FDA Approved Medication to Reduce Binge Eating and/or Purging

Bulimia Nervosa Clinical Trial

Official title:

Qsymia (Phentermine-topiramate) to Reduce Binge Eating/Purging in Patients With Bulimia Nervosa and Binge Eating Disorder

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02553824
• Other study ID #: 31390
• Status: Completed
• Phase: Phase 1
• Start date: October 30, 2015
• Est. completion date: April 15, 2017

Study information

• Verified date: May 2018
• Source: Stanford University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will demonstrate the efficacy of Qsymia versus placebo in treating bulimia nervosa and binge eating disorder.

Description:

Bulimia nervosa (BN) and binge eating disorder (BED) are serious mental disorders associated with adverse psychological and physical consequences. Treatment options to date offer limited success, leaving at least 50-70% of patients still symptomatic after treatment. The purpose of the study is to evaluate whether phentermine-topiramate (Qsymia), a medication currently FDA approved for the treatment of obesity, will demonstrate efficacy—compared to placebo- when re-purposed for patients with bulimia and binge eating.

Participants will be randomized into one of two conditions: qsymia or Placebo. One condition will receive 3 months of phentermine-topiramate, a 2 week washout, then 3 months of placebo. The other condition will receive 3 months of Placebo, a 2 week washout, then 3 months of phentermine-topiramate. Participants will receive a total of 6 months of treatment and then have a 2 month follow-up off of medications.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 22
• Est. completion date: April 15, 2017
• Est. primary completion date: February 23, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

• Must meet Diagnostic and Statistical Manual -Edition 5 criteria for bulimia or binge eating disorder, which has not responded to prior treatment

• Men and women between the ages of 18-60

• Must be at least normal weight (i.e. body mass index at least 21.0 or greater)

• If female of child-bearing potential, the participant must have an initial negative pregnancy test and be taking adequate birth control

• must be medically stable with no new diagnoses (medical, surgical, or psychiatric) within the past 6 months

• Must live close enough or be within commute distance of study site (Stanford, CA) to be able to comply with study visits, treatment plans, and blood draws and other possible assessments (i.e. EKG)

Exclusion Criteria:

• Any patient with bipolar disease or schizophrenia or any patient taking a mood stabilizer or antipsychotic medication within the past 3 months

• Any patient with current or past history of anorexia nervosa (i.e., with a Body mass index of < 17.5).

• Any patient with prior (within 30 days) use of Over The Counter (OTC) weight-reducing agents, herbal preparations

• Any patient who has been prescribed a medication for weight loss within the past 3 months

• Any psychological weight-loss interventions (i.e., Weight Watchers, Jenny Craig) in which patient has lost weight over the past month (unless willing to discontinue).

• Any patient currently in therapy with a psychostimulant or who has used a psychostimulant within the past 6 months

• Any patient with known sensitivity to phentermine or topiramate

• Any patient who has had a change in thyroid, psychiatric, or blood pressure medications within the past one month

• Any patient who is taking a potassium-wasting diuretic

• Any patient who is on a carbonic anhydrase inhibitor such as zonisamide acetazolamide, or dichlorphenamide

• Any diabetic who is taking insulin or an insulin secretagogue

• Any patient with liver enzymes at baseline greater than three times the upper limit of normal

• Any patient with a baseline potassium of less than 3.0 millequivalent/Liter. Patients with baseline potassium levels between 3.0-3.5 miliEquivalents/Liter will be encouraged to ingest high potassium foods such as bananas, oranges, or tomato juice daily during the study

• Any patient with abnormal baseline thyroid test or with a Thyroid Stimulating Hormone (TSH) greater than 1.5 times the upper limit of normal

• Any patient who is unwilling or expresses uncertainty about being able to refrain from daily alcohol use (even if at moderate levels) or illegal drugs while taking the study medication.

• Any adult with recent history of suspected alcohol or substance abuse or substance dependence

• Any patient who regularly uses marijuana (including medical marijuana) or illegal drugs

• Any patient who has a history of addiction to a stimulant

• Any patient who expresses current suicidal ideation

• Any patient with a history of nephrolithiasis

• Any patient who is pregnant or who is planning to become pregnant during the study period.

• Any patient who is currently participating in any other clinical study that involves an active treatment

• Any patient who is unable to identify a primary care physician

• Any patient with a history of cardiovascular disease (i.e. recent history of Myocardial Infarction, stroke, shortness of breath, chest pain) that could increase vulnerability to the sympathomimetic effects of a stimulant like drug. If clinical suspicion is high, baseline EKG will be obtained and anyone with abnormal findings will be excluded

Related Conditions & MeSH terms

• Binge Eating Disorder
• Binge-Eating Disorder
• Bulimia
• Bulimia Nervosa
• Feeding and Eating Disorders

Intervention

Drug:
• Phentermine/Topiramate-First
Patients randomly assigned to this Arm will have a 4 week ramp up period (in which doses will be increased, as tolerated, starting from 3.75 mg/23 mg, 7.5 mg/46 mg ,11.25 mg/69 mg , 15 mg/92 mg taken once daily in the morning. For the final 8 weeks, participants will take the 15mg/92 mg (or highest dose tolerated). Then will have a 2 week washout followed by a crossover to 12 weeks of control medication/ placebo.
• Placebo
Patients randomly assigned to this Arm will have begin with 12 weeks of placebo followed by a 2 week washout. They will then crossover to Qsymia and receive a 4 week ramp up period (in which doses will be increased, as tolerated, starting from 3.75 mg/23 mg, 7.5 mg/46 mg ,11.25 mg/69 mg , 15 mg/92 mg taken once daily in the morning. For the final 8 weeks, participants will take the 15mg/92 mg (or highest dose tolerated).

Locations

Country	Name	City	State
United States	Stanford School of Medicine, Psychiatry and Behavioral Sciences	Stanford	California

Sponsors (1)

Lead Sponsor	Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Frequency of binge eating episodes as measured by the Eating Disorder Examination Assessment	The primary outcome is the frequency of binge episodes	8.5 months
Secondary	Frequency of binge eating episodes measured by the Eating Disorder Examination Assessment	Frequency of binge episodes	8.5 months
Secondary	Percentage of Abstinence from Binge Eating as Measured by the Eating Disorder Examination Assessment	Percentage of patients who have had no binge episodes as assessed by the EDE	8.5 months