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269,912 Results for "braeburn pharmaceutical".
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Drug Development
Braeburn Announces Publication of a Post Hoc Analysis of Data from Patients Using Fentanyl Treated with BRIXADI in a Phase 3 Efficacy and Safety Study
Braeburn Inc. announces the publication of a post hoc analysis in the Journal of the American Medical Association (JAMA) Network Open.
June 25, 2024
·
12 min read
FDA
Braeburn’s Long-Acting Brixadi Receives FDA Clearance to Treat Opioid Use Disorder
The FDA approved Braeburn Pharmaceuticals’ new buprenorphine treatment option with extended-release medication that could pave the way for greater patient compliance.
May 25, 2023
·
3 min read
·
Lisa Munger
Pharm Country
Braeburn’s BRIXADI™ (buprenorphine) Extended-Release Subcutaneous Injection (CIII) Receives FDA Approval for Moderate to Severe Opioid Use Disorder
Braeburn announces that the U.S. Food and Drug Administration (FDA) has approved BRIXADI (buprenorphine) extended-release injection for subcutaneous use (CIII), a new weekly and monthly medication for moderate to severe opioid use disorder (OUD).
May 23, 2023
·
12 min read
Press Releases
Avadel Pharmaceuticals to Present at Upcoming September 2025 Investor Conferences
September 1, 2025
·
1 min read
Press Releases
Niagen Bioscience Announces Pharmaceutical-Grade Niagen® IV Is Now Available in Almost 600 Clinics Nationwide
May 5, 2025
·
11 min read
Press Releases
Eledon Pharmaceuticals to Participate in Cantor Global Healthcare Conference 2025
August 29, 2025
·
1 min read
Press Releases
Salarius Pharmaceuticals Regains Compliance with Nasdaq Minimum Bid Price Requirement
September 10, 2025
·
7 min read
Press Releases
Apellis Pharmaceuticals to Participate in Upcoming September 2025 Investor Conferences
August 28, 2025
·
1 min read
Press Releases
Genix Pharmaceuticals Closes Private Placement
September 4, 2025
·
3 min read
Camurus announces Braeburn resubmits New Drug Application for Brixadi™ in the US
Camurus AB (NASDAQ STO: CAMX) today announced that its US licensee Braeburn has resubmitted the New Drug Application (NDA) for Brixadi 1 (buprenorphine) extended-release weekly and monthly injections for the treatment of moderate to severe opioid use disorder to the US Food and Drug Administration (FDA).
June 15, 2021
·
1 min read
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