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Neoplasm Metastasis clinical trials

View clinical trials related to Neoplasm Metastasis.

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NCT ID: NCT02560311 Recruiting - Breast Cancer Clinical Trials

Long-term Outcome of HER2-amplified Metastatic Breast Cancer: A Retrospective Analysis

Start date: December 2014
Phase: N/A
Study type: Observational

The aim of this study is to analyze cases of human epidermal growth factor receptor (HER) 2-positive metastatic breast cancer (MBC) of the last 10 years at the University Hospital of Zurich to assess the efficacy of the treatment with trastuzumab in HER2-positive MBC and to find out associations between different variables and the outcome. The aim is to find out probable prognostic factors and patterns of disease progression. Prognostic factors could optimize treatment approaches and result in a delay of disease progression.

NCT ID: NCT02557490 Recruiting - Clinical trials for Colon Cancer Liver Metastasis

Oxaliplatin and Raltitrexed Treatment of Colorectal Cancer With Liver Metastases

Start date: January 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study was a randomized controlled trial to compare the effect of oxaliplatin and raltitrexed treatment of colorectal cancer with liver metastases by TACE hepatic artery infusion

NCT ID: NCT02553707 Completed - Clinical trials for Pain; Bone Neoplasms; Neoplasm Metastasis

A Study to Assess the Short Term Efficacy of Intravenous Ibandronate (Bondronat) in Participants With Metastatic Bone Pain Due to Breast Cancer

Start date: July 2006
Phase: Phase 4
Study type: Interventional

This study will assess the short term efficacy of ibandronate (6 mg intravenous [IV]) in participants with breast cancer and malignant bone disease, with moderate to severe pain. All participants will receive an IV infusion of ibandronate on Days 1, 2, and 3, and pain response will be measured on Days 1-7. The anticipated time on study treatment is 3 days, and the target sample size is 182 individuals.

NCT ID: NCT02549417 Completed - Clinical trials for Secondary Hyperparathyroidism

Phase 3 Study of KHK7580

Start date: September 29, 2015
Phase: Phase 3
Study type: Interventional

This study is designed to evaluate efficacy and safety of KHK7580 orally administered once daily for 32 weeks for patients with secondary hyperparathyroidism receiving peritoneal dialysis. After 32-week treatment period, the subjects will receive KHK7580 in the 20-week extension period to evaluate long-term safety and efficacy.

NCT ID: NCT02549404 Completed - Clinical trials for Secondary Hyperparathyroidism

Phase 3 Study of KHK7580

Start date: September 28, 2015
Phase: Phase 3
Study type: Interventional

This long-term study is designed to evaluate safety and efficacy of KHK7580 orally administered once daily for 52 weeks for patients with secondary hyperparathyroidism receiving hemodialysis.

NCT ID: NCT02549391 Completed - Clinical trials for Secondary Hyperparathyroidism

Phase 3 Study of KHK7580

Start date: September 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of KHK7580 orally administered once daily for 30 weeks in subjects with secondary hyperparathyroidism (SHPT) receiving hemodialysis in a randomized, double-blind, intra-subject dose-adjustment, parallel-group design with cinacalcet hydrochloride as an active control.

NCT ID: NCT02547805 Completed - Nephrolithiasis Clinical Trials

Evaluate the Effect of ALLN-177 in Reducing Urinary Oxalate in Patients With Secondary Hyperoxaluria and Kidney Stones Over 28 Days

Start date: September 2015
Phase: Phase 2
Study type: Interventional

Evaluate the safety, tolerability, and efficacy of 28 days of treatment with ALLN-177 for reducing urinary oxalate excretion in patients with secondary hyperoxaluria and kidney stones.

NCT ID: NCT02545309 Active, not recruiting - Clinical trials for Secondary Sclerosing Cholangitis

Secondary Sclerosing Cholangitis in Critically Ill Patients

SSC-CIP
Start date: December 21, 2015
Phase:
Study type: Observational

SSC-CIP is increasing in patients after critical illness. Pathogenesis is still largely unclear. The investigators hypothesize that genetic variants of biliary transporter genes are frequent in patients with SSC-CIP. In approximately 140 patients and controls the rate of genetic variants in biliary transporter genes, gut permeability and gut microbiome as well as bone health will be studied.

NCT ID: NCT02537600 Completed - Malignant Melanoma Clinical Trials

Vemurafenib and Cobimetinib Combination in BRAF Mutated Melanoma With Brain Metastasis

CONVERCE
Start date: December 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine wether cobimetinib + vemurafenib combination treatment is effective in the treatment of BRAFV600-mutated melanoma patients with brain metastasis

NCT ID: NCT02533115 Approved for marketing - Secondary AML Clinical Trials

EAP of CPX-351 (VYXEOS) for Patients 60-75 Years of Age With Secondary AML

401
Start date: n/a
Phase: N/A
Study type: Expanded Access

This study is a Phase IV Expanded Access Protocol (EAP) of CPX-351 in patients with secondary acute myeloid leukemia who are suitable for treatment with intensive chemotherapy.