Wake Forest Baptist Health, Winston-Salem, North Carolina, United States
Wake Forest Baptist Health, Winston-Salem, North Carolina, United States
A Drug Interaction Study of VI-0521 With Metformin, Sitagliptan and Probenecid in Healthy Subjects.
Completed
No Results Available
Obesity
Obesity
Drug: Metformin, VI-0521, Sitagliptan, Probenecid
Drug: Metformin, VI-0521, Sitagliptan, Probenecid
MDS Pharma Services, Phoenix, Arizona, United States
MDS Pharma Services, Phoenix, Arizona, United States
A Study Comparing Multiple Doses of VI-0521 With Placebo and Their Single-agent Constituents for Treatment of Obesity in Adults
Completed
Has Results
Obesity
Obesity
Drug: VI-0521|Drug: topiramate|Drug: phentermine
Drug: VI-0521 Drug: topiramate Drug: phentermine
Research Site, Durham, North Carolina, United States|Research Site, Philadelphia, Pennsylvania, United States
Research Site, Durham, North Carolina, United States Research Site, Philadelphia, Pennsylvania, United States
A Toolbox Approach to Obesity Treatment in Primary Care
Completed
Has Results
Obesity
Obesity
Behavioral: Commercial weight loss program|Behavioral: Colorado Weigh|Dietary Supplement: Meal replacements|Drug: Obesity pharmacotherapy|Behavioral: Recreation center passes
Behavioral: Commercial weight loss program Behavioral: Colorado Weigh Dietary Supplement: Meal replacements Drug: Obesity pharmacotherapy Behavioral: Recreation center passes
Denver Health and Hospital Authority, Denver, Colorado, United States
Denver Health and Hospital Authority, Denver, Colorado, United States
A Study to Evaluate the Pharmacokinetics of VI-0521 Subjects With Renal Impairment
Completed
No Results Available
Renal Impairment
Renal Impairment
Drug: Topirmate and Phentermine
Drug: Topirmate and Phentermine
Advanced Clinical Research Institute, Anaheim, California, United States|Clinical Pharmacology of Miami, Miami, Florida, United States|Orlando Clinical Research Center, Orlando, Florida, United States|DaVita Clinical Research, Minneapolis, Minnesota, United States
Advanced Clinical Research Institute, Anaheim, California, United States Clinical Pharmacology of Miami, Miami, Florida, United States Orlando Clinical Research Center, Orlando, Florida, United States DaVita Clinical Research, Minneapolis, Minnesota, United States
A Study to Evaluate the Pharmacokinetics of VI-0521 in Subjects With Hepatic Impairment
Completed
No Results Available
Hepatic Impairment
Hepatic Impairment
Drug: Phentermine and Topiramate
Drug: Phentermine and Topiramate
Clinical Pharmacology of Miami, Miami, Florida, United States|Orlando Clinical Research Center, Orlando, Florida, United States
Clinical Pharmacology of Miami, Miami, Florida, United States Orlando Clinical Research Center, Orlando, Florida, United States
Effect of VI-0521 (Qsymia®) on Glomerular Filtration Rate (GFR) in Overweight or Obese Healthy Subjects
Completed
Has Results
Obesity
Obesity
Drug: Qsymia|Drug: Placebo
Drug: Qsymia Drug: Placebo
Research Center, Lakewood, Colorado, United States
Research Center, Lakewood, Colorado, United States
A Pharmacokinetic Study Comparing VI-0521 With Placebo in Obese Adolescents
Completed
Has Results
Pediatric Obesity|Childhood Obesity
Pediatric Obesity Childhood Obesity
Drug: Placebo|Drug: VI-0521 Mid Dose|Drug: VI-0521 Top Dose
Drug: Placebo Drug: VI-0521 Mid Dose Drug: VI-0521 Top Dose
Research Facility, Baton Rouge, Louisiana, United States|Research Facility, Marrero, Louisiana, United States|Research Facility, Cincinnati, Ohio, United States|Research Facility, Charleston, South Carolina, United States
Research Facility, Baton Rouge, Louisiana, United States Research Facility, Marrero, Louisiana, United States Research Facility, Cincinnati, Ohio, United States Research Facility, Charleston, South Carolina, United States
A Study of VI-0521 for the Treatment of Obstructive Sleep Apnea / Hypopnea Syndrome in Obese Adults
Completed
Has Results
Sleep Apnea
Sleep Apnea
Drug: VI-0521|Drug: placebo
Drug: VI-0521 Drug: placebo
Kentucky Research Group, Louisville, Kentucky, United States
Kentucky Research Group, Louisville, Kentucky, United States
University of Pennsylvania Center for Weight and Eating Disorders, Philadelphia, Pennsylvania, United States
University of Pennsylvania Center for Weight and Eating Disorders, Philadelphia, Pennsylvania, United States
Real World Effectiveness of Combining an Employer-based Weight Management Program With Medication for Chronic Weight Management in Employees With Obesity
Completed
Has Results
Obesity
Obesity
Other: Weight Management Program (WMP)|Drug: Medication for chronic weight management (Rx)
Other: Weight Management Program (WMP) Drug: Medication for chronic weight management (Rx)
Novo Nordisk Investigational Site, Cleveland, Ohio, United States
Novo Nordisk Investigational Site, Cleveland, Ohio, United States
Effects of Co-administration of Canagliflozin 300 mg and Phentermine 15 mg With Placebo in the Treatment of Non-Diabetic Overweight and Obese Participants
Completed
Has Results
Obesity
Obesity
Drug: Canagliflozin|Drug: Phentermine|Drug: Matching Placebo to Canagliflozin|Drug: Matching Placebo to Phentermine
Drug: Canagliflozin Drug: Phentermine Drug: Matching Placebo to Canagliflozin Drug: Matching Placebo to Phentermine
Phoenix, Arizona, United States|Walnut Creek, California, United States|Jacksonville, Florida, United States|Meridian, Idaho, United States|Evansville, Indiana, United States|Lexington, Kentucky, United States|Louisville, Kentucky, United States|New Orleans, Louisiana, United States|Milford, Massachusetts, United States|Manlius, New York, United States|Warwick, Rhode Island, United States|Mt Pleasant, South Carolina, United States|Nashville, Tennessee, United States|Dallas, Texas, United States|Odessa, Texas, United States|Norfolk, Virginia, United States|Wauwatosa, Wisconsin, United States
Phoenix, Arizona, United States Walnut Creek, California, United States Jacksonville, Florida, United States Meridian, Idaho, United States Evansville, Indiana, United States Lexington, Kentucky, United States Louisville, Kentucky, United States New Orleans, Louisiana, United States Milford, Massachusetts, United States Manlius, New York, United States Warwick, Rhode Island, United States Mt Pleasant, South Carolina, United States Nashville, Tennessee, United States Dallas, Texas, United States Odessa, Texas, United States Norfolk, Virginia, United States Wauwatosa, Wisconsin, United States
A Multicenter, Double-blind, Randomized, Parallel-group, Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate-Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults
University of Alabama at Birmingham, Birmingham, Alabama, United States|Radiant Research - Arizona, Chandler, Arizona, United States|Scripps Clinical Research Center, La Jolla, California, United States|Translational Research Institute for Metabolism and Diabetes, Orlando, Florida, United States|Pennington Biomedical Research Center, Baton Rouge, Louisiana, United States|Boston Medical Center, Boston, Massachusetts, United States|Weill Cornell College, New York, New York, United States|Duke University, Durham, North Carolina, United States|Radiant Research - Columbus, Columbus, Ohio, United States|Radiant Research - South Carolina, Anderson, South Carolina, United States|Radiant Research - Dallas, Dallas, Texas, United States|National Clinical Research - Norfolk, Norfolk, Virginia, United States|National Clinical Research - Richmond, Richmond, Virginia, United States
University of Alabama at Birmingham, Birmingham, Alabama, United States Radiant Research - Arizona, Chandler, Arizona, United States Scripps Clinical Research Center, La Jolla, California, United States Translational Research Institute for Metabolism and Diabetes, Orlando, Florida, United States Pennington Biomedical Research Center, Baton Rouge, Louisiana, United States Boston Medical Center, Boston, Massachusetts, United States Weill Cornell College, New York, New York, United States Duke University, Durham, North Carolina, United States Radiant Research - Columbus, Columbus, Ohio, United States Radiant Research - South Carolina, Anderson, South Carolina, United States Radiant Research - Dallas, Dallas, Texas, United States National Clinical Research - Norfolk, Norfolk, Virginia, United States National Clinical Research - Richmond, Richmond, Virginia, United States
Study of VI-0521 Compared to Placebo in Treatment of Obesity in Adults
Research Site, San Diego, California, United States|Research, Ridgefield, Connecticut, United States|Research Site, Durham, North Carolina, United States|Research Site, Toledo, Ohio, United States|Research Site, Austin, Texas, United States
Research Site, San Diego, California, United States Research, Ridgefield, Connecticut, United States Research Site, Durham, North Carolina, United States Research Site, Toledo, Ohio, United States Research Site, Austin, Texas, United States
A Study to Examine the Safety, Tolerability, and Body Weight Effect of Pramlintide Alone and in Combination With Oral Antiobesity Agents in Overweight and Obese Subjects
Research Site, Birmingham, Alabama, United States|Research Site, Phoenix, Arizona, United States|Research Site, Chula Vista, California, United States|Research Site, La Jolla, California, United States|Research Site, Los Angeles, California, United States|Research Site, Walnut Creek, California, United States|Research Site, Miami, Florida, United States|Research Site, Pembroke Pines, Florida, United States|Research Site, Louisville, Kentucky, United States|Research Site, New York, New York, United States|Research Site, Raleigh, North Carolina, United States|Research Site, Statesville, North Carolina, United States|Research Site, Eugene, Oregon, United States|Research Site, Philadelphia, Pennsylvania, United States|Research Site, Austin, Texas, United States|Research Site, San Antonio, Texas, United States
Research Site, Birmingham, Alabama, United States Research Site, Phoenix, Arizona, United States Research Site, Chula Vista, California, United States Research Site, La Jolla, California, United States Research Site, Los Angeles, California, United States Research Site, Walnut Creek, California, United States Research Site, Miami, Florida, United States Research Site, Pembroke Pines, Florida, United States Research Site, Louisville, Kentucky, United States Research Site, New York, New York, United States Research Site, Raleigh, North Carolina, United States Research Site, Statesville, North Carolina, United States Research Site, Eugene, Oregon, United States Research Site, Philadelphia, Pennsylvania, United States Research Site, Austin, Texas, United States Research Site, San Antonio, Texas, United States
A VI-0521 Study to Evaluate the Long-term Safety and Efficacy in Type 2 Diabetic Adults
Completed
Has Results
Diabetes
Diabetes
Drug: Phentermine/Topiramate|Drug: Placebo
Drug: Phentermine/Topiramate Drug: Placebo
Research Site, Birmingham, Alabama, United States|Research Site, Los Angeles, California, United States|Research Site, San Francisco, California, United States|Research Site, Spring Valley, California, United States|Research Site, Walnut Creek, California, United States|Research Site, Bethesda, Maryland, United States|Research Site, Austin, Texas, United States|Research Site, San Antonio, Texas, United States|Research Site, Richmond, Virginia, United States
Research Site, Birmingham, Alabama, United States Research Site, Los Angeles, California, United States Research Site, San Francisco, California, United States Research Site, Spring Valley, California, United States Research Site, Walnut Creek, California, United States Research Site, Bethesda, Maryland, United States Research Site, Austin, Texas, United States Research Site, San Antonio, Texas, United States Research Site, Richmond, Virginia, United States
A Study to Evaluate How VI-0521 Affect Psychomotor Performance in Healthy Overweight and Obese Subjects.
Open-Label Study to Evaluate the Long-Term Safety and Efficacy of VI-0521 in Type 2 Diabetic Adults
Terminated
Has Results
Diabetes
Diabetes
Drug: VI-0521
Drug: VI-0521
Research Site, Birmingham, Alabama, United States|Research Site, Los Angeles, California, United States|Research Site, San Francisco, California, United States|Research Site, Spring Valley, California, United States|Research Site, Walnut Creek, California, United States|Research Site, Bethesda, Maryland, United States|Research Site, Austin, Texas, United States|Research Site, San Antonio, Texas, United States|Research Site, Richmond, Virginia, United States
Research Site, Birmingham, Alabama, United States Research Site, Los Angeles, California, United States Research Site, San Francisco, California, United States Research Site, Spring Valley, California, United States Research Site, Walnut Creek, California, United States Research Site, Bethesda, Maryland, United States Research Site, Austin, Texas, United States Research Site, San Antonio, Texas, United States Research Site, Richmond, Virginia, United States
Study of VI-0521 Compared to Placebo in the Glycemic Management of Obese Diabetics
Completed
Has Results
Type 2 Diabetes Mellitus
Type 2 Diabetes Mellitus
Drug: VI-0521|Drug: Placebo
Drug: VI-0521 Drug: Placebo
Research Site, Birmingham, Alabama, United States|Research Site, Los Angeles, California, United States|Research Site, San Francisco, California, United States|Research Site, Spring Valley, California, United States|Research Site, Walnut Creek, California, United States|Research Site, Bethesda, Maryland, United States|Research Site, Austin, Texas, United States|Research Site, San Antonio, Texas, United States|Research Site, Richmond, Virginia, United States
Research Site, Birmingham, Alabama, United States Research Site, Los Angeles, California, United States Research Site, San Francisco, California, United States Research Site, Spring Valley, California, United States Research Site, Walnut Creek, California, United States Research Site, Bethesda, Maryland, United States Research Site, Austin, Texas, United States Research Site, San Antonio, Texas, United States Research Site, Richmond, Virginia, United States
Study of VI-0521 Compared to Placebo in Treatment of Diabetes and Obesity in Adults With Obesity-Related Co-Morbid Conditions
Completed
Has Results
Obesity|Type 2 Diabetes
Obesity Type 2 Diabetes
Drug: VI-0521
Drug: VI-0521
Research Site, Birmingham, Alabama, United States|Research Site, Ridgefield, Connecticut, United States|Research Site, New York, New York, United States|Research Site, Durham, North Carolina, United States|Research Site, Toledo, Ohio, United States|Research Site, Austin, Texas, United States
Research Site, Birmingham, Alabama, United States Research Site, Ridgefield, Connecticut, United States Research Site, New York, New York, United States Research Site, Durham, North Carolina, United States Research Site, Toledo, Ohio, United States Research Site, Austin, Texas, United States