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Lung Neoplasms clinical trials

View clinical trials related to Lung Neoplasms.

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NCT ID: NCT01723878 Completed - Clinical trials for Non-Squamous Non-Small Cell Lung Cancer

ASPET Study: An Observational Study of Tarceva (Erlotinib) in First Line in Patients With Advanced Non-Small Cell Lung Cancer Harbouring EGFR Activating Mutations

Start date: December 30, 2013
Phase: N/A
Study type: Observational

This observational study will evaluate the patterns of disease progression in patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) harbouring EGFR activating mutations receiving Tarceva (erlotinib) as first-line treatment. Patients will be followed for up to 12 months after progression of disease.

NCT ID: NCT01723800 Completed - Clinical trials for Stage IV Non-small Cell Lung Cancer

PI3K Inhibitor BKM120, Carboplatin, and Pemetrexed Disodium in Treating Patients With Stage IV Non-Small Cell Lung Cancer

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

This phase I trial studies the side effects and best dose of PI3K inhibitor BKM120 when given together with carboplatin and pemetrexed disodium in treating patients with stage IV non-small cell lung cancer. PI3K inhibitor BKM120 and pemetrexed disodium may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as carboplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving PI3K inhibitor BKM120, carboplatin, and pemetrexed disodium together may kill more tumor cells

NCT ID: NCT01722292 Terminated - Clinical trials for Small Cell Lung Carcinoma

A Study of LY2940680 in Small Cell Lung Cancer

Start date: January 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to find a recommended dose of LY2940680 that can be safely given in combination with etoposide and carboplatin followed by LY2940680 alone in participants with extensive-disease small cell lung cancer. The study will also compare progression-free survival in participants who are administered etoposide, carboplatin and LY2940680 followed by LY2940680 alone versus etoposide, carboplatin, and placebo followed by placebo alone.

NCT ID: NCT01721759 Completed - Clinical trials for Squamous Cell Non-small Cell Lung Cancer

Study of Nivolumab (BMS-936558) in Patients With Advanced or Metastatic Squamous Cell Nonsmall-cell Lung Cancer Who Have Received At Least 2 Prior Systemic Regimens

Start date: November 16, 2012
Phase: Phase 2
Study type: Interventional

The purpose of the study is to assess the objective response rate (change in tumor size from baseline) in patients with advanced or metastatic squamous cell nonsmall-cell lung cancer treated with Nivolumab (BMS-936558) after failure of 2 prior systemic regimens

NCT ID: NCT01721252 Completed - Clinical trials for Non-small Cell Lung Cancer

Tarceva. ICORG 08-41

Start date: December 2009
Phase: N/A
Study type: Observational

The aim of this study is to determine prospectively the value of a recently identified proteomic signature in identifying those patients with lung cancer, who are likely to benefit from and respond favourably to erlotinib therapy. This is a prospective study of serum proteomics as a predictor of response to erlotinib therapy.

NCT ID: NCT01720901 Suspended - Clinical trials for Non-small Cell Lung Cancer

Increased Dose of Icotinib in Advanced None Small Cell Lung Cancer Patients After Routine Gefitinib Therapy

Start date: February 2013
Phase: Phase 4
Study type: Interventional

To evaluate the efficacy and safety of increased dose of icotinib in advanced NSCLC patients who progressed after gefitinib therapy.

NCT ID: NCT01720836 Recruiting - Clinical trials for Non-small Cell Lung Cancer (NSCLC)

Study of the Immune Response of MUC1 (Mucin1) Peptide Vaccine for Non-small Cell Lung Cancer

Start date: November 2012
Phase: Phase 1/Phase 2
Study type: Interventional

All subjects will receive the vaccine subcutaneously every 3 weeks x 3 with optional yearly booster vaccines up to and including 5 years post last vaccine for those patients who are confirmed responders to the vaccine . The rationale for using Poly-ICLC as an adjuvant are two ongoing trials at University of Pittsburgh Cancer Institute (UPCI) of the MUC1 100mer peptide vaccine - one as a therapeutic vaccine in subjects with metastatic castrate resistant prostate cancer and the other in subjects with advanced colonic adenomas at risk for developing colon cancer. The same formulation, MUC1 100mer peptide admixed with Poly-ICLC, is used in both trials. There has been no toxicity observed and the vaccine is highly immunogenic in early disease. In the proposed NSCLC trial the anti-MUC1 immune response will be thoroughly characterized.

NCT ID: NCT01720186 Terminated - Clinical trials for Non Small Cell Lung Cancer

Evaluation of a Pneumotachograph (SPI) for the Production of PET and CT Acquisitions Synchronized With Breath for the Assessment of Extension of Lung Cancer

SPI COHERENCE
Start date: May 2013
Phase: N/A
Study type: Interventional

This is a pilot study, single-center, prospective, open-label, to assess the acceptability and performance of the experimental medical device (SPI) used during an imaging examination (PET / CT 4D imaging in synchronized mode centered on the thorax). Each patient will be its own control, since the imaging examination will be synchronized simultaneously with the two systems: tested Medical Device (SPI) and reference Medical Device(RPM).

NCT ID: NCT01719861 Terminated - Clinical trials for Small Cell Lung Cancer

Phase IIa Desipramine in Small Cell Lung Cancer and Other High-Grade Neuroendocrine Tumors

Start date: October 2012
Phase: Phase 2
Study type: Interventional

Intrapatient dose escalation of desipramine. Start at 75 mg daily. Increase by 75 mg weekly to maximum of 450 mg daily. Taper desipramine upon disease progression, unacceptable toxicity or patient withdrawal from study.

NCT ID: NCT01719068 Recruiting - Lung Cancer Clinical Trials

Early Detection of Lung Cancer and Mesothelioma in Workers Exposed to Asbestos

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

This is a pilot study that aims to develop a lung cancer screening program for workers in British Columbia, Canada exposed to asbestos who are at risk of developing lung cancer/pleural mesothelioma. This is high risk population is at of respiratory system diseases as a result of their occupational exposures. Additionally, knowledge garnered from this study will allow us to develop other studies that will further our understanding of asbestos related lung cancer and mesothelioma.