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NASDAQ:AVDL

Avadel Pharmaceuticals Q3 2025 Earnings Report

Avadel Pharmaceuticals EPS Results

Actual EPS
$0.00
Consensus EPS
$0.04
Beat/Miss
Missed by -$0.04
One Year Ago EPS
-$0.03

Avadel Pharmaceuticals Revenue Results

Actual Revenue
$77.47 million
Expected Revenue
$78.05 million
Beat/Miss
Missed by -$585.00 thousand
YoY Revenue Growth
+55.00%

Avadel Pharmaceuticals Announcement Details

Quarter
Q3 2025
Time
Before Market Opens
Conference Call Date
Tuesday, November 4, 2025
Conference Call Time
4:00PM ET

Avadel Pharmaceuticals Earnings Headlines

Form 8.3 - Avadel Pharmaceuticals plc
Form 8.3 -Avadel Pharmaceuticals plc
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Form 8.3 -Avadel Pharmaceuticals plc
Form 8.3 -Avadel Pharmaceuticals plc
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About Avadel Pharmaceuticals

Avadel Pharmaceuticals (NASDAQ:AVDL) plc is a global specialty biopharmaceutical company focused on developing and delivering treatments for rare diseases and central nervous system disorders. Headquartered in Dublin, Ireland, with operations in the United States, Avadel’s portfolio centers on sleep disorder therapeutics, including its flagship low-sodium oxybate product, XYWAV, which is approved in the U.S. for the treatment of cataplexy or excessive daytime sleepiness in patients with narcolepsy. The company is also advancing FT218, a once-nightly formulation of sodium oxybate, currently under regulatory review for narcolepsy management.

Formed through a rebranding of Flamel Technologies in 2016 and a strategic shift toward rare disease drug development, Avadel has built its R&D capabilities around improving patient compliance and reducing daily sodium exposure compared to traditional therapies. Its clinical pipeline spans multiple indications within sleep medicine, aiming to address unmet needs such as idiopathic hypersomnia and other central nervous system conditions.

Avadel conducts its research and commercialization activities primarily in North America and Europe, leveraging a network of partnerships and specialty distributors to bring its therapies to patients. The company’s manufacturing sites are strategically located to support both clinical supply and commercial production, and it operates under the regulatory standards set by the U.S. Food and Drug Administration and the European Medicines Agency.

Through collaborations with academic centers, patient advocacy groups, and contract research organizations, Avadel continues to expand its expertise in orphan drug development. The company’s leadership team comprises seasoned pharmaceutical executives and scientists dedicated to advancing therapeutic solutions that improve quality of life for patients with rare and complex disorders.

View Avadel Pharmaceuticals Profile