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Neoplasm Metastasis clinical trials

View clinical trials related to Neoplasm Metastasis.

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NCT ID: NCT02282813 Completed - Clinical trials for Chronic Kidney Disease

Extension Study of CTAP101-CL-3001 or CTAP101-CL-3002

Start date: April 2013
Phase: Phase 3
Study type: Interventional

This extension study of subjects previously enrolled in studies CTAP101-CL-3001 or CTAP101-CL-3002 allows long term evaluation of the safety and efficacy of CTAP101 Capsules in reducing elevated intact parathyroid hormone (iPTH) and correcting vitamin D insufficiency in stage 3 or 4 chronic kidney disease patients.

NCT ID: NCT02279992 Terminated - Glioma Clinical Trials

Pilot Study of Vardenafil and Carboplatin in Patients With Gliomas and Brain Metastases

LevitraCarbo
Start date: March 27, 2012
Phase: Early Phase 1
Study type: Interventional

This is a randomized pilot study to investigate the ability of a phosphodiesterase-V inhibitor (vardenafil) to increase the concentration of systemically delivered chemotherapy, carboplatin, in patients with recurrent malignant gliomas or metastatic brain cancer. This study will also determine the toxicity and tolerability of a phosphodiesterase-V inhibitor (vardenafil) in combination with intravenous carboplatin for patients with recurrent malignant gliomas or metastatic brain cancer.

NCT ID: NCT02277587 Completed - Clinical trials for Primary Adrenal Insufficiency

Dual RElease Hydrocortisone Versus conventionAl Glucocorticoid replaceMent Therapy in Hypocortisolism (DREAM)

DREAM
Start date: March 2014
Phase: Phase 4
Study type: Interventional

This is a randomized, controlled, open, three-armed, multi-centre study designed to compare the effects of dual-release hydrocortisone preparations versus conventional glucocorticoid therapy on anthropometric parameters, metabolic syndrome, infectious, immunological profile, cardiovascular system, bone mass and quality of life in patients affected by primary or secondary adrenal insufficiency.

NCT ID: NCT02273713 Completed - Esophageal Cancer Clinical Trials

The Addition of Nab-paclitaxel (Abraxane) to First Line Treatment of Metastasized Oesophagogastric Carcinoma (ACTION)

ACTION
Start date: October 2014
Phase: Phase 1/Phase 2
Study type: Interventional

Oesophagogastric cancer is a major cause of cancer related mortality, with an overall 5-year survival rate of 10% worldwide and patients are often diagnosed with locally advanced or metastasized disease at first presentation. For advanced oesophagogastric cancer fluoropyrimidines are the backbone of palliative chemotherapy and is commonly used in 2- or 3-drug combinations . However, in clinical practice after progression on first line therapy, a substantial number of oesophagogastric cancer patients may not be able to start second line chemotherapy due to rapid clinical deterioration. Therefore, new triplets with high anti-tumor activity and low toxicity are urgently needed. Given the activity of capecitabine and oxaliplatin containing regimens and the potential of taxanes in oesophagogastric cancer, the investigators propose a phase I study combining capecitabine and oxaliplatin with Nab-paclitaxel. Solvent-based taxanes (paclitaxel, docetaxel) can cause severe toxicities not only by the active agents itself but also by the solvents like cremophor. Nab-paclitaxel (Abraxane) is a solvent-free formulation of paclitaxel encapsulated in albumin. It does not require premedication with corticosteroids or antihistamines to prevent the risk of solvent-mediated hypersensitivity reactions. This new formulation improves safety profile, allows higher dosing with shorter infusion duration, and produces higher tumor drug concentration. It has proven activity in breast cancer, non small lung cancer and pancreatic cancer, as well as in gastric cancer models.

NCT ID: NCT02273570 Recruiting - Clinical trials for Hyperparathyroidism, Secondary

Optimal Anemia Treatment in End Stage Renal Disease (ERSD)

OPTIMAL
Start date: March 2015
Phase: N/A
Study type: Interventional

Clinical study aimed at improving anemia management in End Stage Renal Disease Patient (ESRD) on maintenance Hemodialysis with evidence of Chronic Kidney disease Mineral Bone Disorder (CKD-MBD)

NCT ID: NCT02265549 Completed - Clinical trials for Metastases, Neoplasm

Radiomics for Prediction of Long Term Survival and Local Failure After Stereotactic Radiotherapy for Brain Metastases

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

Published prognostic scores have limitations in prediction of long term survival after stereotactic radiotherapy for brain metastases. Moreover, no validated tools are available for prediction of local failure. The value of radiomics is evaluated in this perspective.

NCT ID: NCT02265536 Completed - Neoplasms Clinical Trials

A Study of LY3022855 In Participants With Breast or Prostate Cancer

Start date: May 2015
Phase: Phase 1
Study type: Interventional

The main purpose of this study is to learn more about how the investigational drug, LY3022855, affects the immune system in participants with advanced breast or prostate cancer that has not responded to other treatments. Treatment may last up to 6 cycles (cycle = 6 weeks).

NCT ID: NCT02260557 Completed - Clinical trials for Raynaud's Phenomenon Secondary to Systemic Sclerosis

Effects of Selexipag in Adults With Raynaud's Phenomenon Secondary to Systemic Sclerosis

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

The primary objective of the study is to determine the activity of selexipag on Raynaud attack frequency in subjects with Raynaud's Phenomenon (RP) secondary to Systemic Sclerosis (SSc).

NCT ID: NCT02260531 Completed - Breast Cancer Clinical Trials

Cabozantinib +/- Trastuzumab In Breast Cancer Patients w/ Brain Metastases

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

This research study is evaluating the effectiveness of the drug called cabozantinib (alone or in combination with trastuzumab) as a possible treatment for advanced breast cancer in which the cancer has spread to the brain.

NCT ID: NCT02251821 Active, not recruiting - Clinical trials for Primary Myelofibrosis

JAK Inhibitor Before Donor Stem Cell Transplant in Treating Patients With Primary or Secondary Myelofibrosis

Start date: October 20, 2014
Phase: Phase 2
Study type: Interventional

This phase II trial studies how well giving a JAK inhibitor before a donor stem cell transplant works in treating patients with myelofibrosis that developed without another condition (primary) or evolved from other bone marrow disorders (secondary). JAK inhibitors are a class of drugs that may stop the growth of abnormal cells by blocking an enzyme needed for cell growth. Giving a JAK inhibitor such as ruxolitinib before a donor stem cell transplant may help reduce symptoms of myelofibrosis such as inflammation and enlargement of the spleen, improve the patient's general physical condition, and prevent complications from occurring after the transplant. Infusing healthy stem cells from a donor into the patient may help the patient's bone marrow work normally and make stem cells, red blood cells, white blood cells, and platelets. Giving a JAK inhibitor before a donor stem cell transplant may help improve transplant outcomes in patients with myelofibrosis.