Overview
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.
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)
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2025/05/15 | Phase 1 | Active, not recruiting | |||
2025/05/04 | Not Applicable | Active, not recruiting | Asad Ullah Jan | ||
2024/11/07 | Phase 1 | Completed | |||
2024/11/05 | Phase 4 | Recruiting | |||
2024/09/24 | Phase 1 | Recruiting | |||
2024/08/22 | Not Applicable | Not yet recruiting | |||
2024/08/21 | Phase 1 | Active, not recruiting | |||
2024/04/18 | Phase 1 | Recruiting | |||
2024/04/16 | Phase 1 | Completed | |||
2024/02/12 | Phase 4 | Recruiting |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Sun Pharmaceutical Industries, Inc. | 47335-736 | ORAL | 100 mg in 1 1 | 1/10/2023 | |
Bausch Health US LLC | 0187-0730 | ORAL | 150 mg in 1 1 | 3/4/2022 | |
CIPLA USA INC., | 69097-917 | ORAL | 75 mg in 1 1 | 3/27/2023 | |
STAT Rx USA LLC | 16590-246 | ORAL | 300 mg in 1 1 | 8/22/2012 | |
NuCare Pharmaceuticals,Inc. | 68071-2577 | ORAL | 100 mg in 1 1 | 7/17/2023 | |
Chartwell RX, LLC | 62135-875 | ORAL | 150 mg in 1 1 | 4/5/2024 | |
Lupin Pharmaceuticals, Inc. | 68180-320 | ORAL | 300 mg in 1 1 | 4/19/2023 | |
AvPAK | 50268-142 | ORAL | 75 mg in 1 1 | 1/9/2024 | |
Actavis Pharma, Inc. | 0591-3543 | ORAL | 150 mg in 1 1 | 3/21/2023 | |
REMEDYREPACK INC. | 70518-2641 | ORAL | 100 mg in 1 1 | 3/24/2025 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
---|---|---|---|
Authorised | 3/26/2015 |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
WELLBUTRIN SR TABLETS 150 mg | SIN10983P | TABLET, FILM COATED | 150 mg | 6/16/1999 | |
CONTRAVE PROLONGED RELEASE TABLET 8MG/90MG | SIN16411P | TABLET, FILM COATED, EXTENDED RELEASE | 90mg | 1/3/2022 |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
---|---|---|---|---|---|
Bupropion Hydrochloride Tablets | 国药准字H20051823 | 化学药品 | 片剂 | 6/30/2020 | |
Bupropion Hydrochloride Tablets | 国药准字H20070209 | 化学药品 | 片剂 | 11/15/2021 | |
Bupropion Hydrochloride Sustained-release Tablets | 国药准字H20203582 | 化学药品 | 片剂 | 11/17/2020 | |
Bupropion Hydrochloride Sustained-release Tablets | 国药准字H20080111 | 化学药品 | 片剂 | 2/14/2023 | |
Bupropion Hydrochloride Sustained-release Tablets | 国药准字H20090221 | 化学药品 | 片剂 | 5/22/2019 | |
Bupropion Hydrochloride Sustained-release Tablets | 国药准字H20080398 | 化学药品 | 片剂 | 10/12/2021 | |
Bupropion Hydrochloride Sustained-release Tablets | 国药准字H20203581 | 化学药品 | 片剂 | 11/17/2020 | |
Bupropion Hydrochloride Sustained-release Tablets | 国药准字H20055847 | 化学药品 | 片剂 | 8/17/2020 | |
Bupropion Hydrochloride Sustained-release Tablets | 国药准字H20203580 | 化学药品 | 片剂 | 11/17/2020 | |
Bupropion Hydrochloride Sustained-release Tablets | 国药准字H20080344 | 化学药品 | 片剂 | 12/22/2022 |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
---|---|---|---|---|---|
WELLBUTRIN XL EXTENDED RELEASE TAB 300 MG | N/A | N/A | N/A | 8/21/2009 | |
CONTRAVE PROLONGED-RELEASE TABLETS 8MG/90MG | N/A | N/A | N/A | 12/10/2020 | |
WELLBUTRIN XL EXTENDED RELEASE TAB 150MG | N/A | N/A | N/A | 9/14/2009 |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
ZYBAN SR bupropion hydrochloride 150mg tablet blister pack | 75233 | Medicine | A | 8/22/2000 | |
CONTRAVE 8/90 naltrexone hydrochloride 8 mg and bupropion hydrochloride 90 mg modified-release tablet blister pack | 288372 | Medicine | A | 8/24/2018 |