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Lung Neoplasms clinical trials

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NCT ID: NCT00684385 Approved for marketing - Clinical trials for Non Small Cell Lung Cancer

An Expanded Access Programme With Iressa for Patients With Non-Small-Cell Lung Cancer and Cancer of the Head and Neck

Start date: n/a
Phase:
Study type: Expanded Access

The purpose of this study is to provide ZD1839 for those patients with locally advanced and/or metastatic non-operable non-small cell lung cancer (stage III or IV) or recurrent and/or metastatic squamous cell head and neck cancer who receive the therapy on an expanded access basis due to their inability to meet eligibility criteria for on-going recruiting trials, inability to participate in other clinical trials (e.g., poor performance status, lack of geographic proximity), or because other medical interventions are not considered appropriate or acceptable.

NCT ID: NCT00683904 Completed - Clinical trials for Non-small Cell Lung Cancer (NSCLC)

Ixabepilone in Combination With Carboplatin in Patients With Non-small Cell Lung Cancer

Start date: June 2008
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the maximum tolerated dose, dose-limiting toxicity, and recommended Phase II dose of ixabepilone in combination with carboplatin in patients with non-small cell lung cancer.

NCT ID: NCT00682981 Completed - Clinical trials for Extensive-stage Small Cell Lung Cancer

A Phase I/II Study of Carboplatin and Etoposide With or Without Obatoclax in Extensive-stage Small Cell Lung Cancer (ES-SCLC)

Start date: May 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The Phase I portion of this protocol will determine the best phase II dose and schedule of obatoclax with carboplatin and etoposide in patients with extensive-stage small cell lung cancer. The Phase II portion will evaluate the response rate to this regimen.

NCT ID: NCT00682032 Recruiting - Clinical trials for Non Small Cell Lung Cancer

The Effect of Beta-glucan in Non-Small Cell Lung Cancer

Start date: October 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine how beta-glucan affects the immune system in subjects with non-small cell lung cancer.

NCT ID: NCT00681512 Terminated - Clinical trials for Non Small Cell Lung Cancer

The Effect of Berries on Lung Cancer Tumors

Start date: April 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine how berries affect cancer tumors in patients with non-small cell lung cancer.

NCT ID: NCT00680940 Completed - Clinical trials for Non Small Cell Lung Cancer

A Study of Mycobacterium w in Combination With Paclitaxel Plus Cisplatin in Advanced Non Small Cell Lung Cancer

NSCLC
Start date: June 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether Mycobacterium w in combination with Paclitaxel plus Cisplatin are effective in Advanced Non Small Cell Lung cancer.

NCT ID: NCT00678964 Recruiting - Clinical trials for Non-Small Cell Lung Cancer

Erlotinib Versus Carboplatin/Vinorelbine in Elderly Patients With Advanced Non-Small Cell Lung Cancer (NSCLC)

TIE
Start date: June 2006
Phase: Phase 2
Study type: Interventional

60% of all malignant diseases occur in patients who are 65 years or older. For these patients, aggressive treatments are often not suitable due to reduced life-expectancy, reduced general condition, comorbidities, and reduced vital functions which can lead to increased adverse effects of chemotherapy. Therefore, it is important to investigate alternative therapy options for elderly patients. Erlotinib is an orally applied medication which is associated with reasonable toxicity. This targeted agent may prove an effective and well-tolerated first-line therapy in elderly patients with advanced non small cell lung cancer. Therefore, the aim of this study is to investigate the progression-free survival of the combination of vinorelbine and carboplatin in comparison to erlotinib. Given that there will be no significant reduction of efficiency this may provide elderly patients of more than 70 years of age with an active oral substance without subjecting them to the sometimes severe adverse effect of the chemotherapy.

NCT ID: NCT00676507 Completed - Lung Neoplasm Clinical Trials

Phase III Lucanix™ Vaccine Therapy in Advanced Non-small Cell Lung Cancer (NSCLC) Following Front-line Chemotherapy

STOP
Start date: July 2008
Phase: Phase 3
Study type: Interventional

Rationale: Vaccines made from gene-modified tumor cells may help the body build an immune response to kill tumor cells. It is not yet known whether vaccine therapy is more effective than a placebo as maintenance therapy in treatment of subjects with non-small cell lung cancer. Purpose: This randomized phase III trial is studying vaccine therapy to see how well it works compared with a placebo in treating subjects with stage III or stage IV non-small cell lung cancer.

NCT ID: NCT00675597 Completed - Lung Cancer Clinical Trials

Docetaxel (Taxotere), Vinorelbine, and Bevacizumab, as Adjuvant Chemotherapy for Patients With Resected Stage I-III Non-small Cell Lung Cancer

Start date: May 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether a combination of the drugs docetaxel (Taxotere ® ), plus vinorelbine (Navelbine ® ), will result in fewer side effects than cisplatin chemotherapy, thereby improving delivery of chemotherapy in patients. Another purpose of this study is to determine whether a third drug, bevacizumab (Avastin®), may be delivered safely with docetaxel plus vinorelbine in patients who are eligible to receive bevacizumab.

NCT ID: NCT00675168 Recruiting - Lung Cancer Clinical Trials

Positron Emission Tomography (PET)/Computed Tomography (CT) and Roentgen in Lung Cancer: Evaluation of Patients in General Practice

PROLOG
Start date: May 2008
Phase: Phase 4
Study type: Interventional

The prognosis of lung cancer depends much on the stage of the disease at the time of diagnosis. Only 16 % of lung cancer can be offered curative intended surgery. Chest x-ray is the gate-keeper in lung cancer diagnosis, but it has a miss rate of 20-60 %. A false negative chest x-ray often causes prolonged delay in diagnosis - often months. Recently a "48 hour diagnosis guaranty" has been implemented, which helps accelerate the system delay (delay from referral to diagnosis). But chest x-ray is still the gate-keeper; if the chest x-ray is negative further examination ceases. PET/CT has a higher sensitivity (96 %), than chest x-ray. In the latter years only little improvement in the survival rate of lung cancer has been made. Screening studies is currently been performed, but it's time for innovative thinking. PET/CT has established its place in the staging of lung cancer. But studies like this may help to place PET/CT in the chain of examination making it more cost-beneficial. The overall aim of this study is to improve patient course with earlier diagnosis of lung cancer.