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Braeburn

Full company profile

uuid0000ptn

Namestring
Braeburn
Legal namestring
Braeburn Inc.
Websiteurl
braeburnrx.com
Company typeenum
Private
Founded yearint
2012
Descriptiontext

Braeburn Inc. is a U.S.-based specialty pharmaceutical company headquartered at 450 Plymouth Rd #400, Plymouth Meeting, Pennsylvania, focused exclusively on the treatment of opioid use disorder (OUD). Founded in 2012, the company develops, manufactures, and commercializes BRIXADI (buprenorphine) extended-release injection for subcutaneous use, available in weekly and monthly formulations (CIII). The proprietary extended-release injection platform, identified during development as CAM2038, sustains buprenorphine plasma levels above 0.5 ng/mL, suppressing opioid withdrawal following a single dose. Clinical evidence supporting BRIXADI includes retrospective cohort data showing 20.4% vs 7.2% six-month treatment retention versus sublingual buprenorphine (P<0.001), post-hoc analyses covering up to 30,038 patients in fentanyl-using populations, and the NIH-funded MOMs Study demonstrating 82.5% vs 72.6% illicit opioid abstinence during pregnancy (p=0.009), published in JAMA Internal Medicine in 2026-03.

The company monetizes BRIXADI through prescription pharmaceutical sales distributed via a dedicated direct sales force targeting physicians, nurse practitioners, physician assistants, pharmacists, and addiction specialists who treat OUD. Specialty pharmaceutical channels — including PBMs, insurers, and government programs — handle reimbursement, while Braeburn operates the Braeburn By Your Side patient support program (877-279-7367) and a medical information line (833-274-9234) to support adherence and clinical inquiries. Pricing is not publicly disclosed. The company supplements its commercial motion with medical conference presence (CPDD, ASCP), medical science liaisons, the Rise for Recovery Advocacy Summit, the Reframe & Reclaim docuseries, and GTM partnerships with Shatterproof, Savage Sisters, Mobilize Recovery, and other community-based recovery organizations.

Operationally, Braeburn employs 101–250 staff across functions led by President & CEO and founder Mike Derkacz, alongside CMO Joshua Cohen (MD, MPH), CFO Louis Ricigliano, CCO Paul Johnson, Chief Compliance Officer Meredith Taylor, General Counsel Brian Hirsch, and VP of Manufacturing Operations Judy Cohen. The company has raised approximately $133M in disclosed private financing, including a $110M round in January 2018 led by Wellington Capital Management with participation from Apple Tree Partners, Avista Healthcare Partners, Deerfield Capital Management, New Leaf Venture Partners, RA Capital Management, and Rock Springs Capital. The company is privately held, Delaware-incorporated, and restricted by its Terms of Use to U.S. residents, with an Investigator-Initiated Trial Program and a business development search for additional rare-disease and high-unmet-need assets.

Short descriptiontext

Braeburn is a U.S. specialty pharmaceutical company that develops and commercializes BRIXADI, an FDA-approved extended-release buprenorphine injection in weekly and monthly formulations for opioid use disorder, serving patients, healthcare providers, and pregnant and postpartum women with OUD.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersPlymouth Meeting, United States
HQ citystring
Plymouth Meeting
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
extended-release buprenorphine, opioid use disorder treatment, addiction medicine pharmaceuticals, long-acting injectable therapy, specialty pharmaceutical products
Industry1 code
1Cold, Flu, Cough & Allergy Remedies (Decongestants, Antihistamines, Cough Syrups, Lozenges)
CodeCRADAMADPrimaryYes
NAICS code1 code
  • Pharmaceutical Preparation Manufacturing325412
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Specialty Pharmaceuticals / Opioid Use Disorder Treatment
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model1 record
1Pharmaceutical Product Sales
TypeSubscription Recurring
Description

Braeburn generates revenue through the sale of its FDA-approved prescription medication BRIXADI (buprenorphine) extended-release injection. The product is available in weekly and monthly formulations for subcutaneous use in treating opioid use disorder. As a specialty pharmaceutical company, revenue is derived from product sales to healthcare providers and pharmacies.

braeburnrx.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Personnel, Supply Chain, Marketing or Sales, Technology or R&D, Operations
Pricing details1 tier
1Prescription pharmaceutical product - pricing determined through insurance and healthcare channels
ModelOtherBilling cadenceMonthly
Notes

No retail pricing publicly disclosed. Healthcare provider and patient support available through Braeburn By Your Side program (877-279-7367).

braeburnrx.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 record
1BRIXADI
Description

BRIXADI (buprenorphine) extended-release injection for subcutaneous use, a medication for opioid use disorder available in weekly and monthly formulations.

braeburnrx.com
Core offering1 text field

Braeburn develops and commercializes BRIXADI (buprenorphine) extended-release injection for subcutaneous use (CIII), available in weekly and monthly formulations, as a medication for the treatment of opioid use disorder (OUD). The company operates as a specialty pharmaceutical firm, generating revenue primarily through product sales to healthcare providers and pharmacies, supported by a patient support program (Braeburn By Your Side) and medical information services.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • 20.4% vs 7.2% 6-month treatment retention rate superiority for BRIXADI vs sublingual buprenorphine (P<0.001)
+2 more records
Product overview1 text field

Braeburn is a pharmaceutical company with a single core product: BRIXADI (buprenorphine) extended-release injection. BRIXADI is available in two formulations—weekly and monthly—providing flexible dosing options for patients with opioid use disorder. The company focuses exclusively on this medication, which is the primary therapeutic offering in their portfolio for treating opioid use disorder.

Product and service2 records
1BRIXADI Weekly (buprenorphine) Extended-Release Injection
CategoryCore pharmaceutical product
Description

Extended-release buprenorphine injection administered weekly via subcutaneous route for the treatment of opioid use disorder in adults. The only FDA-approved extended-release buprenorphine with clinical trial evidence studied in pregnant and postpartum women (NIH-funded MOMs Study).

2BRIXADI Monthly (buprenorphine) Extended-Release Injection
CategoryCore pharmaceutical product
Description

Extended-release buprenorphine injection administered monthly via subcutaneous route for the treatment of opioid use disorder in adults. Provides sustained plasma concentrations that suppress opioid withdrawal and reduces the burden of daily sublingual dosing.

Scale indicator6 records

Each record includes

Type, Value, Description, Source

Partnership8 partners
Strategic tierCoreTypeGTM or Marketing Partner
Description

National nonprofit dedicated to transforming addiction treatment in the U.S. Braeburn sponsors Shatterproof Walks in Boston, Chicago, and NYC. Partnership focuses on ending stigma of addiction and supporting individuals/families affected by OUD.

Strategic tierCoreTypeGTM or Marketing Partner
Description

Grassroots harm reduction and recovery organization in Philadelphia providing trauma-informed recovery homes, public health outreach, and education. Founded by Adam Al-Asad's sister Sarah after her recovery. Braeburn is a significant supporter.

Strategic tierMinorTypeGTM or Marketing Partner
Description

Organization expanding access to harm reduction education and resources for overdose prevention across the Philadelphia region while reducing stigma against people who use drugs.

Strategic tierMinorTypeGTM or Marketing Partner
Description

Community of hope and recovery for women offering residential treatment, intensive outpatient, medical detoxification, medications for OUD, psychiatric services, and peer support services.

Strategic tierMinorTypeGTM or Marketing Partner
Description

Nevada's statewide Recovery Community Organization providing peer recovery support, employment, transportation, and housing programs for individuals and families affected by addiction.

Strategic tierCoreTypeGTM or Marketing Partner
Description

Braeburn sponsors Mobilize Recovery Across America bus tour, a cross-country initiative during National Addiction and Mental Health Recovery Month. Collaboration supports celebrating recovery and advocacy efforts across the country.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Braeburn seeks partnerships to bring medicines or medical devices to U.S. patients, looking for new assets that address high unmet need in rare or greatly underserved markets.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Braeburn supports investigator-initiated research through its IIT Program, providing funding and/or medicinal product for proposals exploring long-acting injectable buprenorphine in underserved settings and populations.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers8 records
TypeDirect peer
Description

Indivior markets Sublocade, the first FDA-approved monthly extended-release buprenorphine injection for OUD. It is the closest direct competitor to Braeburn's BRIXADI in product format, prescriber base, and patient population.

TypeDirect peer
Description

Camurus developed the FluidCrystal technology underlying BRIXADI (originally CAM2038) and markets Buvidal, a weekly/monthly extended-release buprenorphine injection, in Europe and Australia. It is the most direct technology and product peer to Braeburn in the global ER-buprenorphine category.

TypeDirect peer
Description

Alkermes markets Vivitrol, a monthly extended-release naltrexone injection approved for both OUD and alcohol use disorder. Vivitrol competes for the same prescribers, patients, and value-based contracts as BRIXADI in the long-acting injectable MOUD market.

TypeDirect peer
Description

US WorldMeds markets Lucemyra (lofexidine), an FDA-approved non-opioid treatment for mitigation of opioid withdrawal symptoms. It addresses an adjacent step in the OUD treatment journey and targets the same prescriber audience as Braeburn.

TypeEmerging player
Description

Through its acquisition of Adapt Pharma, Emergent markets Narcan (naloxone) nasal spray, the leading opioid overdose reversal product. Narcan operates in the same OUD ecosystem as BRIXADI, addressing the public-health crisis Braeburn targets.

TypeBroad incumbent
Description

Mallinckrodt has historically been a major player in OUD and pain treatment (including generic buprenorphine products) and is a broad specialty pharma incumbent. It competes in adjacent generics and branded specialty CNS markets relevant to Braeburn's commercial environment.

TypeBroad incumbent
Description

Otsuka is a large CNS-focused pharmaceutical company with mental health and addiction-adjacent assets (e.g., Abilify franchise) and pursues specialty indications overlapping Braeburn's prescriber and advocacy ecosystem.

TypeBroad incumbent
Description

Teva markets generic sublingual buprenorphine products and previously employed Braeburn's CEO. As the dominant generic buprenorphine supplier, Teva sets the pricing baseline Braeburn must justify clinically to drive branded switching.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers2 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment4 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles13 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds2 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors7 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Braeburn

Specialty Pharmaceuticals / Opioid Use Disorder Treatmentbraeburnrx.com

Braeburn is a U.S. specialty pharmaceutical company that develops and commercializes BRIXADI, an FDA-approved extended-release buprenorphine injection in weekly and monthly formulations for opioid use disorder, serving patients, healthcare providers, and pregnant and postpartum women with OUD.

What Braeburn does

Braeburn Inc. is a U.S.-based specialty pharmaceutical company headquartered at 450 Plymouth Rd #400, Plymouth Meeting, Pennsylvania, focused exclusively on the treatment of opioid use disorder (OUD). Founded in 2012, the company develops, manufactures, and commercializes BRIXADI (buprenorphine) extended-release injection for subcutaneous use, available in weekly and monthly formulations (CIII). The proprietary extended-release injection platform, identified during development as CAM2038, sustains buprenorphine plasma levels above 0.5 ng/mL, suppressing opioid withdrawal following a single dose. Clinical evidence supporting BRIXADI includes retrospective cohort data showing 20.4% vs 7.2% six-month treatment retention versus sublingual buprenorphine (P<0.001), post-hoc analyses covering up to 30,038 patients in fentanyl-using populations, and the NIH-funded MOMs Study demonstrating 82.5% vs 72.6% illicit opioid abstinence during pregnancy (p=0.009), published in JAMA Internal Medicine in 2026-03.

The company monetizes BRIXADI through prescription pharmaceutical sales distributed via a dedicated direct sales force targeting physicians, nurse practitioners, physician assistants, pharmacists, and addiction specialists who treat OUD. Specialty pharmaceutical channels — including PBMs, insurers, and government programs — handle reimbursement, while Braeburn operates the Braeburn By Your Side patient support program (877-279-7367) and a medical information line (833-274-9234) to support adherence and clinical inquiries. Pricing is not publicly disclosed. The company supplements its commercial motion with medical conference presence (CPDD, ASCP), medical science liaisons, the Rise for Recovery Advocacy Summit, the Reframe & Reclaim docuseries, and GTM partnerships with Shatterproof, Savage Sisters, Mobilize Recovery, and other community-based recovery organizations.

Operationally, Braeburn employs 101–250 staff across functions led by President & CEO and founder Mike Derkacz, alongside CMO Joshua Cohen (MD, MPH), CFO Louis Ricigliano, CCO Paul Johnson, Chief Compliance Officer Meredith Taylor, General Counsel Brian Hirsch, and VP of Manufacturing Operations Judy Cohen. The company has raised approximately $133M in disclosed private financing, including a $110M round in January 2018 led by Wellington Capital Management with participation from Apple Tree Partners, Avista Healthcare Partners, Deerfield Capital Management, New Leaf Venture Partners, RA Capital Management, and Rock Springs Capital. The company is privately held, Delaware-incorporated, and restricted by its Terms of Use to U.S. residents, with an Investigator-Initiated Trial Program and a business development search for additional rare-disease and high-unmet-need assets.

Braeburn firmographics

Firmographics
Name
Braeburn
Legal name
Braeburn Inc.
Website
https://braeburnrx.com
Company type
Private
Founded year
2012
Operating status
Operating
Headcount range
101–250 employees
Short description
Braeburn is a U.S. specialty pharmaceutical company that develops and commercializes BRIXADI, an FDA-approved extended-release buprenorphine injection in weekly and monthly formulations for opioid use disorder, serving patients, healthcare providers, and pregnant and postpartum women with OUD.
Ownership category
akta.pro rank

Braeburn industry classification

Industry
Product category
Specialty Pharmaceuticals / Opioid Use Disorder Treatment
NAICS
Pharmaceutical Preparation Manufacturing (325412)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Cold, Flu, Cough & Allergy Remedies (Decongestants, Antihistamines, Cough Syrups, Lozenges) (CRADAMAD)

Keywords

  • Extended-release buprenorphine
  • Opioid use disorder treatment
  • Addiction medicine pharmaceuticals
  • Long-acting injectable therapy
  • Specialty pharmaceutical products

Where Braeburn is headquartered

Location

Headquarters

HQ city
Plymouth Meeting
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Braeburn business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Personnel, Supply Chain, Marketing or Sales, Technology or R&D, Operations

Revenue model

  1. Pharmaceutical Product Sales: Braeburn generates revenue through the sale of its FDA-approved prescription medication BRIXADI (buprenorphine) extended-release injection. The product is available in weekly and monthly formulations for subcutaneous use in treating opioid use disorder. As a specialty pharmaceutical company, revenue is derived from product sales to healthcare providers and pharmacies.

Pricing tiers

ModelBillingPrice
OtherMonthlyPrescription pharmaceutical product - pricing determined through insurance and healthcare channels

Go-to-market motion2 records

Distribution channels3 records

Marketing channels6 records

Braeburn product offering

Product offering

Core offering

Braeburn develops and commercializes BRIXADI (buprenorphine) extended-release injection for subcutaneous use (CIII), available in weekly and monthly formulations, as a medication for the treatment of opioid use disorder (OUD). The company operates as a specialty pharmaceutical firm, generating revenue primarily through product sales to healthcare providers and pharmacies, supported by a patient support program (Braeburn By Your Side) and medical information services.

Product overview

Braeburn is a pharmaceutical company with a single core product: BRIXADI (buprenorphine) extended-release injection. BRIXADI is available in two formulations—weekly and monthly—providing flexible dosing options for patients with opioid use disorder. The company focuses exclusively on this medication, which is the primary therapeutic offering in their portfolio for treating opioid use disorder.

Differentiator

Problem solved

Functional benefit

Brands

  • BRIXADI: BRIXADI (buprenorphine) extended-release injection for subcutaneous use, a medication for opioid use disorder available in weekly and monthly formulations.

Products and services

  • BRIXADI Weekly (buprenorphine) Extended-Release Injection Extended-release buprenorphine injection administered weekly via subcutaneous route for the treatment of opioid use disorder in adults. The only FDA-approved extended-release buprenorphine with clinical trial evidence studied in pregnant and postpartum women (NIH-funded MOMs Study).
  • BRIXADI Monthly (buprenorphine) Extended-Release Injection Extended-release buprenorphine injection administered monthly via subcutaneous route for the treatment of opioid use disorder in adults. Provides sustained plasma concentrations that suppress opioid withdrawal and reduces the burden of daily sublingual dosing.

Quantifiable outcome

  • 20.4% vs 7.2% 6-month treatment retention rate superiority for BRIXADI vs sublingual buprenorphine (P<0.001)
  • +2 more outcomes

Companies that use Braeburn

Customer profile

Named customers2 records

Segments4 records

Ideal customer profiles2 records

Braeburn technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Braeburn partnerships and signals

Strategic signal

Partnerships

Eight partnerships are on record, tiered core and minor.

  • ShatterproofcoreGTM or Marketing PartnerNational nonprofit dedicated to transforming addiction treatment in the U.S. Braeburn sponsors Shatterproof Walks in Boston, Chicago, and NYC. Partnership focuses on ending stigma of addiction and supporting individuals/families affected by OUD.
  • Savage SisterscoreGTM or Marketing PartnerGrassroots harm reduction and recovery organization in Philadelphia providing trauma-informed recovery homes, public health outreach, and education. Founded by Adam Al-Asad's sister Sarah after her recovery. Braeburn is a significant supporter.
  • The Everywhere ProjectminorGTM or Marketing PartnerOrganization expanding access to harm reduction education and resources for overdose prevention across the Philadelphia region while reducing stigma against people who use drugs.
  • Nexus Recovery CenterminorGTM or Marketing PartnerCommunity of hope and recovery for women offering residential treatment, intensive outpatient, medical detoxification, medications for OUD, psychiatric services, and peer support services.
  • Foundation for RecoveryminorGTM or Marketing PartnerNevada's statewide Recovery Community Organization providing peer recovery support, employment, transportation, and housing programs for individuals and families affected by addiction.
  • Mobilize RecoverycoreGTM or Marketing PartnerBraeburn sponsors Mobilize Recovery Across America bus tour, a cross-country initiative during National Addiction and Mental Health Recovery Month. Collaboration supports celebrating recovery and advocacy efforts across the country.
  • Pharmaceutical Product PartnersminorStrategic or Co-development PartnerBraeburn seeks partnerships to bring medicines or medical devices to U.S. patients, looking for new assets that address high unmet need in rare or greatly underserved markets.
  • Investigator-Initiated Trial PartnersminorStrategic or Co-development PartnerBraeburn supports investigator-initiated research through its IIT Program, providing funding and/or medicinal product for proposals exploring long-acting injectable buprenorphine in underserved settings and populations.

Scale indicators6 records

Recent moves6 records

Expansion highlights6 records

Braeburn competitors and assessment

Company assessment

Direct peers

  • Indivior: Indivior markets Sublocade, the first FDA-approved monthly extended-release buprenorphine injection for OUD. It is the closest direct competitor to Braeburn's BRIXADI in product format, prescriber base, and patient population.
  • Camurus: Camurus developed the FluidCrystal technology underlying BRIXADI (originally CAM2038) and markets Buvidal, a weekly/monthly extended-release buprenorphine injection, in Europe and Australia. It is the most direct technology and product peer to Braeburn in the global ER-buprenorphine category.
  • Alkermes: Alkermes markets Vivitrol, a monthly extended-release naltrexone injection approved for both OUD and alcohol use disorder. Vivitrol competes for the same prescribers, patients, and value-based contracts as BRIXADI in the long-acting injectable MOUD market.
  • US WorldMeds: US WorldMeds markets Lucemyra (lofexidine), an FDA-approved non-opioid treatment for mitigation of opioid withdrawal symptoms. It addresses an adjacent step in the OUD treatment journey and targets the same prescriber audience as Braeburn.

Emerging players

  • Emergent BioSolutions: Through its acquisition of Adapt Pharma, Emergent markets Narcan (naloxone) nasal spray, the leading opioid overdose reversal product. Narcan operates in the same OUD ecosystem as BRIXADI, addressing the public-health crisis Braeburn targets.

Broad incumbents

  • Mallinckrodt Pharmaceuticals: Mallinckrodt has historically been a major player in OUD and pain treatment (including generic buprenorphine products) and is a broad specialty pharma incumbent. It competes in adjacent generics and branded specialty CNS markets relevant to Braeburn's commercial environment.
  • Otsuka Pharmaceutical: Otsuka is a large CNS-focused pharmaceutical company with mental health and addiction-adjacent assets (e.g., Abilify franchise) and pursues specialty indications overlapping Braeburn's prescriber and advocacy ecosystem.
  • Teva Pharmaceutical Industries: Teva markets generic sublingual buprenorphine products and previously employed Braeburn's CEO. As the dominant generic buprenorphine supplier, Teva sets the pricing baseline Braeburn must justify clinically to drive branded switching.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights6 records

Customer concentration

Braeburn social profiles

Digital presence

Braeburn financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Braeburn leadership team

Management profile

Number of profiles

Profiles13 records

Braeburn funding detail

Funding detail

Funding overview

Funding rounds2 records

Investors7 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Braeburn M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Braeburn

What does Braeburn do?

Braeburn develops and commercializes BRIXADI (buprenorphine) extended-release injection for subcutaneous use (CIII), available in weekly and monthly formulations, as a medication for the treatment of opioid use disorder (OUD). The company operates as a specialty pharmaceutical firm, generating revenue primarily through product sales to healthcare providers and pharmacies, supported by a patient support program (Braeburn By Your Side) and medical information services.

Is Braeburn a public or private company?

Braeburn is a private company. It is classified as venture growth investor backed and is currently operating.

When was Braeburn founded?

Braeburn was founded in 2012. It employs 101 to 250 people.

Where is Braeburn based?

Braeburn is headquartered in Plymouth Meeting, United States, in the North America region.

How does Braeburn make money?

One revenue line is on record: pharmaceutical Product Sales.

Who are Braeburn's main competitors?

Direct peers on record are Indivior, Camurus, Alkermes and US WorldMeds. Emergent BioSolutions is listed as an emerging player. Broad incumbents are Mallinckrodt Pharmaceuticals, Otsuka Pharmaceutical and Teva Pharmaceutical Industries.

Does Braeburn have an API?

No public API is recorded for Braeburn.

What industry is Braeburn in?

Braeburn's product category is Specialty Pharmaceuticals / Opioid Use Disorder Treatment. Its primary akta.pro industry code is CRADAMAD, Cold, Flu, Cough & Allergy Remedies (Decongestants, Antihistamines, Cough Syrups, Lozenges). Its NAICS code is 325412 and its SIC code is 2834.

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Live signals
PR NewswireBraeburn to Present Research at CPDD 2026 Annual Meeting, Including Data on Withdrawal Suppression and Real-World Treatment Retention in Patients With Opioid Use DisorderBraeburn announced it will present two oral presentations and two posters at the 88th Annual Scientific Meeting of the College on Problems of Drug Dependence in Portland, Oregon (June 13–17, 2026), showcasing clinical and real-world evidence for its opioid use disorder treatment BRIXADI. The presentations include findings from a post hoc analysis on first dose withdrawal suppression with injectable buprenorphine and a retrospective study showing superior 6-month treatment retention rates for BRIXADI compared to sublingual buprenorphine in patients with recent fentanyl use. The research aims to expand the clinical evidence base for BRIXADI in the context of high-potency synthetic opioids.PR NewswireBraeburn Presents New Data at 2026 ASCP Annual Meeting Demonstrating Opioid Withdrawal Suppression at Low Buprenorphine Plasma ConcentrationsBraeburn Inc. presented three poster studies at the 2026 American Society of Clinical Psychopharmacology Annual Meeting in Miami, Florida, showcasing clinical and real-world evidence for BRIXADI (buprenorphine) extended-release injection in treating opioid use disorder. A post-hoc analysis found opioid withdrawal suppression was sustained even at buprenorphine plasma concentrations below 0.5 ng/mL, while a retrospective cohort study demonstrated higher treatment retention rates for BRIXADI compared to sublingual buprenorphine at 6 months (20.4% vs 7.2%). Real-world specialty pharmacy data covering over 30,000 patients revealed evolving utilization patterns, with 60.8% of BRIXADI Weekly initiators later switching to Monthly formulations.PR NewswireNIH-Funded Randomized Clinical Trial Evaluating Weekly BRIXADI® for Opioid Use Disorder in Pregnancy and 12-months Postpartum Published in JAMA Internal MedicineBraeburn announced that results from an NIH-funded, 13-site randomized clinical trial evaluating weekly BRIXADI (extended-release buprenorphine) for opioid use disorder in pregnancy and 12-months postpartum were published in JAMA Internal Medicine. The trial met its primary endpoint of noninferiority and demonstrated statistically significant superiority over sublingual buprenorphine in illicit opioid abstinence during pregnancy (82.5% vs 72.6%, p=0.009), with fewer serious adverse events in the extended-release group during both pregnancy (8.7% vs 26.8%) and postpartum (6.0% vs 18.6%). This is the first randomized clinical trial to evaluate extended-release buprenorphine in pregnant and postpartum individuals with opioid use disorder, providing clinicians and patients with new evidence to guide treatment decisions.Morningstar/C O R R E C T I O N — Braeburn/Braeburn announced results from an NIH-funded randomized clinical trial (MOMs Study) published in JAMA Internal Medicine, evaluating weekly BRIXADI (extended-release buprenorphine) against sublingual buprenorphine for opioid use disorder in pregnancy and 12-months postpartum. The trial met its primary endpoint of noninferiority and demonstrated statistically significant superiority, with higher rates of illicit opioid abstinence during pregnancy (82.5% vs 72.6%, p=0.009) and fewer serious adverse events compared to sublingual treatment. The study, conducted at 13 U.S. sites from July 2020 to November 2024, is the first randomized clinical trial to evaluate extended-release buprenorphine in this patient population.PR NewswireBraeburn Debuts Inspiring Docuseries Celebrating Advocates Uplifting Communities to Combat the Opioid CrisisBraeburn Inc. announced the launch of a three-part docuseries titled "Reframe and Reclaim: Shaping the Future of Recovery Stories," featuring eight Philadelphia-based advocates working to destigmatize opioid use disorder and raise community awareness. The series, produced as a public health initiative, highlights personal recovery journeys and coordinated care approaches to address barriers in addiction treatment. The content is available on the Braeburn website and YouTube channel, with the company's CEO emphasizing the importance of amplifying voices from the addiction and recovery community.PR NewswireFDA Approves New Buprenorphine Treatment Option for Opioid Use DisorderThe U.S. Food and Drug Administration approved Brixadi (buprenorphine) extended-release injection for subcutaneous use to treat moderate to severe opioid use disorder. The drug is available in weekly doses (8-32 mg) and monthly doses (64-128 mg), offering new dosing flexibility for patients who have started or are already being treated with buprenorphine. The FDA granted approval of Brixadi to Braeburn Inc., and the medication will be available through a Risk Evaluation and Mitigation Strategy program administered only by healthcare providers in clinical settings.PR NewswireFDA Accepts Braeburn's New Drug Application Resubmission for BRIXADI™ (buprenorphine) Extended-Release Subcutaneous Injection for Moderate to Severe Opioid Use DisorderBraeburn announced that the FDA has accepted its New Drug Application resubmission for BRIXADI (buprenorphine) extended-release weekly and monthly injection for moderate to severe opioid use disorder, with a PDUFA action date set for December 15, 2021. BRIXADI is an investigational treatment that, if approved, would provide healthcare providers with another dosing option for treating patients with opioid use disorder as part of a complete treatment plan including counseling and psychosocial support. The FDA's acceptance of the NDA application represents a positive regulatory milestone advancing the drug toward potential approval.PR NewswireCamurus announces Braeburn resubmits New Drug Application for Brixadi™ in the USCamurus AB announced that its US licensee Braeburn has resubmitted the New Drug Application for Brixadi (buprenorphine) extended-release weekly and monthly injections for opioid use disorder treatment to the FDA. The resubmission responds to a Complete Response Letter issued in December 2020 citing deficiencies at Braeburn's third-party manufacturer. A PDUFA action date is expected from the FDA within 30 days.PR NewswireBraeburn Resubmits New Drug Application for BRIXADI™ (buprenorphine) Extended-Release Subcutaneous Injection for Moderate to Severe Opioid Use DisorderBraeburn has resubmitted its New Drug Application for BRIXADI (buprenorphine) extended-release injection to the FDA for the treatment of moderate to severe opioid use disorder. The resubmission addresses a Complete Response Letter issued in December that cited manufacturing deficiencies at a third-party facility, which have now been resolved. The company expects to receive a PDUFA date within 30 days.PR NewswireBraeburn Announces Arbitration Determination that It Did Not Materially Breach Its License Agreement with Camurus ABAn ICC tribunal ruled that Braeburn did not materially breach its license agreement with Camurus AB, allowing Braeburn to retain all North American development and commercialization rights for an extended-release buprenorphine product. The decision follows an arbitration hearing initiated by Braeburn in response to a material breach notice from Camurus. While the ruling is final regarding substantive allegations, a decision on legal cost allocation has been reserved.