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NCT ID: NCT00355472 Completed - Clinical trials for Adult T-Cell Leukemia and Lymphoma (ATL)

Phase I Study of KW-0761 in Relapsed Patients With CCR4-Positive ATL and PTCL

Start date: February 2007
Phase: Phase 1
Study type: Interventional

This is a Phase I label dose escalation study of KW-0761 in relapsed patients with CCR4 positive Adult T-Cell Leukemia-Lymphoma (ATL) and Peripheral T-Cell lymphoma (PTCL).

NCT ID: NCT00353028 Completed - Clinical trials for Major Depressive Disorder

Fluvoxamine Maleate in the Treatment of Depression/Depressive State : A Post-marketing Clinical Study in Children and Adolescents

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

This study is to verify the efficacy of fluvoxamine maleate given for 8 weeks in the treatment of children and adolescents with depression or depressive state

NCT ID: NCT00352768 Terminated - Clinical trials for Obsessive Compulsive Disorder

Fluvoxamine Maleate in the Treatment of Obsessive-Compulsive Disorder: A Post-marketing Clinical Study in Children and Adolescents

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

This study is to verify the efficacy of fluvoxamine maleate given for 10 weeks in treatment of children and adolescents with obsessive-compulsive disorder

NCT ID: NCT00351832 Completed - Clinical trials for Diabetes Mellitus, Type 2

A Study To Compare the Effect of Vildagliptin Compared to Placebo in Patients With Type 2 Diabetes

Start date: June 2006
Phase: Phase 3
Study type: Interventional

This study is not being conducted in the United States. Vildagliptin is an oral antidiabetic agent. This 12-week clinical study is to evaluate the effect of vildagliptin 50mg qd, 50mg bid or 100mg qd compared to placebo in patients with type 2 diabetes.

NCT ID: NCT00349180 Completed - Clinical trials for Arthroplasty, Replacement, Hip

Total Hip Replacement Study With XRP4563 (Enoxaparin Sodium)

Start date: June 2006
Phase: Phase 3
Study type: Interventional

This study is performed to confirm the optimal dose for THR (total hip replacement).

NCT ID: NCT00348309 Completed - Alzheimer's Disease Clinical Trials

Rosiglitazone (Extended Release Tablets) As Adjunctive Therapy For Subjects With Mild To Moderate Alzheimer's Disease

REFLECT-2
Start date: July 6, 2006
Phase: N/A
Study type: Interventional

Rosiglitazone (RSG) has been tested in clinical studies and is approved by the FDA as a treatment for type II diabetes mellitus, a disease that occurs when the body is unable to effectively use glucose. RSG XR, the investigational drug used in this study, is an extended-release form of RSG. This study tests whether RSG XR safely provides clinical benefit to people with mild to moderate Alzheimer's disease (AD) when combined with the currently approved AD medication, Aricept (donepezil). RSG XR is a new approach to AD therapy and this study tests a new way to treat AD by testing whether one's genetic makeup affects their response to the study drug. Clinical data suggesting that RSG may benefit AD patients was first seen in a small study performed at the University of Washington and then from a larger GSK study conducted in Europe and New Zealand. In the first study, subjects receiving RSG once daily for 6 months scored significantly better on 3 tests of memory and thought than those who did not receive RSG. In the GSK study, those that appeared to benefit most from treatment with RSG XR had a specific genetic pattern. They did not have the gene that caused them to produce the protein apolipoprotein E e4 (APOE e4). Subjects who have the APOE e4 gene may have two copies, one from each parent, or they may have only one APOE e4 gene meaning that they inherited either the APOE e2 or APOE e3 version of the gene, instead of APOE e4, from one of their parents. Subjects with one copy of the APOE e4 gene remained at their same level of thinking ability while those with two copies of the APOE e4 gene, continued to worsen during the 6-month treatment. The current study will more directly test the effectiveness or RSG XR on people who either have or lack the APOE e4 gene.

NCT ID: NCT00348296 Completed - Clinical trials for Scleroderma, Systemic

Efficacy and Safety Study of GB-0998 for Treatment of Systemic Sclerosis

Start date: July 2006
Phase: Phase 3
Study type: Interventional

This randomized, double-blind, placebo-controlled multi-center study will carry out to assess the efficacy of GB-0998 in the treatment of the systemic sclerosis based on the changes in modified Rodnan total skin thickness score (TSS) as primary endopoint, and in addition, to assess the safety of GB-0998.

NCT ID: NCT00348231 Recruiting - Clinical trials for Diabetes Mellitus, Type 2

Jikei Optimal Insulin Therapy in Type 2 Diabetes

Start date: November 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to compare whether there is the difference in the effect of insulin therapy by the number of times of insulin injection.

NCT ID: NCT00347061 Completed - Clinical trials for Benign Prostatic Hyperplasia

Long Term Safety of SL77.0499-10 (Alfuzosin) in Patients With BPH

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

Primary: To assess the safety of SL77.0499-10 10mg administered once daily for one year in patients with lower urinary tract symptoms related to BPH. Secondary: - To provide the information on the efficacy of SL77.0499-10 10mg administered once daily for one year in patients with lower urinary tract symptoms related to BPH. - To document the plasma concentration of SL77.0499-10 after repeated administration of SL77.0499-10 10mg administered once daily in patients with lower urinary tract symptoms related to BPH.

NCT ID: NCT00347048 Completed - Ulcerative Colitis Clinical Trials

Tacrolimus (FK506) Study in Moderate to Severe Refractory Ulcerative Colitis Patients

Start date: September 2006
Phase: Phase 3
Study type: Interventional

This study consists of a 2-week placebo-controlled double-blind inter-group efficacy study in moderate to severe refractory ulcerative colitis (UC) patients followed by a maximum of 12-week open-label efficacy and safety study in responders.