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Lung Neoplasms clinical trials

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NCT ID: NCT01928160 Withdrawn - Clinical trials for Stage IV Non-small Cell Lung Cancer

Pemetrexed Disodium and Carboplatin or Cisplatin With or Without Erlotinib Hydrochloride in Treating Patient With Stage IV Non-Small Cell Lung Cancer Resistant to First-Line Therapy With Erlotinib Hydrochloride or Gefitinib

Start date: June 2014
Phase: Phase 2
Study type: Interventional

This randomized phase II trial studies how well pemetrexed disodium and carboplatin or cisplatin with or without erlotinib hydrochloride work in treating patients with epidermal growth factor receptor (EGFR) mutant positive stage IV non-small cell lung cancer and acquired resistance to first-line therapy with erlotinib hydrochloride or gefitinib. In patients that develop resistance to first-line therapy with EGFR tyrosine kinase inhibitors (TKIs) the drug is usually stopped and the patient is switched to chemotherapy. Drugs used in chemotherapy, such as pemetrexed disodium, carboplatin, and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Erlotinib hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. It is not yet known whether pemetrexed disodium and carboplatin or cisplatin is more effective with or without erlotinib hydrochloride in treating patients with EGFR mutant non-small cell lung cancer and acquired resistance to EGFR TKIs.

NCT ID: NCT01925625 Completed - Lung Cancer Clinical Trials

Early Cancer Detection Test - Lung Cancer Scotland

ECLS
Start date: August 2013
Phase: N/A
Study type: Interventional

HYPOTHESIS In a high risk population the EarlyCDT-Lung test reduces the incidence of late stage tumours;3 / 4 / Unclassified (U) at diagnosis compared to normal clinical practice.

NCT ID: NCT01924416 Completed - Clinical trials for Non-Small-Cell Lung Cancer

Lung Cancer Information Study (LCIS-R01)

LCIS-R01
Start date: September 2012
Phase: N/A
Study type: Interventional

The primary specific aim is to test the hypothesis that use of a decision aid to enhance informed, shared decision making coupled with quality of life assessment in patients with advanced lung cancer receiving first-, second-, or third-line therapy will lead to a reduction in two major contributors of cost (number of chemotherapy cycles; number of advanced imaging studies) compared with the control arm.

NCT ID: NCT01924195 Completed - Clinical trials for Non-small Cell Lung Cancer

Phase II Study of Anlotinib in Patients With Advanced Non-small Cell Lung Cancer(ALTER0302)

Start date: August 2013
Phase: Phase 2
Study type: Interventional

Anlotibib (AL3818) is a kind of innovative medicines approved by State Food and Drug Administration(SFDA:2011L00661) which was researched by Jiangsu Chia-tai Tianqing Pharmaceutical Co., Ltd. Anlotinib is a kinase inhibitor of receptor tyrosine with multi-targets, especially for VEGFR2、VEGFR3、PDGFRβ and c-Kit. It has the obvious resistance to new angiogenesis. The trial is to explore Anlotinib for the effectiveness and safety of andvanced non-small cell lung cancer who failed two lines of chemotherapy

NCT ID: NCT01922583 Completed - Clinical trials for Non-small Cell Lung Cancer (NSCLC)

AUY922 in Patient With Stage IV NSCLC

NSCLC
Start date: January 2014
Phase: Phase 2
Study type: Interventional

This is an open-label, single-arm, multicenter phase II trial in patients with stage IV EGFR T790M, EGFR exon 20 and other uncommon, HER2, or BRAF-mutated; ALK, ROS1, or RET-rearranged NSCLC.

NCT ID: NCT01920789 Active, not recruiting - Clinical trials for Non-small Cell Lung Cancer

Stereotactic Precision And Conventional Radiotherapy Evaluation

SPACE
Start date: January 2007
Phase: N/A
Study type: Interventional

A randomized phase II study for medically inoperable stage I non-small cell lung cancer where stereotactic body radiotherapy in three fractions to 66 Gy is compared with conventionally fractionated radiotherapy to 70 Gy in 35 fractions.

NCT ID: NCT01918761 Terminated - Clinical trials for Non Small Cell Lung Cancer

Dacomitinib + Pemetrexed for Patients With Advanced Non-squamous Non-small Cell Lung Cancer (NSCLC)

Start date: July 30, 2013
Phase: Phase 1
Study type: Interventional

To identify a dose of dacomitinib in combination with pemetrexed that is safe and tolerated as determined by the incidence of DLTs (dose limiting toxicities).

NCT ID: NCT01915524 Terminated - Clinical trials for Non-Small Cell Lung Carcinoma

Trial of RNActive®-Derived Cancer Vaccine and Local Radiation in in Stage IV Non Small Cell Lung Cancer (NSCLC)

Start date: April 2013
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine whether the new RNActive derived lung cancer vaccine CV9202 in combination with local radiation therapy is safe, tolerable and immunogenic for the consolidation and maintenance treatment of stage IV non small cell lung cancer (NSCLC) after first-line chemotherapy or therapy with an EGFR tyrosine kinase inhibitor.

NCT ID: NCT01914458 Recruiting - Lung Cancer Clinical Trials

Image Discovering Early Lung Cancer Project

IDEALCAP
Start date: February 2013
Phase: Phase 2
Study type: Interventional

Lung cancer is the leading cause of cancer related death in Taiwan and world wide. The application of low dose helical computed tomography (CT) has been the milestone of lung cancer screening. Recently, The National Lung Screening Trial (NLST) shows screening with low-dose CT could reduce mortality from lung cancer. We conducted this clinical trial to determine the efficacy of low dose CT in early lung cancer screening in Taiwan.

NCT ID: NCT01914120 Recruiting - Lung Cancer Clinical Trials

the Quality of Life Assessment of Lung Cancer Patients in China

Start date: November 2012
Phase: N/A
Study type: Observational

The goal of this study is assess the quality of life of advanced non-small cell lung cancer (NSCLC) patients who are undergoing first-line chemotherapy, analyze the current status and tendency of quality of life (QOL). The method is to use the Functional Assessment of Cancer Therapy-Lung (FACT-L) scales, assess the quality of life before the chemotherapy, after 1st cycle of chemotherapy and after 2nd cycle. After 3 time-points, investigators analyze all the subscales and constructs of FACT-L. The assumption is the quality of life will be better after 2 cycle of chemotherapy.