Dasotraline Binge Eating Disorder Study

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.

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.