Lorcaserin in Combination With XR-Naltrexone for Relapse Prevention in Opioid Use Disorder

The study proposes to recruit patients with Opioid Use Disorder (OUD) seeking treatment into
our program of outpatient detoxification and naltrexone induction followed by a
relapse-prevention treatment with Extended release-naltrexone (XR-NTX) . Eligible
participants will be randomly assigned to adjunctive treatment with lorcaserin (N = 40), or
placebo (N = 20) with weekly therapy. Lorcaserin or placebo 10 mg bid will be started on Day
1 of the study to address acute withdrawal, then maintained over the next 5 weeks, and
stopped after the second XR-naltrexone is administered. Patients will be seen twice weekly
for monitoring and offered two injections of naltrexone; at the end of oral naltrexone
induction (end of week 1) and four weeks later (week 5). The primary outcome measure will be
the proportion of patients successfully retained to receive the second naltrexone injection.
Patients retained to this point tend to stay on treatment and do well long term, hence this
is the most clinically relevant outcome to evaluate treatment initiation.

Inclusion Criteria:

- 1. Individuals between the ages of 18-60

2. Meets DSM-5 criteria of current opioid use disorder present for at least six
months, supported by a positive urine for opioids

3. Seeking treatment for opioid use disorder

4. Capable of giving informed consent and complying with study procedures

5. Not underweight; defined as BMI≥18.5

Exclusion Criteria:

1. Lifetime history of DSM-5 diagnosis of schizophrenia, schizoaffective disorder, or
bipolar disorder

2. Current DSM-5 criteria for any other psychiatric disorder that in the investigator's
judgment is unstable, would be disrupted by the study medication, or is likely to
require pharmacotherapy or psychotherapy during the study period. Concurrent treatment
with other psychotropic medication is exclusionary.

3. Individuals who meet DSM-5 criteria for any substance use disorders - severe, other
than opioid and nicotine use disorder. Physiological dependence on alcohol or
sedative-hypnotics is exclusionary.

4. A recent history of binge-use of alcohol or sedative-hypnotics (using large amounts in
a short time to severe intoxication or blackouts).

5. Pregnancy, lactation, or failure to use adequate contraceptive method in female
patients who are currently engaging in sexual activity with men.

6. Unstable medical conditions, such as AIDS, cancer, uncontrolled hypertension (blood
pressure > 140/90), uncontrolled diabetes, pulmonary hypertension or heart disease.

7. Legally mandated to participate in a substance use disorder treatment program.

8. Current or recent history of significant violent or suicidal behavior, risk for
suicide or homicide

9. Currently meets DSM-5 diagnosis for an eating disorder with low body weight (BMI <20)

10. History of accidental opioid overdose in the last three years or any other significant
history of overdose following detoxification within past 10 years defined as an
episode of opioid-induced unconsciousness, whether or not medical treatment was sought
or received.

11. Elevated liver function tests (AST and ALT > 3 times the upper limit of normal) or
impaired renal function (GFR<60 ml/min)

12. Known history of allergy, intolerance, or hypersensitivity to lorcaserin, naltrexone
or any other study medications

13. Concurrent use of migraine medications containing ergotamine (Cafergot, Ergomar) or
dihydroergotamine (Migranal), 5HT2B receptor agonists like cabergoline, or medications
metabolized by CYP2D6 (thioridazine, tamoxifen, metoprolol, aripiprazole, codeine)