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Small Cell Lung Carcinoma clinical trials

View clinical trials related to Small Cell Lung Carcinoma.

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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: 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: NCT01591512 Terminated - Clinical trials for Small Cell Lung Cancer

A Prospective Longitudinal Collection of Subjects Diagnosed With Small Cell Lung Cancer

Start date: May 2011
Phase: N/A
Study type: Observational

The purpose of this study is to collect samples to evaluate the ProGRP and NSE assays independently as aids for monitoring the course of disease and therapy in subjects diagnosed with SCLC.

NCT ID: NCT01575782 Terminated - Clinical trials for Small Cell Lung Cancer

Chloroquine as an Anti-autophagic Radiosensitizing Drug in Stage I-III Small Cell Lung Cancer

Chloroquine
Start date: May 2014
Phase: Phase 1
Study type: Interventional

Chloroquine can make tumor cells less resistant to chemo/radiotherapy. In this trial chloroquine is given during radiotherapy. The dose is increased in cohorts of at least 3 patients.

NCT ID: NCT01574300 Terminated - Clinical trials for Small Cell Lung Carcinoma

Collaborative Advanced Stage Tissue Lung Cancer (CASTLE) Network

CASTLE
Start date: November 2010
Phase:
Study type: Observational

The purpose of this study is to facilitate application of the known biomarkers to patients presenting today, and to establish a collection of biospecimens that will be useful for discovering and validating new biomarkers for future use.

NCT ID: NCT01573338 Terminated - Clinical trials for Small Cell Lung Carcinoma

Clinical Study to Evaluate the Maximum Tolerated Dose of BAY1000394 When Given Together With Chemotherapy and the Effectiveness of This Combination Treatment in Shrinking a Specific Type of Lung Tumors (Small Cell Lung Cancer)

Start date: February 25, 2013
Phase: Phase 1/Phase 2
Study type: Interventional

This is the first study where BAY1000394 is given in combination with chemotherapy: cisplatin / etoposide or carboplatin / etoposide. Patients with small cell lung cancer will be treated. Every patient will receive drug treatment, there is no placebo group. Different groups of patients will receive different dosages of BAY1000394 to determine the safety and maximum tolerated dose (MTD) of BAY1000394 in combination with chemotherapy. The dose of chemotherapy is the standard dose usually administered and will not change. The study will also assess how the drug is metabolized by the body and changes in tumor size. BAY1000394 will be given per mouth, twice a day for three days every week. Treatment will stop if the tumor continues to grow, if side effects occur which the patient can not tolerate or if the patients decides to exit treatment.

NCT ID: NCT01487499 Terminated - Clinical trials for Small Cell Lung Cancer

Bronchoscopic Intratumoral Chemotherapy for Small Cell Lung Cancer (SCLC)

SCLC
Start date: December 2011
Phase: Phase 3
Study type: Interventional

This project proposes to use bronchoscopic intratumoral chemotherapy for small cell lung cancer in two fashions: 1. to implement a prospective clinical trial to test the feasibility and efficacy of intralesional chemotherapy as consolidative therapy immediately following standard systemic chemotherapy and radiation therapy for patients with limited stage SCLC by comparing tumor growth and survival rates of the treatment group and compare the outcomes to historical controls 2. to implement a prospective clinical trial to test the feasibility and efficacy as measured by tumor growth and survival rates of intralesional chemotherapy for patients with recurrent SCLC after standard treatment.

NCT ID: NCT01486459 Terminated - Clinical trials for Small Cell Lung Cancer

A Feasibility Trial Using Lithium As A Neuroprotective Agent In Patients Undergoing Prophylactic Cranial Irradiation For Small Cell Lung Cancer

TULIP
Start date: November 2012
Phase: N/A
Study type: Interventional

Small cell lung cancer is an aggressive neuroendocrine tumour that often presents with extensive (metastatic) disease. Chemotherapy is the mainstay of treatment, with radiotherapy to the primary tumour. It is now part of care to also offer Prophylactic Cranial Irradiation (PCI) in order to prevent spread of the cancer into the brain. Cognitive impairment can result after cranial irradiation. Lithium is thought to be neuroprotective. It is hypothesized that lithium administration with PCI will be safe, tolerable and feasible, and can be studied to prevent or ameliorate the ensuing cognitive impairment.

NCT ID: NCT01421316 Terminated - Clinical trials for Small Cell Lung Cancer

Hair-sparing Whole Brain Radiotherapy

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

Up to 10% of patients with cancer will develop symptomatic brain metastases. Given this limited survival it is important to consider quality of life (QOL) when treating these patients. Whole brain radiotherapy (WBRT) can increase survival to 6 month. However, WBRT itself has been shown to reduce QOL by increasing drowsiness, leg weakness and hair loss in patients with brain metastases. Both fatigue and hair loss were reported to have the largest decline in QOL scores when WBRT is used in the prophylactic setting in small cell lung cancer. Recent technological improvements in patient positioning and treatment planning will allow us to treat the whole brain with reduced margins, allowing better sparing of the scalp. In view of the large impact of hair loss on quality of life, the investigators hypothesize to see an improved quality of life with scalp sparing techniques. Study hypothesis: Volumetric arc therapy results in a reduced hair loss and a subsequent clinically important improvement in QOL.

NCT ID: NCT01392352 Terminated - Breast Cancer Clinical Trials

HYPAZ: Hypertension Induced by Pazopanib

HYPAZ
Start date: April 2011
Phase: Phase 2
Study type: Interventional

Pazopanib is a new cancer drug that works by limiting the growth of new blood vessels in tumours. About half of patients who take pazopanib develop high blood pressure (hypertension). This side effect can make patients have to reduce or stop their cancer treatment, and can cause other health problems. The aim of this study is to find out exactly how the drug causes high blood pressure.