MedPath

Bupropion

Generic Name
Bupropion
Brand Names
Aplenzin, Auvelity, Budeprion, Contrave, Forfivo, Wellbutrin, Zyban
Drug Type
Small Molecule
Chemical Formula
C13H18ClNO
CAS Number
34911-55-2
Unique Ingredient Identifier
01ZG3TPX31
Background

Bupropion (also known as the brand name product Wellbutrin®) is a norepinephrine/dopamine-reuptake inhibitor (NDRI) used most commonly for the management of Major Depressive Disorder (MDD), Seasonal Affective Disorder (SAD), and as an aid for smoking cessation. Bupropion exerts its pharmacological effects by weakly inhibiting the enzymes involved in the uptake of the neurotransmitters norepinephrine and dopamine from the synaptic cleft, therefore prolonging their duration of action within the neuronal synapse and the downstream effects of these neurotransmitters. More specifically, bupropion binds to the norepinephrine transporter (NET) and the dopamine transporter (DAT).

Bupropion was originally classified as an "atypical" antidepressant because it does not exert the same effects as the classical antidepressants such as Monoamine Oxidase Inhibitors (MAOIs), Tricyclic Antidepressants (TCAs), or Selective Serotonin Reuptake Inhibitors (SSRIs). While it has comparable effectiveness to typical first-line options for the treatment of depression such as SSRIs, bupropion is a unique option for the treatment of MDD as it lacks any clinically relevant serotonergic effects, typical of other mood medications, or any effects on histamine or adrenaline receptors. Lack of activity at these receptors results in a more tolerable side effect profile; bupropion is less likely to cause sexual side effects, sedation, or weight gain as compared to SSRIs or TCAs, for example.

When used as an aid to smoking cessation, bupropion is thought to confer its anti-craving and anti-withdrawal effects by inhibiting dopamine reuptake, which is thought to be involved in the reward pathways associated with nicotine, and through the antagonism of the nicotinic acetylcholinergic receptor. A Cochrane Review of meta-analyses of available treatment modalities for smoking cessation found that abstinence rates approximately doubled when bupropion was used as compared to placebo, and was found to have similar rates of smoking cessation as nicotine replacement therapy (NRT).

Bupropion is sometimes used as an add-on agent to first-line treatments of depression such as selective serotonin reuptake inhibitor (SSRI) medications when there is a treatment-failure or only partial response. Bupropion is also used off-label for the management of Attention/Deficit-Hyperactivity Disorder (ADHD) in adults with comorbid bipolar depression to avoid mood destabilization caused by typical stimulant medications used for the treatment of ADHD.

When used in combination with naltrexone in the marketed product ContraveⓇ for chronic weight management, the two components are thought to have effects on areas of the brain involved in the regulation of food intake. This includes the hypothalamus, which is involved in appetite regulation, and the mesolimbic dopamine circuit, which is involved in reward pathways. Studies have shown that the combined activity of bupropion and naltrexone increase the firing rate of hypothalamic pro-opiomelanocortin (POMC) neurons and blockade of opioid receptor-mediated POMC auto-inhibition, which are associated with a reduction in food intake and increased energy expenditure. The combination of naltrexone and bupropion was shown to result in a statistically significant weight loss, with a mean change in body weight of -6.3% compared to -1.3% for placebo.

Indication

Bupropion is indicated for the treatment of major depressive disorder (MDD), seasonal affective disorder (SAD), and as an aid to smoking cessation.

When used in combination with naltrexone as the marketed product ContraveⓇ, bupropion is indicated as an adjunct to a reduced-calorie diet and increased physical activity for chronic weight management in adults with an initial body mass index (BMI) of: 30 kg/m^2 or greater (obese) or 27 kg/m^2 or greater (overweight) in the presence of at least one weight-related comorbid condition (e.g., hypertension, type 2 diabetes mellitus, or dyslipidemia).

Bupropion is also used off-label as a first-line treatment in patients with ADHD and comorbid bipolar disorder when used as an adjunct to mood stabilizers.

Associated Conditions
Attention Deficit Hyperactivity Disorder (ADHD), Major Depressive Disorder (MDD), Obesity, Seasonal Affective Disorder (SAD)
Associated Therapies
Smoking, Cessation, Weight Loss

Trial of Naltrexone/Bupropion for the Treatment of Methamphetamine Use Disorder

Phase 3
Recruiting
Conditions
Methamphetamine Abuse
Methamphetamine-dependence
Interventions
First Posted Date
2024-01-31
Last Posted Date
2024-12-10
Lead Sponsor
National Institute on Drug Abuse (NIDA)
Target Recruit Count
360
Registration Number
NCT06233799
Locations
🇺🇸

University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States

🇺🇸

University of California Los Angeles, Los Angeles, California, United States

🇺🇸

University of California at San Diego, San Diego, California, United States

and more 7 locations

A Study to Evaluate the Efficacy of AXS-05 Compared to Bupropion in Preventing the Relapse of Depressive Symptoms

Phase 4
Recruiting
Conditions
Major Depressive Disorder
Interventions
First Posted Date
2024-01-25
Last Posted Date
2025-01-23
Lead Sponsor
Axsome Therapeutics, Inc.
Target Recruit Count
350
Registration Number
NCT06223880
Locations
🇺🇸

Clinical Research Site, Everett, Washington, United States

Voxelotor CYP and Transporter Cocktail Interaction Study

First Posted Date
2023-08-08
Last Posted Date
2024-11-22
Lead Sponsor
Pfizer
Target Recruit Count
44
Registration Number
NCT05981365
Locations
🇺🇸

ICON Early Phase Services, LLC, San Antonio, Texas, United States

Phase Ib/2a Drug-drug Interaction Study of a Combination of 45mg Dextromethorphan With 105 mg Bupropion

Phase 1
Recruiting
Conditions
Addiction
Opioid Use
Substance Use Disorders
Opioid Use Disorder
Interventions
Drug: Placebo
First Posted Date
2023-08-04
Last Posted Date
2024-12-24
Lead Sponsor
Virginia Commonwealth University
Target Recruit Count
18
Registration Number
NCT05976646
Locations
🇺🇸

CARI Research Clinic- VCU Institute for Drug and Alcohol Studies, Richmond, Virginia, United States

The Effect of a Six Week Intensified Pharmacological Treatment for Bipolar Depression Compared to Treatment as Usual in Subjects Who Had a First-time Treatment Failure on Their First-line Treatment.

First Posted Date
2023-08-03
Last Posted Date
2025-05-16
Lead Sponsor
Dr. Inge Winter
Target Recruit Count
418
Registration Number
NCT05973786
Locations
🇦🇹

Medical University Innsbruck, Innsbruck, Austria

🇩🇪

Universitätsklinik für Psychiatrie und Psychotherapie Bielefeld, Bielefeld, Germany

🇩🇪

Klinik für Psychiatrie und Psychotherapie der Universitätsmedizin Mainz, Mainz, Germany

and more 10 locations

A Study to Assess the Effect of BMS-986419 on the Single Dose Drug Levels of Probe Substrates in Healthy Participants

First Posted Date
2023-07-06
Last Posted Date
2023-10-30
Lead Sponsor
Bristol-Myers Squibb
Target Recruit Count
22
Registration Number
NCT05932277
Locations
🇺🇸

ICON Lenexa, Lenexa, Kansas, United States

Improving Smoking Abstinence Outcomes in the African American Community Through Extended Treatment

Phase 3
Recruiting
Conditions
Smoking Cessation
Interventions
First Posted Date
2023-02-17
Last Posted Date
2025-03-10
Lead Sponsor
University of Kansas Medical Center
Target Recruit Count
500
Registration Number
NCT05732272
Locations
🇺🇸

University of Kansas Medical Center, Kansas City, Missouri, United States

Intensified Pharmacological Treatment for Schizophrenia, Major Depressive Disorder and Bipolar Depression After a First-time Treatment Failure

Phase 3
Recruiting
Conditions
Major Depressive Disorder
Bipolar Depression
Schizophrenia and Related Disorders
Interventions
First Posted Date
2022-11-02
Last Posted Date
2025-05-18
Lead Sponsor
Dr. Inge Winter
Target Recruit Count
1254
Registration Number
NCT05603104
Locations
🇮🇱

Sheba Medical Center, Ramat Gan, Israel

A Study to Assess the Efficacy and Safety of AXS-05 in Subjects with Alzheimer's Disease Agitation

Phase 3
Completed
Conditions
Agitation in Patients with Dementia of the Alzheimer's Type
Alzheimer Disease
Agitation
Interventions
Drug: Placebo
First Posted Date
2022-09-28
Last Posted Date
2025-01-17
Lead Sponsor
Axsome Therapeutics, Inc.
Target Recruit Count
408
Registration Number
NCT05557409
Locations
🇵🇷

Clinical Research Site, San Juan, Puerto Rico

SMART Trial to Predict Anhedonia Response to Antidepressant Treatment

Phase 4
Recruiting
Conditions
Major Depressive Disorder
Interventions
First Posted Date
2022-09-13
Last Posted Date
2023-10-04
Lead Sponsor
Mclean Hospital
Target Recruit Count
183
Registration Number
NCT05537584
Locations
🇺🇸

McLean Hospital, Belmont, Massachusetts, United States

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