Clinical Trials Logo

Filter by:
NCT ID: NCT01617460 Completed - Autistic Disorder Clinical Trials

A Long-term, Extended Treatment Study of Aripiprazole in Pediatric Patients With Autistic Disorder

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

The objective of this study is to investigate the safety and efficacy of aripiprazole orally administered over long term in subjects who complete a short-term treatment study of pediatric Autistic Disorder (031-11-002 study).

NCT ID: NCT01617447 Completed - Autistic Disorder Clinical Trials

A Short Treatment Study of Aripiprazole in Pediatric Patients With Autistic Disorder

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

The objective of this study is to investigate the efficacy and safety of aripiprazole orally administered over a period of 8 weeks in pediatric patients with Autistic Disorder

NCT ID: NCT01616524 Completed - Clinical trials for Hepatitis C Virus (HCV)

Safety and Efficacy Study of Pegylated Interferon Lambda With and Without Daclatasvir, Compared to Pegylated Interferon Alfa, Plus Ribavirin in Subjects With Hepatitis C Genotype 2 and 3

PRINCIPAL
Start date: July 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if 24 weeks of treatment with Pegylated Interferon Lambda plus Ribavirin and 12 weeks of treatment with Pegylated Interferon Lambda plus Ribavirin and Daclatasvir will be safe and effective for treatment of hepatitis C compared to 24 weeks of treatment with Pegylated Interferon Alfa-2a plus Ribavirin

NCT ID: NCT01615978 Completed - Clinical trials for Diabetes Mellitus, Type 2

Safety and Tolerability of Liraglutide in Japanese Subjects With Type 2 Diabetes

Start date: December 2003
Phase: Phase 1
Study type: Interventional

This trial is conducted in Japan. The aim of this trial is to assess the safety after multiple s.c. (subcutaneously) doses of liraglutide in Japanese subjects with type 2 diabetes.

NCT ID: NCT01615198 Completed - Clinical trials for Essential Hypertension

Efficacy and Safety of LCZ696 in Comparison to Olmesartan in Elderly Patients With Essential Hypertension

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

The purpose of this study is to access the efficacy and safety of LCZ696 compared to olmesartan in elderly Asian patients for the treatment of hypertension.

NCT ID: NCT01614912 Completed - Schizophrenia Clinical Trials

Long-term Extension Study of SM-13496 (Lurasidone HCl) in Patients With Schizophrenia

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

The study evaluates the long term safety and efficacy of SM-13496 in patients with schizophrenia.

NCT ID: NCT01614899 Completed - Schizophrenia Clinical Trials

A Phase III Study of SM-13496 (Lurasidone HCl) in Patients With Schizophrenia

Start date: July 2, 2012
Phase: Phase 3
Study type: Interventional

The study evaluates the efficacy and safety of SM-13496 compared with placebo in patients with schizophrenia.

NCT ID: NCT01614886 Completed - Alzheimer's Disease Clinical Trials

Randomized, Double-blind Study to Evaluate the Tolerability of 2 Different Titration Methods of Rivastigmine Patch in AD Patients (MMSE 10-20)

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

To evaluate the tolerability, safety and efficacy of 3-step titration versus 1-step titration of Rivastigmine patch in the Japanese population.

NCT ID: NCT01614574 Completed - Gaucher Disease Clinical Trials

Study of Velaglucerase Alfa Enzyme Replacement Therapy in Japanese Patients With Gaucher Disease

Start date: March 2, 2012
Phase: Phase 3
Study type: Interventional

Gaucher disease is an inherited deficiency of the lysosomal enzyme glucocerebrosidase (GCB) that leads to progressive accumulation of glucocerebroside within macrophages and subsequent tissue and organ damage; typically of the liver, spleen, bone marrow, and brain. The disease has been classified into 3 clinical subtypes based on the presence or absence of neurological symptoms and severity of neurological disease. Type 1 Gaucher disease affects an estimated 30,000 persons worldwide and is the most common. Type 1 Gaucher disease does not involve the central nervous system. Patients with type 2 Gaucher disease present with acute neurological deterioration, which leads to early death. Those with type 3 disease typically display a more sub-acute neurological course, with later onset and slower progression. The primary objective of this study is to evaluate the safety of every other week dosing of velaglucerase alfa in Japanese patients with Gaucher disease. Velaglucerase alfa has been developed and approved as an enzyme replacement therapy for Type 1 Gaucher disease.

NCT ID: NCT01613976 Completed - Clinical trials for Acute Myeloid Leukemia (AML)

A Phase Ib Study of Panobinostat (LBH589) in Combination With 5-Azacitidine for Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukemia (CMML) or Acute Myeloid Leukemia (AML) Patients

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

The purpose of this study is to confirm the safety and tolerability of oral panobinostat (PAN) in combination with a fixed dose of 5-Azacitidine (5-Aza) in adult Japanese patients with Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukemia (CMML) or Acute Myeloid Leukemia (AML).