Clinical trial · Interventional
Study of Carboplatin/Gemcitabine Plus Bevacizumab in Advanced Lung Cancer
Phase II Trial of Carboplatin/Gemcitabine Plus Bevacizumab in Advanced Non-Small Cell Lung Cancer
- 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)
* this study is being done to find out if the combination of carboplatin and gemcitabine will be more effective in the the treatment of advanced lung cancer if bevacizumab, an agent that blocks tumor blood vessel formation, is added * the study will measure the time to progression of patients treated with the combination; we hope to show that the addition of bevacizumab improves the time to progression (increases the amount of time before the disease begins to worsen) * all patients receive all three drugs; there is no placebo
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 |
|---|---|---|---|
| bevacizumab | Drug | Bevacizumab | ALIAS |
| carboplatin | Drug | Carboplatin | ALIAS |
| gemcitabine | Drug | Gemcitabine | ALIAS |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- time to progression
Secondary outcomes (5)
- measure
- response rate
- measure
- median survival
- measure
- one year survival
- measure
- two year survival
- measure
- toxicity
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Histologically or cytologically proven non-small cell lung cancer, newly diagnosed or recurrent after previous surgery and/or radiation therapy * Stage IV disease or stage IIIB with a malignant pleural effusion * measurable or evaluable disease * Performance status 0 or 1 (ECOG) * adequate renal, hepatic, and bone marrow function * adequate recovery from previous surgery or radiotherapy * informed consent Exclusion Criteria: * brain metastases * squamous (epidermoid) histology * hemoptysis * central airway disease * Pancoast tumors * previous chemotherapy or biologic therapy for lung cancer * prior malignancy within the previous 5 years except non-melanoma skin cancer or cervical CIS * pregnant or nursing women
References
Publications (0)
Data not yet available