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Avadel Pharmaceuticals plc Ordinary Share - AVDL STOCK NEWS

Welcome to our dedicated page for Avadel Pharmaceuticals plc Ordinary Share news (Ticker: AVDL), a resource for investors and traders seeking the latest updates and insights on Avadel Pharmaceuticals plc Ordinary Share stock.

Avadel Pharmaceuticals plc (Nasdaq: AVDL) is a specialty pharmaceutical company headquartered in Dublin, Ireland, with operations in St. Louis, Missouri, and Lyon, France. The company focuses on developing, identifying, and commercializing differentiated pharmaceutical products designed to be safe, effective, and easy to administer, thereby improving patient adherence and outcomes. Avadel's products primarily target the urology, central nervous system (CNS) / sleep, and hospital markets.

One of Avadel's flagship products is LUMRYZ™, an extended-release formulation of sodium oxybate, approved by the U.S. Food & Drug Administration (FDA) for the treatment of cataplexy or excessive daytime sleepiness (EDS) in adults with narcolepsy. LUMRYZ is notable for its once-at-bedtime dosing, which eliminates the need for a middle-of-the-night dose, making it more convenient for patients.

The FDA granted LUMRYZ seven years of Orphan Drug Exclusivity, recognizing it as a major contribution to patient care over existing therapies. The approval was supported by results from the REST-ON trial, a Phase 3 study that demonstrated significant improvements in EDS, the Clinician Global Impression of Improvement (CGI-I), and reduced the frequency of cataplexy attacks.

Avadel recently announced its financial results for the third quarter ended September 30, 2023, reporting $7.0 million in net product revenue from LUMRYZ sales. The company has seen robust demand and positive feedback from the narcolepsy community, healthcare providers, and payers. Notably, CVS Health has moved LUMRYZ to preferred status starting January 1, 2024. Avadel also filed a supplemental NDA to extend LUMRYZ's indication to pediatric patients with narcolepsy, further expanding its market reach.

Financially, Avadel reported a net loss of $36.3 million for the quarter, driven by higher selling, general, and administrative expenses related to the LUMRYZ launch. Despite these challenges, the company maintains a strong cash position of $153.2 million as of September 30, 2023.

Looking ahead, Avadel plans to issue its Annual Report on Form 10-K for the year ended December 31, 2023, on February 29, 2024. The company continues to focus on expanding its product pipeline, including initiating a Phase 3 trial for idiopathic hypersomnia and optimizing commercial execution for LUMRYZ.

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Avadel Pharmaceuticals announces new data supporting the clinical profile of LUMRYZ for narcolepsy treatment
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Avadel Pharmaceuticals to participate in fireside chat at Jefferies Biotech CNS/Neuro Summit
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Avadel Pharmaceuticals plc to participate in investor conferences
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Avadel Pharmaceuticals plc (AVDL) Announces U.S. Commercial Launch of LUMRYZ™ and FDA Approval
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Avadel Pharmaceuticals plc (Nasdaq: AVDL) approved the grant of non-statutory options to three new employees to purchase 26,000 ordinary shares under Avadel’s 2021 Inducement Plan. The options have a ten-year term and vest over four years, with 25% vesting on the one-year anniversary of the grant date and 25% on each anniversary thereafter.
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FAQ

What is the current stock price of Avadel Pharmaceuticals plc Ordinary Share (AVDL)?

The current stock price of Avadel Pharmaceuticals plc Ordinary Share (AVDL) is $10.14 as of December 23, 2024.

What is the market cap of Avadel Pharmaceuticals plc Ordinary Share (AVDL)?

The market cap of Avadel Pharmaceuticals plc Ordinary Share (AVDL) is approximately 971.3M.

What is Avadel Pharmaceuticals plc?

Avadel Pharmaceuticals plc (Nasdaq: AVDL) is a specialty pharmaceutical company focused on developing differentiated pharmaceutical products for urology, CNS/sleep, and hospital markets.

What is LUMRYZ?

LUMRYZ is an extended-release formulation of sodium oxybate, approved by the FDA for treating cataplexy or excessive daytime sleepiness (EDS) in adults with narcolepsy. It is taken once at bedtime.

Where is Avadel Pharmaceuticals headquartered?

Avadel Pharmaceuticals is headquartered in Dublin, Ireland, with additional operations in St. Louis, Missouri, and Lyon, France.

What recent financial results did Avadel report?

For the third quarter ended September 30, 2023, Avadel reported $7.0 million in net product revenue from LUMRYZ sales and a net loss of $36.3 million.

What distinguishes LUMRYZ from other treatments?

LUMRYZ is the first and only once-at-bedtime oxybate treatment for narcolepsy, offering a more convenient dosing regimen compared to twice-nightly oxybate products.

What are the most common side effects of LUMRYZ?

The most common side effects include nausea, dizziness, bedwetting, headache, and vomiting.

What is the significance of LUMRYZ's Orphan Drug Exclusivity?

The FDA granted LUMRYZ seven years of Orphan Drug Exclusivity due to its significant contribution to patient care, providing a once-nightly dosing alternative to existing treatments.

How did the narcolepsy community respond to the launch of LUMRYZ?

The launch received overwhelmingly positive feedback, with early patient demand and significant support from healthcare providers and payers.

What other areas does Avadel Pharmaceuticals focus on?

In addition to narcolepsy, Avadel focuses on developing treatments for urology and hospital markets.

What are Avadel’s future plans for LUMRYZ?

Avadel plans to expand LUMRYZ's indication to pediatric patients and continue its Phase 3 trials for idiopathic hypersomnia.

Avadel Pharmaceuticals plc Ordinary Share

Nasdaq:AVDL

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971.33M
91.76M
4.77%
80.29%
9.15%
Drug Manufacturers - Specialty & Generic
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