Clinical trial · Interventional
Endostar Continued Pumping Into Vein Combining With Gemcitabine-Carboplatin to Treat Non-Small Cell Lung Cancer (NSCLC)
A Randomized, Open Label, Controlled Study About Endostar Continued Pumping or Injecting Into Vein Combining With Gemcitabine-Carboplatin Versus Gemcitabine-Carboplatin Alone to Treat Non-Small Cell Lung Cancer (NSCLC)
- 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)
The purpose of this study is to determine whether Endostar with Gemcitabine-Carboplatin are more effective than Gemcitabine-Carboplatin alone in the treatment of Non-Small Cell Lung Cancer (NSCLC),and about Endostar ,Compared with intravenous, Continued vein-pumping maby is a more effective way.
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 |
|---|---|---|---|
| Non-small Cell Lung Cancer | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Gemcitabine,Carboplatin,Endostar | Drug | — | UNRESOLVED |
| Gemcitabine(G) Carboplatin(C) | Drug | — | UNRESOLVED |
| Gemcitabine(G) Carboplatin(C) Endostar | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- Endostar -Continued Pumping into+GC
- description
- Endostar that is Continued Pumping into vein Combining With Gemcitabine -Carboplatin
- interventionNames
- Drug: Gemcitabine,Carboplatin,Endostar
- type
- ACTIVE_COMPARATOR
- label
- Endostar -injecting into +GC
- description
- Endostar that is injecting into vein with Gemcitabine -Carboplatin
- interventionNames
- Drug: Gemcitabine(G) Carboplatin(C) Endostar
- type
- ACTIVE_COMPARATOR
- label
- GC
- description
- Gemcitabine -Carboplatin
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: 1. Histologically or cytologically diagnosed NSCLC; 2. primary treatment,inoperable stage III/IV NSCLC; 3. Age of 18-70years; Gender Not Required; 4. Adequate hematologic, renal, and hepatic function ,Specific index as follows: liver function: S-Bilirubin ≤1.5 ULN ; Transaminase≤2 ULN. renal function: S-Creatinine ≤1.2 ULN; blood urea nitrogen ≤1.2 ULN . ULN: upper normal limit. Marrow Hemopoietic Function: WBC≥4.0×10\^9/l, ANC≥2.0×10\^9/l platelet count ≥100×10\^9/l, Hb≥100 g/l; 5. ECOG PS 0-2,Life expectancy ≥ 3 months; endure more than two cycle chemotherapy; 6. The patients have explicit lung tumor lesions and the lesions were measurable; (According to the standard of RECIST1.1, they should have at least one of accurately measurable lesions with the largest diameter ≥ 10mm by spiral CT, MRI); 7. No history of serious drug allergy; 8. Informed consent should be obtained before treatment. Exclusion Criteria: 1. Symptomatic brain metastases with cognitive disorder,bone metastases with complications; 2. Major organ dysfunction and Serious Heart Disease( congestive heart-failure,incontrollable high-risk arrhythmia,unstable angina, valvular disease, myocardial infarct and Resistant hypertension,); 3. Serious complications and investigator consider it is unsuited enrolling; 4. Pregnant or lactating women; 5. Allergic to research drug; 6. participating in other experimental trials and receive the treatment in four weeks; 7. The position that is for observing curative effect have a radiotherapy.
References
Publications (0)
Data not yet available