Dasotraline Binge Eating Disorder Study

Completed · Phase 2/Phase 3 · Has a placebo group

Conditions studied: Binge Eating Disorder

In brief

Evaluate the efficacy of flexibly-dosed dasotraline compared with placebo in adults with moderate to severe Binge Eating Disorder (BED)

Key facts

Study ID: NCT02564588
Run by: Sumitomo Pharma America, Inc.
People needed: 319
Starts: 2015-10-01
Expected to finish: 2016-10-01
Last updated by the study team: 2017-09-28

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Male or female subject between 18 and 55 years of age, inclusive, at time of informed consent.
Subject meets the following DSM 5 criteria for a diagnosis of BED. An episode of binge eating is characterized by both:
Eating an amount of food larger than what most people would eat, in a discrete period of time (eg, 2 hours)
Sense of lack of control over eating episode
Binge-eating episodes are associated with ≥ 3 of the following:
Eating much more rapidly than normal
Eating until uncomfortably full
Eating large amounts when not feeling hungry
Eating alone because of embarrassment
Feeling disgusted with oneself, guilty afterward
Binge-eating episodes are also associated with marked distress regarding the episode and not associated with recurrent use of compensatory behavior (eg, bulimia nervosa).
Diagnosis is confirmed based on the eating-disorders module of the SCID, clinician review of subject diaries, and the EDE Q.
Subject has a BED diagnosis including at least 2 binge eating days a week for at least 6 months prior to screening.
Subject's BED is of at least moderate severity.
Subject has a negative breath alcohol test and a negative urine drug screen (UDS) for any illicit drug.
Female subject must have a negative serum pregnancy test at screening; females who are post-menopausal (defined as at least 12 months of spontaneous amenorrhea) and those who have undergone hysterectomy or bilateral oophorectomy will be exempted from the pregnancy test.
Female subject of childbearing potential and male subject with female partner of childbearing potential must agree to use an effective and medically acceptable form of birth control throughout the study period. Note: Continued use of an effective and medically acceptable form of birth control is recommended for 30 days after study completion.
Subject must be able to comply with study drug administration and adhere to protocol requirements.
Subject can read well enough to understand the informed consent form and other subject materials.

You may not qualify if…

Subject has body weight index (BMI) of 18 kg/m2or less or greater than 45 kg/m2.
Subject has a lifetime history or current symptoms of bulimia nervosa or anorexia nervosa.
Subject has started psychotherapy (eg, supportive psychotherapy, cognitive behavior therapy, interpersonal therapy) within 3 months prior to screening. Note: Subjects receiving stable ongoing psychotherapy for longer than 3 months are permitted to enroll.
Subject is participating in a formal weight loss program (eg, Weight Watchers®) within 3 months prior to screening.
Subject has used a psychostimulant or mood stabilizer within the 3 months prior to screening.
Subject has used any medications for the treatment of binge eating, other eating disorders, obesity, or weight gain or any other medication that could result in weight gain or weight loss including over-the-counter and herbal products within the 3 months prior to screening.
Subject has a lifetime history of psychotic disorder, bipolar disorder, hypomania, dementia, or ADHD as defined by the DSM 5 criteria.
Subject has a history of moderate to severe depression based on investigator's judgment within the 6 months prior to screening or is currently taking or has taken any medication for depression during the 3 months prior to screening.
Subject has a history of substance use disorder including alcohol use disorder (excluding nicotine and caffeine) within the 12 months prior to screening, as defined by the DSM 5 criteria.
Subject has MADRS score ≥ 18 at screening and Baseline visit.
Subject is considered a suicide risk or has any previous history of suicide attempt.
Subject answers "yes" to "suicidal ideation" item 4 (active suicidal ideation with some intent to act, without specific plan) or item 5 (active suicidal ideation with specific plan and intent) on the C SSRS assessment at screening (in the past month). Subjects who answer "yes" to this question must be referred to the Investigator for follow up evaluation.
Subject has type I diabetes mellitus or insulin-dependent diabetes mellitus.
Subject with type II diabetes mellitus has hemoglobin A1c ≥ 6.5% at screening, or has initiated treatment with or changed the dose of a glucose-lowering agent within 3 months prior to screening.
Subject has known history of symptomatic cardiovascular disease, advanced arteriosclerosis, structural cardiac abnormality, cardiomyopathy, documented heart rhythm abnormalities, coronary artery disease, or other serious cardiac problems.
Subject has initiated treatment with or changed the dose of a lipid-lowering medication within the 3 months prior to screening.
Subject has a history of moderate or severe hypertension that in the investigator's opinion has not been medically stable or has required a change in dosage and/or medication during the 3 months prior to screening.
Subject has a history of epilepsy, seizures (except childhood febrile seizures), unexplained syncope or other unexplained blackouts (except single incident), or head trauma with loss of consciousness lasting more than 5 minutes, or a history of clinically significant repeated head-traumas without loss of consciousness.
Subject is female and pregnant or nursing.
Subject has had bariatric surgery, lap bands, duodenal stents, or other procedures for weight loss.
Subject has a history of positive test for Hepatitis B surface antigen or Hepatitis C antibody with liver function test results at screening above the upper limit of normal (ULN) for the reference laboratory.
Subject without a history of positive test for Hepatitis B surface antigen or Hepatitis C antibody has alanine aminotransferase (ALT) or aspartate aminotransferase (AST) value ≥ 2 times the ULN at screening.
Subject has a blood urea nitrogen (BUN) value ≥ 1.5 times the ULN for the reference range, fasting blood glucose ≥ 126 mg/dL (7.0 mmol/L), or hemoglobin A1c ≥ 6.5% at screening.
Subject is known to have tested positive for human immunodeficiency virus (HIV).
Subject has a clinically significant abnormality on screening evaluation including physical examination, vital signs, ECG, or laboratory tests that the investigator considers to be inappropriate to allow participation in the study.

Where it is running

Southern California Research — Beverly Hills, California, United States
Southwestern Research, Inc. — Beverly Hills, California, United States
Pharmacology Research Institute — Encino, California, United States
Collaborative NeuroScience Network Inc. — Garden Grove, California, United States
Pharmacology Research Institute — Newport Beach, California, United States
PCSD- Feighner Research — San Diego, California, United States
Research Across America — Santa Ana, California, United States
Lytle and Weiss, PLLC — Denver, Colorado, United States
Clinical Neuroscience Solutions, Inc. — Jacksonville, Florida, United States
Segal Institute for Clinical Research — North Miami, Florida, United States
Clinical Neuroscience Solutions, Inc. — Orlando, Florida, United States
Miami Research Associates — South Miami, Florida, United States
Institute of Advanced Medical Research — Alpharetta, Georgia, United States
Neurotrials Research, INC. — Atlanta, Georgia, United States
Capstone Clinical Research — Libertyville, Illinois, United States
Goldpoint Clinical Research, Inc. — Indianapolis, Indiana, United States
Cypress Medical Research Center, LLC — Wichita, Kansas, United States
McLean Hospital — Belmont, Massachusetts, United States
Adams Clinical Trials, LLC — Watertown, Massachusetts, United States
St. Charles Psychiatric Associates - Midwest Research Group — Saint Charles, Missouri, United States
Princeton Medical Institute, LCC — Princeton, New Jersey, United States
Bioscience Research, LLC — Mount Kisco, New York, United States
Wake Research Associates — Raleigh, North Carolina, United States
Radiant Research, Inc. — Akron, Ohio, United States
Patient Priority Clinical Sites — Cincinnati, Ohio, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.