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NCT ID: NCT02365441 Active, not recruiting - Clinical trials for Gastrointestinal Stromal Tumour

A Randomised Trial of Imatinib Alternating With Regorafenib Compared to Imatinib Alone for the First Line Treatment of Advanced Gastrointestinal Stromal Tumour (GIST)

ALT GIST
Start date: June 30, 2015
Phase: Phase 2
Study type: Interventional

An open label randomised trial for adults with histologically confirmed measurable metastatic GIST who have received no other treatment for metastatic disease. The study aims to determine if an alternating regimen of imatinib and regorafenib has sufficient activity and safety in comparison to imatinib alone to warrant further evaluation as a first line treatment for metastatic GIST.

NCT ID: NCT02362503 Active, not recruiting - HIV Infections Clinical Trials

Attachment Inhibitor Comparison in Heavily Treatment Experienced Patients

Start date: February 23, 2015
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether the BMS Attachment Inhibitor (BMS-663068) is effective in the treatment of heavily treatment experienced HIV-1 patients with multi-drug resistance.

NCT ID: NCT02360683 Active, not recruiting - Parkinson's Disease Clinical Trials

Predictive Factors and Subthalamic Stimulation in Parkinson's Disease

PREDI-STIM
Start date: November 18, 2013
Phase:
Study type: Observational

This study identify preoperative predictors of response to subthalamic stimulation at 1 year, 3 years and 5 years in terms of quality of life, from a broad prospective multicenter study French with standardized collection of clinical data , imaging and genetic . The investigators want to identify factors that predict the improvement of quality of life for one year corresponding to a decrease of PDQ39 score of at least 20 %. They believe that improvement would be less likely to become zero to 3 or 5 years and question the indication of the subthalamic stimulation (risks and costs). This is part of a process of "personalization" of the therapeutic care that is of any interest to the subthalamic stimulation. It is a therapeutic option that could be dangerous if patient selection is not optimal , and expensive, if the benefit is not large enough to reduce the number of medications and hospitalizations medium term . In addition, it will quantify the improvement of quality of life in the longer term and harmonize national assessments .

NCT ID: NCT02360579 Active, not recruiting - Metastatic Melanoma Clinical Trials

Study of Lifileucel (LN-144), Autologous Tumor Infiltrating Lymphocytes, in the Treatment of Patients With Metastatic Melanoma

LN-144
Start date: September 2015
Phase: Phase 2
Study type: Interventional

Prospective, interventional multicenter study evaluating adoptive cell therapy (ACT) via infusion of LN-144 (autologous TIL) followed by interleukin 2 (IL-2) after a nonmyeloablative lymphodepletion (NMA LD) preconditioning regimen.

NCT ID: NCT02360176 Active, not recruiting - Clinical trials for Surgical Treatment of Obesity

Benefit of Single Port-surgery in Sleeve Gastrectomy

MINIOB
Start date: January 4, 2017
Phase: N/A
Study type: Interventional

Demonstrate non-inferiority of the single port for sleeve gastrectomy compared to the reference method in terms of complications using a score of morbidity and mortality at 6 and 24 months: Rate of fistula, intra and extra abdominal abcess, hemorrhage, gastric stenosis, splenic lesions, hernia, residual gastric pouch and mortality

NCT ID: NCT02354079 Active, not recruiting - Clinical trials for Hypobetalipoproteinemia

HYPOCHOL : A Genetically-based Strategy to Identify New Targets in Cholesterol Metabolism

HYPOCHOL
Start date: January 7, 2016
Phase: N/A
Study type: Interventional

The aim of this study is to identify new targets in cholesterol metabolism thanks to a genetically-based strategy.

NCT ID: NCT02342158 Active, not recruiting - Neoplasm Metastasis Clinical Trials

Identifying Molecular Alterations to Guide Individualized Treatment in Advanced Solid Tumors

PERMED01
Start date: November 12, 2014
Phase: N/A
Study type: Interventional

PERMED01 is a prospective monocenter clinical trial which aims to evaluate the number patients with locally advanced or metastatic cancer for whom identification of molecular alterations in tumor samples can lead to the delivery of a targeted therapy. PERMED01 will enroll 460 patients in 3 years.

NCT ID: NCT02339532 Active, not recruiting - Breast Cancer Clinical Trials

Neoadjuvant Phase II Trial in Patients With T1c Operable, HER2-positive Breast Cancer According to TOP2A Status

NeoTOP
Start date: January 2015
Phase: Phase 2
Study type: Interventional

The main objective of this multicenter study will therefore be to evaluate pathologic complete response rates of an anthracycline-based regimen [FEC 100 - TAXOTERE® - HERCEPTIN® - PERTUZUMAB] and a non anthracycline-based regimen [TAXOTERE® - CARBOPLATINE - HERCEPTIN® - PERTUZUMAB] according to the presence or not of TOP2A gene amplification in a population of breast cancer patients with HER2 overexpression. A very important objective of the study will be the evaluation of biomarkers that predict response to treatment.

NCT ID: NCT02337244 Active, not recruiting - Clinical trials for Rheumatoid Arthritis

Zimmer POLAR Persona - TKA (EMEA Study)

Start date: November 18, 2013
Phase:
Study type: Observational

The primary objective of this study is to obtain implant survivorship and clinical outcomes data for commercially available Persona knee implants used in primary total knee arthroplasty. The assessment will include: 1. Implant survivorship based on removal of a study device. 2. Safety based on incidence and frequency of adverse events. 3. Clinical performance measured by overall pain and function, quality of life data, radiographic parameters and survivorship.

NCT ID: NCT02333838 Active, not recruiting - Leukemia, Myeloid Clinical Trials

Reduced Toxicity Conditioning Prior to Unrelated Cord Cell Transplantation for High Risk Myeloid Malignancies

TBF-Cord
Start date: May 2015
Phase: Phase 2
Study type: Interventional

Allogeneic cord blood stem cell transplantation is a potentially curative therapy for patients with haematological malignancies. We have extensive experience with the use of Cord Blood Transplantation (CBT) in patients with advanced myeloid malignancies. In adults however, the 40% Non-Relapse Mortality (NRM) rate observed after CBT conditioned with a myeloablative conditioning has encouraged the development of CBT with Reduced Intensity Conditioning (RIC). Our previous national CBT protocol (the Minicord French protocol - NCT00797758) showed that RIC CBT can reduce NRM, but relapse remains the main post-transplant event (>30% at one year). Thus, the development of reduced toxicity rather than RIC conditioning for CBT is warranted in order to improve the outcome of such transplants by limiting NRM and reducing relapse rate. The Fludarabine, ATG and intensified doses of IV Busulfan (9.6 mg/Kg total dose) regimen is a well-established preparative regimen for reduced-intensity/toxicity conditioning prior to allogeneic stem cell transplantation using peripheral blood stem cells mobilized with G-CSF (ClinicalTrials.gov Identifier: NCT00841724). However, such regimen is likely not sufficient to allow for CB cell engraftment. Thiotepa is an alkylating and radio-mimetic agent with a large anti-tumor activity including leukemic cells, the ability to cross the blood-brain barrier and to improve engraftment of hematopoietic stem cells. This drug has been combined to usual conditioning regimen without increasing the toxicity but improving the engraftment rate and potentially reducing the relapse rate. Thus, in the context of adult CBT for high risk myeloid malignancies, we propose to prospectively evaluate a reduced toxicity conditioning based on the association of Thiotepa, Fludarabine, IV Busulfan and ATG with the objective to achieve acceptable NRM rates, and to allow for improved anti-leukemic control based on the cytotoxic component of the conditioning regimen itself, while waiting for the long term immune-mediated disease control (GVL effect).