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NCT ID: NCT00264433 Completed - Neoplasms Clinical Trials

A Study of the Safety and Effects of ADH-1 Given Intravenously as a Single Agent

Start date: n/a
Phase: Phase 2
Study type: Interventional

N-cadherin, a protein involved in blood vessel cell binding, is increased as cancer progresses, and is on the surface of many tumor cells. ADH-1 blocks N-cadherin. This study will test the safety and effects of ADH-1 in subjects with specific incurable, solid tumors with a protein biomarker called N-cadherin. This study will examine the clinical activity of ADH-1.

NCT ID: NCT00264446 Completed - Neoplasms Clinical Trials

A Study of ADH300004 in Surgically Resected Primary or Metastatic Colorectal Cancer and Liver Biopsy, or Planned Hepatic Resection

Start date: n/a
Phase: Phase 1
Study type: Interventional

5 fluorouracil (5 FU), one of the most actively investigated anti-cancer drugs, is rapidly inactivated by the enzyme dihydropyrimidine dehydrogenase (DPD). ADH300004 blocks DPD. This study will examine the kinetics of inhibition and recovery of the metabolic pathways for fluoropyrimidines in subjects who receive a single oral dose of ADH300004, and may allow optimization of oral 5 FU dosing to subjects in future studies.

NCT ID: NCT00265499 Completed - Clinical trials for Coronary Artery Disease

The Internal Thoracic Artery Skeletonization Study: A Paired, Within-Patient Comparison

Start date: n/a
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether skeletonization of the internal thoracic artery leads to improved flow, increased length, improved sternal perfusion, and decreased pain and dysesthesia in patients undergoing coronary artery bypass surgery

NCT ID: NCT00266552 Completed - Conduct Disorder Clinical Trials

A Study of the Safety and Effectiveness of Risperidone Versus Placebo for the Treatment of Conduct Disorder in Children With Mild, Moderate, or Borderline Mental Retardation

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of the study is to assess the effectiveness and safety of an oral solution of risperidone (an antipsychotic medication) versus placebo in the treatment of conduct disorder in children with mild, moderate, or borderline mental retardation.

NCT ID: NCT00266617 Completed - Neoplasms Clinical Trials

A Study to Evaluate the Safety and Effectiveness of Epoetin Alfa in Patients With Anemia as a Result of Advanced Cancer and Treatment With Aggressive Chemotherapy

Start date: n/a
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of epoetin alfa in the treatment of persistent anemia caused by advanced cancer and aggressive adriamycin-chemotherapy. Epoetin alfa is a genetically engineered protein that stimulates red blood cell production.

NCT ID: NCT00268866 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Danish Quality Assurance Project on Diagnosis and Treatment of Chronic Obstructive Pulmonary Disease (COPD) in Outpatient Lung Clinics

Start date: n/a
Phase: Phase 4
Study type: Observational

Danish Quality Assurance Project on Diagnosis and Treatment of COPD in Outpatient Lung Clinics

NCT ID: NCT00269464 Completed - Schizophrenia Clinical Trials

Chronic Schizophrenia With Obsessive-Compulsive Symptoms: Comorbidity or a Subtype?

Start date: n/a
Phase: N/A
Study type: Observational

Evaluating the prevalence and characteristics of obsessive-compulsive (OC) symptoms in patients with chronic schizophrenia

NCT ID: NCT00269802 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

A Multicenter Study Comparing the Efficacy and Safety of OROS Methylphenidate HCl, Ritalin (Methylphenidate HCl) and Placebo in Children With Attention Deficit Hyperactivity Disorder

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of OROS® Methylphenidate HCl as compared with placebo and standard immediate-release Ritalin® (taken three time per day) for the treatment of Attention Deficit Hyperactivity Disorder in children. Both OROS® Methylphenidate HCl and Ritalin® contain the central nervous system stimulant, methylphenidate HCl.

NCT ID: NCT00269815 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

Long-term Safety and Effectiveness of OROS Methylphenidate HCl in Children With Attention Deficit Hyperactivity Disorder

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the long-term safety and effectiveness of OROS® Methylphenidate HCl (a central nervous system stimulant) in children with attention deficit hyperactivity disorder (ADHD).

NCT ID: NCT00269945 Completed - Anemia Clinical Trials

A Study to Evaluate the Safety and Effectiveness of Epoetin Alfa in AIDS Patients With Anemia Caused Both by Their Disease and by AZT (Zidovudine, an Antiviral Drug) Given as Treatment for Their Disease

Start date: n/a
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effectiveness and safety of epoetin alfa versus placebo for the treatment of anemia in AIDS (Acquired Immunodeficiency Syndrome) patients with anemia that is a result of this disease and zidovudine (AZT) treatment. Epoetin alfa is a genetically engineered protein that stimulates red blood cell production.