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Neoplasms clinical trials

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NCT ID: NCT01785810 Completed - Clinical trials for Hematologic Malignancy

Phase II Maraviroc for GVHD Prevention

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

RATIONALE: Successful allogeneic stem-cell transplantation is often limited by graft-versus-host disease (GVHD). Migration of donor cells into tissues plays a major role in GVHD. Drugs that block chemokine receptors such as CCR5, can potentially decrease the migration of donor cells into tissues. Blocking CCR5 after allogeneic stem-cell transplantation may therefore reduce the rates of GVHD. PURPOSE: This study explores the efficacy of pharmacologic inhibition of CCR5 in prevention of GVHDby administering maraviroc during allogeneic stem-cell transplantation with reduced intensity conditioning.

NCT ID: NCT01781455 Completed - Clinical trials for Cancer, Advanced Solid Tumors

A Study of BBI503 in Adult Patients With Advanced Solid Tumors

Start date: February 2012
Phase: Phase 1
Study type: Interventional

This is an open label, single arm dose escalation study of BBI503 in adult patients with advanced solid tumors.

NCT ID: NCT01781429 Completed - Clinical trials for Advanced Solid Tumors

Phase I Dose-Escalation, Safety, Pharmacokinetic and Pharmacodynamic Study of BVD-523 in Patients With Advanced Malignancies

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

This open-label, multi-center Phase 1/2 study will assess the safety, pharmacokinetics, and pharmacodynamics of escalating doses of BVD-523 in patients with advanced malignancies. The study also seeks to demonstrate target modulation and early signs of clinical response in select patient populations.

NCT ID: NCT01779882 Completed - Myeloid Leukemia Clinical Trials

Cyclophosphamide and Busulfan as Conditioning Regimen Before Allogeneic HSCT

Start date: January 2013
Phase: N/A
Study type: Interventional

The aim of this study is to test the hypothesis, that the order of application of Busulfan (BU) and Cyclophosphamide (CY) has an impact on toxicity after allogeneic Hematopoietic stem cell transplantation (HSCT) and that CY-BU reduces liver toxicity compared to BU-CY.

NCT ID: NCT01778920 Completed - Neoplasms Clinical Trials

Pilot and Feasibility Study of the Imaging Potential of EC17: Intraoperative Folate-fluorescein Conjugate (EC17) Lung Cancer (CA)

Start date: April 2012
Phase: Phase 1
Study type: Interventional

The goal of this study is to perform imaging of patient's tumors while the chest is open and the tumor is being removed. According to the World Health Organization, lung cancer is the most common cause of cancer-related death in men and women, and is responsible for 1.3 million deaths worldwide annually as of 2004. Surgery remains the best option for patients presenting with operable Stage I or II cancers, however the five year survival rate for these candidates remains at a dismal 53% for Stage I and 32% for Stage II. The high rates of recurrence suggest that surgeons are unable to completely detect and remove primary tumor nodules in a satisfactory manner as well as lingering metastases in sentinel lymph nodes. By ensuring a negative margin through imaging during surgery it would be possible for us to improve the rates of recurrence free patients and thus overall survival. Thoracic malignancies are the ideal disease to investigate intra-operative imaging. Over 85% of lung and pleural malignancies express folate receptor alpha (FRA). It is important to note that FRA is expressed only in the proximal tubules of the kidneys, activated macrophages, and in the choroidal plexus. Thus, the false positive detection rate is expected to be extremely low. A group well known to us in the Netherlands has completed a pilot study utilizing a folate-fluorescein isothiocyanate (folate-FITC) conjugate in 12 patients with ovarian cancer. Another group of investigators in Mayo have subsequently performed this study on 20 more patients without any serious adverse events (personal communication). They report excellent sensitivity and specificity with this technique with only grade 1 side effects (allergic reaction). All side effects reversed when the injection was halted. Patients with a history of allergic reactions to insect bites should not participate (fluorescein is derived from the firefly insect, folate is an essential vitamin).

NCT ID: NCT01778439 Completed - Clinical trials for Relapsed or Refractory Solid Tumors

A Dose Escalation Study of OMP-52M51 in Subjects With Solid Tumors

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

This is an open-label Phase 1a dose escalation study of single-agent OMP-52M51 in subjects with relapsed or refractory solid tumors. Study includes a dose escalation phase and expansion phase. Subjects will be assessed for safety, immunogenicity, pharmacokinetics, biomarkers, and efficacy.

NCT ID: NCT01776385 Completed - Mesothelioma Clinical Trials

The ISET (Isolation by Size of Epithelial Tumor Cells) and the CellSearch Methods in Malignant Pleural Mesothelioma

Start date: February 2012
Phase: N/A
Study type: Interventional

Malignant pleural mesothelioma (MPM) has a growing incidence and in spite of early diagnostic, their outcome remains dismal. The evolution of MPM is often local with rare distant metastases. There is now a sizable body of evidence that metastases could develop from circulating tumor cells (CTC) spread in blood before or during surgery. Thus, sensitive and specific detection of CTC in blood is considered as a potentially relevant predictive biomarker for patients with carcinomas. In exchange, the prognostic value of CTC in MPM has not yet been evaluated. Indeed, the main goal for preoperative detection of CTC is to identify patients with high risk of recurrence after surgery, in order to perform more adapted therapeutic strategy. Despite several studies reported about CTC detection, methodological aspects concerning sensitivity, specificity and reproducibility have prevented a clear appraisal of their clinical impact. Thus, the aim of our study is to evaluate the presence and the prognostic value of CTC in MPM by a double approach. In our setting, cytopathological analysis of circulating non hematological cells (CNHC), of epithelial origin, isolated according to their size (ISET, Isolation by Size of Epithelial Tumor cells) along with immunomagnetic selection, identification and enumeration of circulating epithelial cells in peripheral blood (CellSearch method) is considered a promising approach.

NCT ID: NCT01775631 Completed - B-Cell Malignancies Clinical Trials

Combination Study of Urelumab and Rituximab in Patients With B-cell Non-Hodgkins Lymphoma

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

The purpose of the study is to determine the safety, tolerability and maximum tolerated dose of Urelumab in combination with Rituximab in patients with B-cell Non-Hodgkins Lymphoma

NCT ID: NCT01775423 Completed - Clinical trials for Cancer, Advanced Malignancies

A Study of BBI608 in Adult Patients With Advanced Malignancies

Start date: March 2009
Phase: Phase 1
Study type: Interventional

This is an open label, single arm, dose escalation study of BBI608 in patients with advanced malignancies.

NCT ID: NCT01773421 Completed - Clinical trials for Advanced Solid Tumors

An Open-label, Dose Escalation, Pharmacodynamic, Pharmacokinetic, and Effect of Food Phase 1 Study of E7820 to Determine the Maximum Tolerated Dose Following Twice Daily Oral Administration in Subjects With Unresectable Solid Tumors

Start date: June 30, 2011
Phase: Phase 1
Study type: Interventional

This study consists of two Parts. Part A (Food Effect Study) and Part B (Determination of Maximum Tolerated Dose [MTD] for twice daily [BID] Dosing).Part A will be initiated first, and Part B will be initiated after the PK results of Part A have been evaluated.