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Braeburn s BRIXADI™ (buprenorphine) Extended-Release Subcutaneous Injection (CIII) Receives FDA Approval for Moderate to Severe Opioid Use Disorder

Braeburn s BRIXADI™ (buprenorphine) Extended-Release Subcutaneous Injection (CIII) Receives FDA Approval for Moderate to Severe Opioid Use Disorder
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Braeburn Announces Arbitration Determination that It Did Not Materially Breach Its License Agreement with Camurus AB

Braeburn Announces Arbitration Determination that It Did Not Materially Breach Its License Agreement with Camurus AB News provided by Share this article Share this article PLYMOUTH MEETING, Pa., Dec. 10, 2020 /PRNewswire/ Braeburn announces that a tribunal appointed by the ICC International Court of Arbitration decided that Braeburn did not materially breach its license agreement with Camurus for the development and commercialization of an extended-release buprenorphine subcutaneous injection product. As a result of this decision, Braeburn retains all North American development and commercialization rights to the product as described in the license agreement, which remains in full effect. This decision follows an arbitration hearing initiated by Braeburn in response to the issuance of a material breach notice from Camurus.

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