapy as second-
Secondary outcomes (3)
- measure
- Objective response rate (ORR)
- timeFrame
- up to 24 months
- description
- CR + PR rate according to the RECIST version 1.1 guidelines.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. Voluntary provision of informed consent. 2. Males or females aged 18-75. 3. Histological or cytologically confirmed NSCLC, metastatic or non-resectable (stage IIIB-Ⅳ). 4. Not suitable for targeted therapy (patients with non-squamous NSCLC have no EGFR, ALK, gene mutation) 5. At least one lesion can be measured by imaging. 6. Have not received systemic treatment in the past. 7. Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0-1. 8. Life expectancy ≥ 12 weeks. 9. Female of childbearing age must have a negative pregnancy test (serum or urine) within 7 days before enrolment. Exclusion Criteria: 1. Histological or cytologically confirmed small cell lung cancer (SCLC), including lung cancer mixed with SCLC and NSCLC. 2. Diagnosed with other malignant diseases other than NSCLC within 5 years. 3. Have participated in other interventional clinical research treatments now or within 4 weeks. 4. Have previously received multi-targeted kinase inhibitors therapy. 5. Have active autoimmune diseases requiring systemic treatment within 2 years. 6. Received systemic glucocorticoid therapy or immunosuppressive therapy within 2 weeks. 7. Clinically uncontrollable pleural effusion/abdominal effusion. 8. Vaccinated vaccines or attenuated vaccines within 4 weeks before the group; 9. Pregnant or breastfeeding females. 10. Other serious hazards to the safety of patients.
References
Publications (0)
Data not yet available
No reference posted for this study.