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Avadel Pharmaceuticals to Provide a Corporate Update and Report Third Quarter 2024 Financial Results on November 12

Avadel Pharmaceuticals to Provide a Corporate Update and Report Third Quarter 2024 Financial Results on November 12

avadel pharmaceuticals将于11月12日提供公司更新并报告2024年第三季度财务业绩
GlobeNewswire ·  2024/11/04 21:00

DUBLIN, Nov. 04, 2024 (GLOBE NEWSWIRE) -- Avadel Pharmaceuticals plc (Nasdaq: AVDL), a biopharmaceutical company focused on transforming medicines to transform lives, announced today that it will host a conference call and live webcast at 8:30 a.m. ET on Tuesday, November 12, 2024, to provide a corporate update and discuss the Company's financial results for the third quarter ended September 30, 2024.

都柏林,2024年11月04日(环球新闻)-- Avadel Pharmaceuticals plc(纳斯达克:AVDL)是一家专注于转变药物以改变生命的生物制药公司,今天宣布将于2024年11月12日星期二东部时间上午8:30举行电话会议和现场直播,以提供企业更新并讨论截至2024年9月30日的第三季度财务业绩。

To access the conference call, investors are invited to dial (800) 579-2543 (U.S. and International) and reference the conference ID AVADEL. A live audio webcast of the call be accessed by visiting the investor relations section of the Company's website, . A replay of the webcast will be archived on Avadel's website for 90 days following the event.

要参加电话会议,投资者可拨打(800)579-2543(美国及国际)并引用会议ID AVADEL。可以通过访问公司网站的投资者关系部分来访问电话的直播音频网络广播。网络广播的回放将在活动结束后存档在Avadel的网站上,保存90天。

About Avadel Pharmaceuticals plc
Avadel Pharmaceuticals plc (Nasdaq: AVDL) is a biopharmaceutical company focused on transforming medicines to transform lives. Our approach includes applying innovative solutions to the development of medications that address the challenges patients face with current treatment options. Avadel's commercial product, LUMRYZ, was approved by the U.S. Food & Drug Administration (FDA) as the first and only once-at-bedtime oxybate for the treatment of cataplexy or excessive daytime sleepiness (EDS) in patients seven years and older with narcolepsy. For more information, please visit .

关于Avadel Pharmaceuticals,plc
Avadel Pharmaceuticals plc(纳斯达克:AVDL)是一家专注于转变药物以改变生命的生物制药公司。我们的方法包括应用创新解决方案来开发应对患者在当前治疗选择中面临挑战的药物。Avadel的商业产品LUMRYZ已被美国食品和药物管理局(FDA)批准为治疗发作性肌无力或过度白天嗜睡(EDS)的患者的首个也是唯一的睡前一次性羟基丁酸盐,适用于七岁及以上的发作性睡病患者。有关更多信息,请访问。

Investor Contact:
Courtney Mogerley
Precision AQ
Courtney.Mogerley@precisionAQ.com
(212) 698-8687

投资者联系人:
考特尼·莫杰利
精准AQ
Courtney.Mogerley@precisionAQ.com
(212) 698-8687

Media Contact:
Lesley Stanley
Real Chemistry
lestanley@realchemistry.com
(609) 273-3162

媒体联系人:
莱斯利·斯坦利
真实化学
lestanley@realchemistry.com
(609) 273-3162


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