Clinical Trials in Austin

Showing 11001-11020 of 13,060 trials

VEC-162 Study in Healthy Adult Volunteers in a Model of Insomnia

NCT00291187

The purpose of this study is to determine the safety and efficacy of VEC-162 compared to placebo to improve sleep parameters in a model of insomnia.

Insomnia

Vanda Pharmaceuticals411 participantsStarted Feb 2006

Birmingham, Alabama, United States • Phoenix, Arizona, United States • San Diego, California, United States +16 more locations

COMPLETEDPhase 3< 1 mile

VEC-162 Study in Adult Patients With Primary Insomnia

NCT00548340

The purpose of this study is to evaluate the efficacy and safety of a 5 week double-blind treatment period of VEC-162 as compared to placebo in male and female patients with primary insomnia.

Primary Insomnia

Vanda Pharmaceuticals322 participantsStarted Nov 2007

Birmingham, Alabama, United States • Hot Springs, Arkansas, United States • Little Rock, Arkansas, United States +32 more locations

VEC-162 Study in Healthy Adult Volunteers in a Model of Insomnia

VEC-162 Study in Adult Patients With Primary Insomnia

Find Trials by Condition in Austin

Efficacy & Safety of Inhaled Insulin in Type 1 Diabetes

To Compare Treatment With Doxorubicin or Capecitabine for Metastatic Breast Cancer in Women 60 Years and Older

Ranolazine Monotherapy in Subjects With Type 2 Diabetes Mellitus

Evaluating Cerebrospinal Fluid Biomarkers in Alzheimer's, Progressive Supranuclear Palsy Subjects, and Controls

A Dose Escalation Study of Iniparib as a Single Agent and in Combination in Solid Tumors

Efficacy and Safety in Subjects With Type 2 Diabetes Receiving Subcutaneous Basal Insulin and Prandial Inhalation of Technosphere/Insulin Versus Subcutaneous Premixed Insulin Therapy Over a 52-Week Treatment Period and a 4-Week Follow-up

A Multicenter Study to Evaluate the Effects of a 91-day Oral Contraceptive on Bone Mineral Density in Adolescent Females

Open-Label Phase III Long-Term Safety Trial of Liprotamase

Efficacy and Safety of Tasimelteon Compared With Placebo in Totally Blind Subjects With Non-24-Hour Sleep-Wake Disorder

Withdrawal Study to Demonstrate the Maintenance Effect in the Treatment of Non-24-Hour Sleep-Wake Disorder

Safety and Efficacy of Technosphere® Insulin Inhalation Powder and Lantus® Compared to Humalog® and Lantus® Over 16-Weeks

When to Start Anti-HIV Drugs in Patients With Opportunistic Infections

Study of SGN-40, Lenalidomide, and Dexamethasone in Patients With Multiple Myeloma

Efficacy and Safety of 2 Doses of Tiotropium Respimat Compared to Placebo in Adolescents With Severe Persistent Asthma

A Study of Ramucirumab in Participants With Gastric, Esophageal, and Gastroesophageal Cancer

Liprotamase Efficacy Trial in Patients With Cystic Fibrosis-Related Exocrine Pancreatic Insufficiency

Efficacy And Safety Of Clopidogrel In Neonates /Infants With Systemic To Pulmonary Artery Shunt Palliation

Assessing the Pharmacokinetics of NKTR-118 in Subjects With Renal Impairment Compared to That in Subjects With Normal Renal Function