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NCT ID: NCT01427387 Completed - Healthy Clinical Trials

A Study to Evaluate Safety of Multiple Dose of ASP0456 in Healthy Subjects

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

A study to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of multiple ascending dose of ASP0456 in non-elderly healthy subjects. Two dosing condition, pre-prandial and postprandial administrations, is compared.

NCT ID: NCT01425723 Completed - Severe Hemophilia B Clinical Trials

Long-Term Safety and Efficacy of rFIXFc in the Prevention and Treatment of Bleeding Episodes in Previously Treated Participants With Hemophilia B

B-YOND
Start date: December 8, 2011
Phase: Phase 3
Study type: Interventional

The primary objective of the study is to evaluate the long-term safety of rFIXFc in participants with hemophilia B. The secondary objective of this study is to evaluate the efficacy of rFIXFc in the prevention and treatment of bleeding episodes.

NCT ID: NCT01425632 Completed - Clinical trials for Perennial Allergic Rhinitis

A Confirmatory Study of TAU-284 in Pediatric Patients With Perennial Allergic Rhinitis

Start date: August 2011
Phase: Phase 3
Study type: Interventional

The objectives of this study are: to confirm the superiority of TAU-284 over placebo after two weeks of administration to pediatric patients with perennial allergic rhinitis, and to investigate the dose response, safety, and plasma concentrations of TAU-284.

NCT ID: NCT01424319 Completed - Clinical trials for Chronic Kidney Disease

Reducing Residual Albuminuria in Subjects With Diabetes and Nephropathy With Atrasentan

Start date: August 2011
Phase: Phase 2
Study type: Interventional

Prospective, randomized, double-blind, placebo controlled, 12-week, multicenter study. The objective of the study is to evaluate the efficacy and safety of once daily administration of atrasentan tablets compared to placebo in reducing residual albuminuria in Japanese Type 2 diabetic patients with nephropathy who are treated with the maximum tolerated labeled dose for hypertension of a RAS (renin angiotensin system) inhibitor.

NCT ID: NCT01423994 Completed - Syncope Clinical Trials

Syncope: Pacing or Recording in the Later Years

Spritely
Start date: August 2011
Phase: Phase 4
Study type: Interventional

Syncope affects about 50% of Canadians, is the cause of 1 - 2% of all emergency room visits, and probably is responsible for CDN $250 million in health care spending each year. It is associated with decreased quality of life, trauma, loss of employment, and limitations in daily activities. It is a particular problem for older people, partly because of increased frailty, and partly because of a difficult differential diagnosis. One of the causes in older adults is intermittent complete heart block in the setting of bifascicular heart block, but they may also faint due to a variety of tachyarrhythmias, sick sinus syndrome, and several neurally mediated syncopes. Often treatment decisions should be made before the true cause is apparent.

NCT ID: NCT01423435 Completed - Healthy Adult Male Clinical Trials

Study to Compare Pharmacokinetic Profiles of TRK-100STP in Japanese, Chinese, and South Korean Non-elderly Healthy Adult Males

Start date: August 2011
Phase: Phase 1
Study type: Interventional

A study to evaluate the pharmacokinetics and safety of TRK-100STP in Japanese, Chinese, and South Korean non-elderly healthy adult males.

NCT ID: NCT01422434 Completed - Psoriasis Clinical Trials

LEO 90105 Ointment in Japanese Subjects With Psoriasis

Start date: July 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the efficacy of LEO 90105 ointment applied once daily with Dovonex® ointment applied twice daily and with Rinderon®-DP ointment applied once daily in Japanese subjects with psoriasis vulgaris.

NCT ID: NCT01422421 Completed - Hypertension Clinical Trials

Intensive Blood Pressure and LDL Lowering in Diabetic Patients With Coronary Artery Disease

Start date: August 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether intensive blood pressure and low density lipoprotein (LDL) cholesterol lowering could improve survival and cardiovascular outcome in Japanese diabetic patients with coronary artery disease and history of acute coronary syndrome.

NCT ID: NCT01421147 Completed - Clinical trials for Diabetes Mellitus, Type 1

A Study in Adults With Type 1 Diabetes

ELEMENT 1
Start date: August 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the effectiveness and safety of LY2963016 versus Lantus when taken once daily in combination with insulin lispro before meals three times a day.

NCT ID: NCT01420601 Completed - Clinical trials for Renal Cell Carcinoma

Temsirolimus (Torisel) Special Investigation (Regulatory Post Marketing Commitment Plan)

Start date: September 2011
Phase:
Study type: Observational

To confirm the safety of the long-term use of TORISEL 25 mg for Intravenous Drip Infusion particularly for the onset of interstitial lung disease from Weeks 25 to 96 after the start of administration.