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Lung Neoplasms clinical trials

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NCT ID: NCT00288054 Terminated - Lung Cancer Clinical Trials

S0429: Docetaxel, Cetuximab, and Radiation Therapy in Treating Patients With Stage III Non-Small Cell Lung Cancer

Start date: April 2006
Phase: Phase 1
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as cetuximab, can block tumor growth in different ways. Some find tumor cells and kill them or carry tumor-killing substances to them. Others interfere with the ability of tumor cells to grow and spread. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving docetaxel and cetuximab together with radiation therapy may kill more tumor cells. PURPOSE: This phase I trial is studying the side effects and best dose of docetaxel when given together with cetuximab and radiation therapy in treating patients with stage III non-small cell lung cancer.

NCT ID: NCT00286169 Terminated - Clinical trials for Small-cell Lung Cancer

Amrubicin Study for Elderly Patients With Extensive-disease Small-cell Lung Cancer (ED-SCLC)

Start date: April 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the efficacy and toxicity of amrubicin with carboplatin plus etoposide in elderly patients with extensive-disease small-cell lung cancer.

NCT ID: NCT00281827 Terminated - Lung Cancer Clinical Trials

Carboplatin, Gemcitabine, and Thalidomide in Patients Undergoing Surgery for Stage II or III Non-Small Cell Lung Cancer

Start date: May 2002
Phase: Phase 2
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as carboplatin and gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Thalidomide may stop the growth of tumor cells by blocking blood flow to the tumor. Giving carboplatin and gemcitabine together with thalidomide before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. PURPOSE: This phase II trial is studying how well giving carboplatin and gemcitabine together with thalidomide works in treating patients who are undergoing surgery for stage II or stage III non-small cell lung cancer.

NCT ID: NCT00281125 Terminated - Clinical trials for Non-Small Cell Lung Cancer and Pleural Mesothelioma

Phase I/II Trial of PTK787 and Pemetrexed With or Without Cisplatin for Lung Cancer

Start date: January 2006
Phase: Phase 1/Phase 2
Study type: Interventional

This is an open-label, two-arm, multicenter Phase IA/II dose-escalation study of PTK787 in combination with Pemetrexed alone (Cohort 1) or Pemetrexed and Cisplatin (Cohort 2). This study is designed to determine the maximum tolerated dose (MTD) and dose limiting toxicity (DLT) of PTK787 when administered in combination with Pemetrexed or Pemetrexed and Cisplatin, and to characterize the safety, tolerability, biologic activity, and PK profile of PTK787 in adult patients with advanced non-small cell lung cancers and mesotheliomas.

NCT ID: NCT00281021 Terminated - Clinical trials for Carcinoma, Non-Small Cell Lung

Second Line Erlotinib (Tarceva) Plus Digoxin in Non-Small Cell Lung Cancer

Start date: February 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the potential benefit of adding Digoxin to erlotinib (Tarceva) treatment for patients with non-small cell lung cancer.

NCT ID: NCT00280748 Terminated - Lung Cancer Clinical Trials

Whole-Brain Radiation Therapy and Pemetrexed in Treating Patients With Brain Metastases From Non-Small Cell Lung Cancer

NRR
Start date: May 2005
Phase: Phase 2
Study type: Interventional

RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. Pemetrexed may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving radiation therapy together with pemetrexed may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving whole-brain radiation therapy together with pemetrexed works in treating patients with brain metastases from non-small cell lung cancer.

NCT ID: NCT00277329 Terminated - Clinical trials for Non-small Cell Lung Cancer

Study of XL999 in Patients With Non-small Cell Lung Cancer

Start date: December 2005
Phase: Phase 2
Study type: Interventional

This clinical study is being conducted at multiple sites to determine the activity, safety, and tolerability of XL999 when given weekly to patients with non-small cell lung cancer (NSCLC). XL999 is a small molecule inhibitor of multiple kinases including VEGFR, PDGFR, FGFR, FLT-3, and Src, which are involved in tumor cell growth, formation of new blood vessels (angiogenesis), and metastasis.

NCT ID: NCT00273507 Terminated - Clinical trials for Non-small Cell Lung Cancer

Neoadjuvant Chemotherapy in Non Small Cell Lung Cancer (NSCLC) Stages IB, IIA, IIB, and IIIA/T3

Start date: January 1998
Phase: Phase 3
Study type: Interventional

Randomised trial of chemotherapy or not before surgery in early resectable stages of NSCLC (IB, IIA, IIB, and IIIA/N2).

NCT ID: NCT00271323 Terminated - Clinical trials for Non-Small-Cell Lung Carcinoma

Safety Study of Docetaxel/Cisplatin Induction Therapy Followed by Concurrent Chemoradiotherapy or Concurrent Chemoradiotherapy Followed by Consolidation Docetaxel/Cisplatin in NSCLC Patients

Start date: May 2005
Phase: Phase 2
Study type: Interventional

- Primary : To determine the safety profile of each treatment group. - Secondary : To determine efficacy in term of overall response, disease free survival and survival at 1 and 2 years.

NCT ID: NCT00269828 Terminated - NSCLC Clinical Trials

A Survival Study for Women With Advanced Lung Cancer Who Have Not Previously Received Chemotherapy.

PIONEER
Start date: December 2005
Phase: Phase 3
Study type: Interventional

This is a randomized, open-label, multinational, phase III study in women with histologically- or cytologically-confirmed advanced NSCLC who are chemotherapy naïve and have PS 2. Study drug will be administered on day 1 of each 21 day cycle