Clinical trial · Interventional
Alternating Cycles of Carboplatin/Gemcitabine and Carboplatin/Taxol for Advanced Stage NSCLC
Treatment of Stages IIIB and IV, Non Small Cell Lung Cancer With Alternating Cycles of Carboplatin/Taxol and Carboplatin/Gemcitabine.
NCT00259675CI-TRIAL-00000976completedPhase 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)
To see the efficacy of using chemotherapies alternatively (carboplatin and gemcitabine alternating with carboplatin and taxol) for pts with stage IIIB (nonresectable and stage IV NSCLC.
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 (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| carboplatin/gemcitabine, carboplatin/taxol | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- clinical response
Secondary outcomes (3)
- measure
- progression free survival
- measure
- 1 year survival
- measure
- safety and tolerability of regimen
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 19 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. Histologically/cytologically documented Non Small Cell Lung Carcinoma. 2. Stages IIIB and IV disease, not a candidate for definitive treatment with surgery, radiation or radiation plus chemotherapy. (Palliative radiotherapy will be allowed). 3. Age ≥ 18, \< 75 years. 4. ECOG performance status 2 5. No serious concomitant psychiatric illness. 6. Informed consent. 7. Presence of measurable or evaluable disease on physical examination, CT scan, chest x-ray, ultrasound or MRI scan. \- Exclusion Criteria: 1 ) Previous chemotherapy for NSCLC. 2\) Known CNS metastases at time of registration. 3\) Laboratory values obtained \<28 days prior to entry ANC \<1.5 x 109 /L PLT \<100 x 109 /L HgB\<100 g/L Total bili \>1.5 x UNL (upper normal limit) Alk PO4 \>3 x UNL AST \>3x UNL Cr \>1.5 x UNL. 4\) Uncontrolled diabetes mellitus, cardiovascular disease, active serious infection or other disease which in the opinion of treating physician, would make this protocol unreasonably hazardous for the patient. 5\) Known HIV positive. 6\) Palliative radiotherapy to only area of measurable disease. 7\) Prior malignancy, except for adequately treated basal cell or squamous cell skin cancer, adequately treated non invasive carcinomas, or other cancer from which the patient has been disease free for at least five years. 8\) Pregnant or nursing women. Men or women of childbearing potential who are unwilling to employ adequate contraception (condoms, diaphragm, birth control pills, injections, IUD, abstinence, surgical sterilization etc).
References
Publications (0)
Data not yet available
No reference posted for this study.