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NCT ID: NCT00429039 Terminated - Clinical trials for ALLOGENEIC HEMATOPOIETIC STEM CELL TRANSPLANTATION

A Study to Accelerate Immune System Recovery Following Stem Cell Transplantation

Start date: September 2000
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if pre-treating donor lymphocytes with an investigational drug known as L-leucyl-L-leucine methyl ester (LLME, prior to donor lymphocyte infusion (DLI) will improve the recovery of the immune system following stem cell transplant.

NCT ID: NCT00427973 Terminated - Clinical trials for Advanced Adult Primary Liver Cancer

AZD2171 in Treating Patients With Locally Advanced Unresectable or Metastatic Liver Cancer

Start date: May 2009
Phase: Phase 2
Study type: Interventional

This phase II trial is studying how well AZD2171 works in treating patients with locally advanced unresectable or metastatic liver cancer. AZD2171 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor

NCT ID: NCT00427583 Terminated - Clinical trials for Malignant Peripheral Nerve Sheath Tumors

Imatinib Mesylate Treatment of Patients With Malignant Peripheral Nerve Sheath Tumors

Start date: May 2006
Phase: Phase 2/Phase 3
Study type: Interventional

This study assesses the safety and efficacy of imatinib mesylate treatment of patients with malignant peripheral nerve sheath tumors

NCT ID: NCT00419536 Terminated - Clinical trials for Hormone Refractory Prostate Cancer Disease

Safety of LBH589 Alone and in Combination With Intravenous Docetaxel and Prednisone

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

This 2-arm study is designed to determine the maximum tolerated dose of LBH589 as a single agent and in combination with docetaxel and prednisone 5 mg twice daily (second arm) and to characterize the safety, tolerability, biologic activity and pharmacokinetic profile.

NCT ID: NCT00417833 Terminated - Clinical trials for Choroidal Neovascularization

Multifocal Electrophysiologic Findings After Intravitreal Bevacizumab(Avastin)Treatment

Start date: December 2005
Phase: Phase 2/Phase 3
Study type: Interventional

Purpose: Determine the short-term safety of intravitreal bevacizumab by multifocal electroretinography (mf-ERG). Methods: 120 eyes with choroidal neovascularization, proliferative diabetic retinopathy and retinal vein occlusion received intravitreal bevacizumab (2.5mg/0.1cc). All patients underwent best corrected visual acuity, fluorescein angiography, optical coherent tomography and mf-ERG before and 1 month after treatment.

NCT ID: NCT00416793 Terminated - Clinical trials for Stage IV Pancreatic Cancer

Bortezomib and Carboplatin in Treating Patients With Metastatic Pancreatic Cancer

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

This phase II trial is studying how well giving bortezomib together with carboplatin works in treating patients with metastatic pancreatic cancer. Bortezomib 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 bortezomib together with carboplatin may kill more tumor cells.

NCT ID: NCT00415272 Terminated - Clinical trials for Fibrotic Interstitial Lung Disease

Pulmonary Rehabilitation in Patients With Fibrotic Interstitial Lung Disease

Start date: n/a
Phase: N/A
Study type: Interventional

Our study aims to investigate the benefits of an outpatient pulmonary rehabilitation program in a population of subjects with fibrotic interstitial lung disease. Our hypothesis is that pulmonary rehabilitation will lead to improvements in quality of life, breathlessness, exercise capacity and pulmonary function in this patient population.

NCT ID: NCT00412776 Terminated - Clinical trials for Head and Neck Cancer

Study of Proxinium Plus Best Supportive Care Versus Best Supportive Care for Patients With Advanced Head and Neck Cancer

Start date: December 2005
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to compare the safety and efficacy of Proxinium plus best supportive care with best supportive care only for patients with squamous cell head and neck cancer.

NCT ID: NCT00411801 Terminated - Clinical trials for Thrombotic Thrombocytopenic Purpura (TTP)

Safety and Efficacy Study to Compare Uniplas With Cryosupernatant Plasma in Thrombotic Thrombocytopenic Purpura (TTP)

Start date: May 2007
Phase: Phase 3
Study type: Interventional

Prior to the use of plasma products, thrombotic thrombocytopenic purpura (TTP) was usually a fatal condition. During plasma exchange therapy, patients need transfusion plasma that is blood group specific. Transfusing a patient with an incorrect blood group may have fatal consequences. Uniplas is a universally applicable human plasma, which can be administered irrespective of the patient's blood group. This study will test the safety and efficacy of Uniplas in comparison to cryosupernatant plasma in treatment of patients with TTP.

NCT ID: NCT00408252 Terminated - Recurrent Disease Clinical Trials

Efficacy of SU 011248 in Head And Neck Carcinoma

Start date: February 2007
Phase: Phase 2
Study type: Interventional

Preclinical studies as well as phase I and II trials have demonstrated that SU11248 has antitumor activity in renal cell carcinoma, breast cancer, neuroendocrine tumor and GIST. So at the light of these pre-clinical and clinical data, it seems interesting and promising to test SU011248 in these poor prognosis patients.