Camurus och Braeburn Pharmaceuticals inleder fas 3-studie — Kanske i BÖRSVÄRDE: MSEK Camurus aktie (CAMX) är noterad på 

STOCKHOLM (Fonder Direkt) Läkemedelsutvecklaren Camurus aktie Samtidigt konstaterar Carnegie att Braeburn/Camurus sagt att det finns 

During this meeting  2016年11月14日 Braeburn Pharmaceuticals and Camurus Announce Positive Top-line Phase 3 Results for Long-acting Buprenorphine (CAM2038) for  Nov 2, 2017 Indivior could see competition to RBP-6000 quickly however, as Camurus and Braeburn Pharma's formulation of the drug (called CAM2038)  as Camurus/Braeburn Pharmaceuticals' CAM-2038, could, therefore, appeal to both payers and prescribers. Indeed, 86-96% of surveyed physicians are willing  Dec 10, 2018 Camurus (Lund, Sweden), a partner of Braeburn (Plymouth Meeting, PA), announced1 the positive opinion and recommendation by the  Jan 6, 2020 The company believed that the Camurus weekly and monthly depot injection products licensed by Braeburn would enable clinicians and  Apr 20, 2020 Helsinn Healthcare; Midatech/Galena Biopharma; Merck; Acacia Pharma; Cara Therapeutics; Camurus/Braeburn. For more information about  Nov 23, 2018 The European Commission (EC) has approved Camurus' weekly and of 26 December 2018 for CAM2038 to Camurus' US partner Braeburn. Jun 29, 2015 Braeburn has formed another partnership with Camurus, a Swedish drug company, to develop an injectable buprenorphine drug to treat  Jan 23, 2017 a fluid crystal depot buprenorphine therapy developed by Braeburn Pharmaceuticals and Camurus, with the current standard of care, a daily  Sep 27, 2018 Camurus' partner Braeburn will be responsible for the regulatory procedure in the US. The final decision on Buvidal will be decided by the  Pros. Braeburn has highly experienced and passionate employees.

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Nya data styrker långtidssäkerhet och  Svenska Camurus ingår ett värdefullt licensavtal. Camurus från Lund har ingått ett exklusivt licensavtal med Braeburn Pharmaceuticals för sitt  {{ $select.selected.num + '. ' +$select.selected.name }}. {{ eCtrl.event.layout.chapters.title || 'Select chapter' }}. {{ chapter.num }}. {{ chapter.name }}  {{ $select.selected.num + '. ' +$select.selected.name }}.

The primary study Camurus Announces That FDA Grants Braeburn's Citizen Petition, Eliminating the Risk of Further Blocking of Brixadi™ From the US market PRESS RELEASE PR Newswire Nov. 7, 2019, 10:29 PM Camurus AB (NASDAQ STO: CAMX) meddelade idag att den amerikanska läkemedelsmyndigheten (FDA) utfärdat en begäran till Camurus licenspartner Braeburn om ytterligare information, i form av ett Complete Response Letter (CRL), avseende registreringsansökan för Brixadi™ vecko- och månadsdepåer av buprenorfin för behandling av opioidberoende i USA. I december 2018 erhöll Camurus amerikanska partner Braeburn ett tentativt godkännande från FDA för Brixadi (CAM2038) för behandling av opioidberoende.

Braeburn Pharmaceuticals Inc. and Camurus AB on Thursday, July 20 submitted their new drug application to the U.S. Food and Drug Administration for a long-acting opioid addiction treatment.

Tiberg, Camurus vd och forskningschef. Vi är oerhört tacksamma för alla de viktiga insatser som prövningsledare, sjukvårdspersonal och studiedeltagare liksom våra dedikerade team på Braeburn och Camurus bidragit med och som möjliggjort denna viktiga milstolpe i utvecklingen av ett nytt läkemedel mot opiatberoende. Camurus announces outcome of the arbitration process with Braeburn Thu, Dec 10, 2020 17:45 CET. Lund, Sweden — 10 December 2020 — Camurus AB (NASDAQ STO: CAMX) today announces that the ICC International Court of Arbitration has issued a partial award in the arbitration process between Camurus and Braeburn regarding the parties’ license agreement for the development and commercialization Camurus AB: Camurus announces that Braeburn receives Complete Response Letter for Brixadi for opioid use disorder in the US. Publicerad: 2020-12-02 (Cision) Camurus AB: Camurus meddelar att Braeburn erhåller Complete Response Letter för Brixadi i USA. Publicerad: 2020-12-02 (Cision) Camurus and Braeburn Pharmaceuticals announced that they have entered into an exclusive license agreement for the long-Camurus buprenorfinprodukt, CAM2038, for the treatment of opiate dependence and pain.

Camurus / Braeburn - Licensavtalet / Kickazz. 2020-12-30 10:09 IP: ItPAS77JZ. vad bolaget haft för intäkter tidigare spelar mindre roll. Det här är börsen och 

Camurus and Braeburn are planning for the receipt of approvals of CAM2038 for opioid use disorder in the US and Europe during the second half of 2018. Even though the marketing approval activities and clinical trials for CAM2038 are being carried out and paid for by Braeburn, Camurus has served Braeburn a material breach notice under the license agreement between the parties questioning Braeburn's performance in respect of its efforts, including to prepare for regulatory approval and commercialization of Brixadi™ for the treatment of opioid dependence in Canada and as a weekly extended release product in the US, and to develop and prepare for the Braeburn and Camurus will also seek to develop buprenorphine injection depot products for pain. Buprenorphine drug products have been demonstrated to be safe and effective in pain management. Lund, Sverige och Princeton, New Jersey — 2 maj 2017 — Camurus (NASDAQ STO: CAMX) och Braeburn Pharmaceuticals tillkännager idag positiva resultat från den nyligen avslutade fas 3-långtidsstudien av CAM2038 (vecko- och månadsdepåer av buprenorfin).Studieresultaten styrker produkternas säkerhet och behandlingseffekt i patienter med moderat till svårt opiatberoende. 2019-11-08 Camurus announces outcome of the arbitration process with Braeburn Thu, Dec 10, 2020 17:45 CET. Lund, Sweden — 10 December 2020 — Camurus AB (NASDAQ STO: CAMX) today announces that the ICC International Court of Arbitration has issued a partial award in the arbitration process between Camurus and Braeburn regarding the parties’ license agreement for the development and commercialization 2015-12-30 Braeburn Pharmaceuticals and Camurus enroll first patient in a phase 3 efficacy trial of long-acting treatment for opioid dependence; 2015-12-30 Change in the number of shares and votes in Camurus; 2015-12-15 Braeburn Pharmaceuticals and Camurus announce start of Phase 3 trial of long-acting buprenorphine treatments for opioid dependence Camurus Announces That FDA Grants Braeburn's Citizen Petition, Eliminating the Risk of Further Blocking of Brixadi™ From the US market PRESS RELEASE PR Newswire Nov. 7, 2019, 10:29 PM While our focus is opioid addiction, we are also exploring other therapeutic areas where our expertise and technology can benefit patients. View our pipeline.

2020-12-10 17:45:00 Camurus AB: Camurus announces outcome of the arbitration process with Braeburn -2,29% | 40,4 MSEK pdf  Lund – 10 december 2020 – Camurus AB (NASDAQ STO: CAMX) meddelar Arbitration har utfärdat deldom i skiljeförfarandet mellan Camurus och Braeburn  Nytt från koncernen: Camurus meddelar att Braeburn erhåller Complete Response Camurus utvecklar idag läkemedel för behanding av svåra och svåra  Camurus AB: Camurus meddelar att Braeburn erhåller Complete Response Letter för Brixadi i USA. 02 december 2020 kl 01:40.
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Amerikanska läkemedelsverket FDA begärde mer information från Camurus licenspartner Braeburn kring registeransökan för Brixadi. Aktien föll kraftigt, som mest 17 procent, men återhämtade sig något och stängde 12 procent ned.

Bakgrunden är ett ”väsentligt avtalsbrott mot parternas  Nov 1, 2017 (buprenorphine injectable) submitted by Braeburn Pharmaceuticals, Inc., for the treatment of opioid dependence. During this meeting  2016年11月14日 Braeburn Pharmaceuticals and Camurus Announce Positive Top-line Phase 3 Results for Long-acting Buprenorphine (CAM2038) for  Nov 2, 2017 Indivior could see competition to RBP-6000 quickly however, as Camurus and Braeburn Pharma's formulation of the drug (called CAM2038)  as Camurus/Braeburn Pharmaceuticals' CAM-2038, could, therefore, appeal to both payers and prescribers. Indeed, 86-96% of surveyed physicians are willing  Dec 10, 2018 Camurus (Lund, Sweden), a partner of Braeburn (Plymouth Meeting, PA), announced1 the positive opinion and recommendation by the  Jan 6, 2020 The company believed that the Camurus weekly and monthly depot injection products licensed by Braeburn would enable clinicians and  Apr 20, 2020 Helsinn Healthcare; Midatech/Galena Biopharma; Merck; Acacia Pharma; Cara Therapeutics; Camurus/Braeburn.
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Camurus and Braeburn Pharmaceuticals announced that they have entered into an exclusive license agreement for the long-Camurus buprenorfinprodukt, CAM2038, for the treatment of opiate dependence and pain. Braeburn receive exclusive licensing rights in North America and an option for Japan, Korea, Taiwan and China. Camurus retains all rights in the rest of the world. Under […]

Camurus and Braeburn are planning for the receipt of approvals of CAM2038 for opioid use disorder in the US and Europe during the second half of 2018. Even though the marketing approval activities and clinical trials for CAM2038 are being carried out and paid for by Braeburn, Camurus has served Braeburn a material breach notice under the license agreement between the parties questioning Braeburn's performance in respect of its efforts, including to prepare for regulatory approval and commercialization of Brixadi™ for the treatment of opioid dependence in Canada and as a weekly extended release product in the US, and to develop and prepare for the Braeburn and Camurus will also seek to develop buprenorphine injection depot products for pain. Buprenorphine drug products have been demonstrated to be safe and effective in pain management. Lund, Sverige och Princeton, New Jersey — 2 maj 2017 — Camurus (NASDAQ STO: CAMX) och Braeburn Pharmaceuticals tillkännager idag positiva resultat från den nyligen avslutade fas 3-långtidsstudien av CAM2038 (vecko- och månadsdepåer av buprenorfin).Studieresultaten styrker produkternas säkerhet och behandlingseffekt i patienter med moderat till svårt opiatberoende. 2019-11-08 Camurus announces outcome of the arbitration process with Braeburn Thu, Dec 10, 2020 17:45 CET. Lund, Sweden — 10 December 2020 — Camurus AB (NASDAQ STO: CAMX) today announces that the ICC International Court of Arbitration has issued a partial award in the arbitration process between Camurus and Braeburn regarding the parties’ license agreement for the development and commercialization 2015-12-30 Braeburn Pharmaceuticals and Camurus enroll first patient in a phase 3 efficacy trial of long-acting treatment for opioid dependence; 2015-12-30 Change in the number of shares and votes in Camurus; 2015-12-15 Braeburn Pharmaceuticals and Camurus announce start of Phase 3 trial of long-acting buprenorphine treatments for opioid dependence Camurus Announces That FDA Grants Braeburn's Citizen Petition, Eliminating the Risk of Further Blocking of Brixadi™ From the US market PRESS RELEASE PR Newswire Nov. 7, 2019, 10:29 PM While our focus is opioid addiction, we are also exploring other therapeutic areas where our expertise and technology can benefit patients.