Dasotraline Binge Eating Disorder Study

Phase 2

Completed

Conditions: Binge Eating Disorder

Interventions: Drug: Placebo
Drug: Dasotraline

Registration Number: NCT02564588

Lead Sponsor: Sumitomo Pharma America, Inc.

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

Detailed Description: This is a randomized, double blind, parallel group, multicenter, outpatient study evaluating the efficacy and safety of flexibly-dosed dasotraline in adults with BED using dasotraline (4, 6, and 8 mg/day) versus placebo over a 12 week treatment period.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 319

Inclusion Criteria

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.

Exclusion Criteria

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.
The subject's screening ECG shows a corrected QT interval using Fridericia's formula (QTcF) of ≥ 450 msec for male subjects or ≥ 470 msec for female subjects. Eligibility will be based on the core laboratory ECG interpretation report.
Subject has any life-time history of abuse or diversion of stimulants.
Subject has a history of allergic reaction or has a known or suspected sensitivity to any substance that is contained in the study drug formulation.
Subject has enrolled in any Phase 2 or 3 trial of psychostimulants including lisdexamfetamine dimesylate (Vyvanse®) for binge-eating disorder.
Subject is currently participating or has participated in any clinical trial within the last 90 days or has participated in more than 2 clinical trials within the past year. This includes studies using marketed compounds or devices.
Subject has previously been enrolled in a clinical trial of dasotraline (SEP 225289).
Subject is an investigational site staff member or the relative of an investigational site staff member.

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Placebo	Placebo	Placebo Comparator
Dasotraline	Dasotraline	Dasotraline 4, 6, 8 mg

Primary Outcome Measures

Name	Time	Method
Change from baseline in number of binge days (defined as days during which at least 1 binge episode occurs) per week to Week 12	12 Weeks

Secondary Outcome Measures

Name	Time	Method
Change from baseline in number of binge episodes per week to Weeks 1, 2, 3, 4, 6, 8, 10, and 12	12 Weeks
Percent of subjects with a 4-week cessation from binge eating (defined as a 100% reduction for at least 28 consecutive days in the number of binge eating episodes prior to the EOT visit)	4 weeks
Change from baseline in Clinical Global Impression-Severity (CGI S) score at Weeks 2, 4, 6, 8, 10, and 12	12 Weeks
Change from baseline in Eating Disorder Examination Questionnaire Brief Version (EDE Q7) global score and 3 subscale scores (dietary restraint, shape/weight overvaluation, and body dissatisfaction) at Weeks 4, 8, and 12	12 Weeks
Change from baseline in Yale-Brown Obsessive Compulsive Scale Modified for Binge Eating (Y BOCS BE) total score and subscale scores (obsessions and compulsions) at Weeks 2, 4, 6, 8, 10, and 12	12 Weeks
Change from baseline in Sheehan disability Scale (SDS) total score and subscale scores (school/work disability, social life disability, and family life disability at Week 12	12 Weeks
Change from baseline in Montgomery-Asberg Depression Rating Scale (MADRS) total score at Week 12	12 Weeks
Change from baseline in Hamilton Anxiety Rating Scale (HAM A) score at Week 12	12 Weeks
Change from baseline in Medical Outcomes Study 12 Item Short Form (SF 12) two component scores (physical component, mental health component) at Week 12	12 Weeks
Proportion of binge-eating responders who have ≥ 75% reduction in the number of binge eating episodes from Baseline at Week 12	12 weeks
Proportion of binge-eating responders who have ≥ 50% reduction in the number of binge eating episodes from Baseline at Week 12	12 Weeks
The incidence of overall AEs, serious AEs (SAEs), and AEs (or SAEs) leading to discontinuations	12 Weeks
Clinical laboratory evaluations (serum chemistry, hematology, and urinalysis)	12 Weeks
Clinical evaluations (vital signs, orthostatic effects, and 12 lead ECGs)	12 Weeks
Frequency and severity of suicidal ideation and suicidal behavior as assessed by the Columbia-suicide severity rating scale (C SSRS)	12 Weeks
Change and percent change from baseline in body weight at Weeks 1, 2, 3, 4, 6, 8, 10, and 12	12 Weeks
Change and percent change from baseline in BMI at Weeks 1, 2, 3, 4, 6, 8, 10, and 12	12 Weeks
Change from baseline in a fasting lipid panel (triglycerides, total cholesterol, high-density lipoprotein [HDL] cholesterol, and low-density lipoprotein [LDL] cholesterol) at Weeks 6 and 12	12 Weeks
Change from baseline in hemoglobin A1c level at Weeks 6 and 12	12 Weeks
Change from baseline in fasting glucose level at Weeks 6 and 12	12 Weeks
Change in the symptoms of withdrawal from Week 12/end of treatment (EOT) as measured by: - CSSA scores at Weeks 13, 14, and 15 - DESS scores at Weeks 13, 14, and 15 - HAM A scores at Weeks 13, 14, and 15 - MADRS scores at Weeks 13, 14, and 15.	3 Weeks	The change in symptoms of withdrawal is a time frame of 3 weeks after treatment ends (weeks 13, 14, 15)

Trial Locations

Locations (37): PCSD- Feighner Research
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San Diego, California, United States
Capstone Clinical Research
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Libertyville, Illinois, United States
Sunstone Medical Research, LLC
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Medford, Oregon, United States
Miami Research Associates
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South Miami, Florida, United States
IPS Research Company
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Oklahoma City, Oklahoma, United States
Furturesearch Trials of Dallas
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Dallas, Texas, United States
Southern California Research
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Beverly Hills, California, United States
Collaborative NeuroScience Network Inc.
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Garden Grove, California, United States
Lytle and Weiss, PLLC
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Denver, Colorado, United States
Pharmacology Research Institute
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Newport Beach, California, United States
Research Across America
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Santa Ana, California, United States
Southwestern Research, Inc.
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Beverly Hills, California, United States
Adams Clinical Trials, LLC
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Watertown, Massachusetts, United States
McLean Hospital
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Belmont, Massachusetts, United States
Cypress Medical Research Center, LLC
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Wichita, Kansas, United States
Patient Priority Clinical Sites
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Cincinnati, Ohio, United States
Neuropsychiatric Associates
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Woodstock, Vermont, United States
Midwest Clinical Research Center
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Dayton, Ohio, United States
North Star Medical Research, LLC
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Middleburg Heights, Ohio, United States
Lindner Center Of Hope
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Mason, Ohio, United States
Advanced Research Institute
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Ogden, Utah, United States
NeuroScience, Inc.
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Herndon, Virginia, United States
Psychiatric Medical Associates
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Plano, Texas, United States
Texas Center for Drug Development, Inc.
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Houston, Texas, United States
Neurotrials Research, INC.
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Atlanta, Georgia, United States
Goldpoint Clinical Research, Inc.
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Indianapolis, Indiana, United States
Summit Research Network (Seattle) LLC
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Seattle, Washington, United States
Radiant Research, Inc.
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Murray, Utah, United States
Bioscience Research, LLC
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Mount Kisco, New York, United States
Wake Research Associates
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Raleigh, North Carolina, United States
Institute of Advanced Medical Research
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Alpharetta, Georgia, United States
Segal Institute for Clinical Research
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North Miami, Florida, United States
Princeton Medical Institute, LCC
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Princeton, New Jersey, United States
Lehigh Center For Clinical Research
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Allentown, Pennsylvania, United States
St. Charles Psychiatric Associates - Midwest Research Group
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Saint Charles, Missouri, United States
Oregon Center for Clinical Investigatons, INC.
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Salem, Oregon, United States
Clinical Neuroscience Solutions, Inc.
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Orlando, Florida, United States