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NCT ID: NCT01593787 Completed - Clinical trials for Hypertension With Renal Dysfunction

Safety and Tolerability and Efficacy of LCZ696 in Japanese Hypertensive Patients With Renal Dysfunction

Start date: May 2012
Phase: Phase 3
Study type: Interventional

This study assessed the safety, tolerability, and efficacy of LCZ696 in hypertensive patients with renal dysfunction.

NCT ID: NCT01588626 Completed - Healthy Clinical Trials

Study to Assess the Pharmacokinetics of AZD6140 After Single Dose in Healthy Japanese Male Volunteers

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

The purpose of this study is to assess the pharmacokinetics of AZD6140 and its active metabolite, safety, tolerability of AZD6140 following single administration in healthy male Japanese volunteers.

NCT ID: NCT01588548 Completed - Clinical trials for Advanced Solid Malignancies

Global Phase1 Study to Assess the Safety and Tolerability of AZD1208 in Advanced Solid Tumors and Malignant Lymphoma

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

The purpose of this study is to investigate the safety and tolerability of AZD 1208 up to a maximum tolerated dose (MTD) and define the dose(s) for further clinical evaluation when given daily to patients with advanced solid malignancies including malignant lymphoma

NCT ID: NCT01588353 Completed - Clinical trials for Dupuytren's Contracture

Collagenase Option for Reduction of Dupuytren's Contracture in Japan

CORD-J
Start date: May 2012
Phase: Phase 3
Study type: Interventional

To investigate the efficacy and safety of AK160 in patients with Dupuytren's Contracture. To determine plasma concentration after the first injection of AK160 in patients with Dupuytren's Contracture.

NCT ID: NCT01586936 Completed - Clinical trials for Congenital Bleeding Disorder

Non-Interventional Study of NovoSeven® Used as On-demand Treatment of Bleeds in Patients With Haemophilia A and B With Inhibitors

Start date: March 10, 1999
Phase: N/A
Study type: Observational

This study is conducted in Japan. The aim of this registry study is to observe the use of single dose and multi-dose use of eptacog alpha (NovoSeven®) and to compare short-term outcomes, including effectiveness, safety, quality of life and treatment satisfaction with the approved treatments.

NCT ID: NCT01585987 Completed - Clinical trials for Locally Advanced (Unresectable) or Metastatic Adenocarcinoma of the Gastric and Gastro-esophageal Junction

An Efficacy Study in Gastric and Gastroesophageal Junction Cancer Comparing Ipilimumab Versus Standard of Care Immediately Following First Line Chemotherapy

Start date: July 2012
Phase: Phase 2
Study type: Interventional

The purpose of the study is to compare the efficacy of Ipilimumab and standard of care as sequential or maintenance treatment immediately after first-line chemotherapy in the treatment of unresectable or metastatic gastric and gastro-esophageal cancer.

NCT ID: NCT01585792 Completed - Diabetic Patients Clinical Trials

Double Blind Comparative Study of TAK-875

Start date: May 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of treatment with TAK-875 in diabetic patients.

NCT ID: NCT01585155 Completed - Clinical trials for Pediatric Ulcerative Colitis

Clinical Study of TA-650 in Pediatric Patients With Ulcerative Colitis

Start date: February 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the the efficacy of TA-650 using Clinical activity index (CAI) score and other evaluation indicators in pediatric patients with moderate to severe ulcerative colitis after TA-650 administration of at a dose of 5 mg/kg at weeks 0, 2, and 6, and then every 8 weeks at weeks 14 and 22. The safety and pharmacokinetics are also evaluated.

NCT ID: NCT01584843 Completed - Strabismus Clinical Trials

Efficacy and Safety of GSK1358820 (Botulinum Toxin Type A) in Patients With Strabismus

Start date: May 2012
Phase: Phase 3
Study type: Interventional

Primary objective is to evaluate the efficacy of single-dose treatment with GSK1358820 compared with non-treatment in patients with strabismus based on angles of strabismus in the primary position.

NCT ID: NCT01584232 Completed - Clinical trials for Type 2 Diabetes Mellitus

A Study of Dulaglutide in Japanese Participants With Type 2 Diabetes Mellitus

Start date: April 2012
Phase: Phase 3
Study type: Interventional

The purpose of this trial is to examine the efficacy and safety of once-weekly LY2189265 (dulaglutide) in participants with type 2 diabetes mellitus taking an oral antihyperglycemic medication (OAM).