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AVADEL PHARMACEUTICALS (AVDL)

Earnings summaries and quarterly performance for AVADEL PHARMACEUTICALS.

Recent press releases and 8-K filings for AVDL.

Avadel Pharmaceuticals Announces Increased Acquisition Offer from Alkermes
AVDL
M&A
Takeover Bid
  • Alkermes plc has increased its offer to acquire Avadel Pharmaceuticals plc to up to $22.50 per share, consisting of $21.00 in cash and one $1.50 contingent value right (CVR).
  • This represents an increase from the original offer of $18.50 in cash per share plus the $1.50 CVR.
  • The Increased Offer values Avadel at up to approximately $2.37 billion, assuming the CVR milestone is achieved.
  • The CVR is contingent upon final U.S. Food and Drug Administration (FDA) LUMRYZ™ Approval for idiopathic hypersomnia in adults by the end of 2028.
  • Avadel's board determined that Alkermes' Increased Offer is superior to an unsolicited proposal from H. Lundbeck A/S, leading to the amendment of the transaction agreement on November 18, 2025.
Nov 19, 2025, 11:23 AM
Avadel Pharmaceuticals plc Board Declares Lundbeck Proposal a Superior Offer
AVDL
M&A
Takeover Bid
  • Avadel Pharmaceuticals plc's Board of Directors has determined that an unsolicited proposal from H. Lundbeck A/S, received on November 13, 2025, constitutes a "Company Superior Proposal".
  • The Lundbeck Proposal values Avadel at up to $23.00 per ordinary share, implying a total equity value of approximately $2.4 billion. This offer includes $21.00 per share in cash at closing and a non-transferable contingent value right (CVR) for potential additional cash payments of up to $2.00 per share based on future net sales milestones.
  • This determination triggers a five business day period during which Avadel will discuss or negotiate with Alkermes plc regarding any proposal to amend their existing transaction agreement.
  • The Alkermes Transaction Agreement remains in full effect, and Avadel's Board has not changed its recommendation in support of the Alkermes acquisition at this time.
Nov 17, 2025, 11:02 AM
Avadel Pharmaceuticals Receives Unsolicited Acquisition Proposal from Lundbeck
AVDL
M&A
Takeover Bid
  • Avadel Pharmaceuticals plc received an unsolicited acquisition proposal from H. Lundbeck A/S for up to $23.00 per ordinary share, comprising $21.00 in cash at closing and a non-transferable contingent value right (CVR) for an additional $2.00 based on future sales milestones.
  • This new proposal compares to a definitive transaction agreement with Alkermes plc, announced on October 22, 2025, for up to $20.00 per ordinary share, including $18.50 in cash and a $1.50 CVR.
  • Avadel's Board of Directors has determined that the Lundbeck Proposal is reasonably expected to result in a "Company Superior Proposal", allowing for discussions and negotiations with Lundbeck, but has not yet changed its recommendation in favor of the Alkermes acquisition.
Nov 14, 2025, 11:03 AM
Avadel Pharmaceuticals Reports Strong Q3 2025 Results and Announces Acquisition by Alkermes
AVDL
Earnings
M&A
Legal Proceedings
  • Avadel Pharmaceuticals reported net product revenue of $77.5 million from LUMRYZ sales for the third quarter ended September 30, 2025, representing a 55% increase compared to the same period in 2024.
  • As of September 30, 2025, approximately 3,400 patients were being treated with LUMRYZ, a 48% increase compared to September 30, 2024.
  • The company announced a definitive agreement for Alkermes plc to acquire Avadel for total transaction consideration of up to $20.00 per share in cash, valuing Avadel at approximately $2.1 billion. The transaction is expected to close in the first quarter of 2026.
  • Avadel entered into a global settlement agreement with Jazz Pharmaceuticals, dismissing all litigation and allowing Avadel to commercialize LUMRYZ for indications beyond narcolepsy as soon as March 1, 2028.
  • For the quarter ended September 30, 2025, Avadel reported net income of $20 thousand, compared to a net loss of $2.6 million for the same period in 2024.
Nov 4, 2025, 9:08 PM
Avadel Pharmaceuticals plc to be Acquired by Alkermes plc
AVDL
M&A
Takeover Bid
Guidance Update
  • Alkermes plc has entered into a definitive agreement to acquire Avadel Pharmaceuticals plc for total consideration of up to $20.00 per share in cash, valuing the transaction at approximately $2.1 billion.
  • The acquisition price includes $18.50 per share in cash at closing and a Contingent Value Right (CVR) for an additional $1.50 per share, payable upon final FDA approval of LUMRYZ™ for idiopathic hypersomnia by the end of 2028.
  • This transaction represents a 38% premium to Avadel's weighted average trading price over the three months prior to October 22, 2025, and is expected to close in the first quarter of 2026.
  • The acquisition is anticipated to be immediately accretive to Alkermes, enhancing its revenue growth and profitability by adding Avadel's FDA-approved product, LUMRYZ™, to its commercial portfolio.
  • Avadel Pharmaceuticals plc expects net revenues for 2025 to be between $265 million and $275 million.
Oct 22, 2025, 1:29 PM
Avadel Pharmaceuticals and Jazz Pharmaceuticals Reach Global Settlement
AVDL
Legal Proceedings
New Projects/Investments
  • Avadel Pharmaceuticals plc and Jazz Pharmaceuticals Inc. have entered into a global settlement resolving all litigation between the companies, effective October 21, 2025.
  • As part of the agreement, Jazz will make a $90 million payment to Avadel and grant Avadel a perpetual, worldwide license for patents that could be asserted against LUMRYZ.
  • Avadel will pay Jazz ongoing royalties of 3.85% of net sales for LUMRYZ in narcolepsy and 10% of net sales for LUMRYZ in other indications (including idiopathic hypersomnia) through February 18, 2036, with royalties for narcolepsy sales starting October 1, 2025.
  • The settlement provides a pathway for LUMRYZ to be sold for future FDA-approved indications, such as idiopathic hypersomnia, beginning no earlier than March 1, 2028.
Oct 22, 2025, 10:40 AM
Avadel Pharmaceuticals Licenses Valiloxybate from XWPharma
AVDL
New Projects/Investments
  • Avadel Pharmaceuticals plc entered into an exclusive global license agreement with XWPharma Ltd. on August 29, 2025, for valiloxybate, a GABAB receptor agonist, for all indications including narcolepsy and idiopathic hypersomnia.
  • Valiloxybate is designed as a once-at-bedtime, salt-free, and artificial sweetener-free oxybate formulation, intended to expand Avadel's sleep medicine portfolio.
  • Under the terms of the agreement, Avadel will pay XWPharma an upfront payment of $20 million , potential development milestones of up to $30 million , and tiered sales milestones up to $155 million for annual net sales up to $750 million, with additional payments for higher sales.
  • Avadel also agreed to pay tiered royalties ranging from high-single digit to mid-teens as a percentage of annual net sales of the licensed products.
  • Initial pharmacokinetic studies for valiloxybate are expected to begin in the fourth quarter of 2025, with a pivotal PK trial planned for the second half of 2026.
Sep 3, 2025, 8:41 PM
Avadel Pharmaceuticals Q1 2025 Earnings, Guidance & Legal Update
AVDL
Earnings
Guidance Update
Legal Proceedings
Revenue Acceleration/Inflection
New Projects/Investments
  • Robust Q1 performance: Achieved net revenue of $52.5M with a 93-100% year-over-year increase driven by strong LUMRYZ sales
  • Revised FY25 guidance: Raised outlook to $255M–$265M in net revenue, with Q2 revenue expected at $60–$63M and cash flow guidance increased to $30–$40M
  • Favorable legal developments: On May 6, 2025, the Federal Circuit overturned key parts of the injunction, unlocking new clinical trials and enabling FDA pursuit of LUMRYZ approvals beyond narcolepsy, including idiopathic hypersomnia
  • Significant patient growth: Recorded a net addition of 300 patients, achieving 100% year-over-year growth and raising the therapy outlook to 3,400–3,600 by year-end
  • Robust clinical trial activity: Enrollment in the Phase 3 REVITALYZ trial remains strong with anticipated completion by Q4 2025 and top-line data expected in 1H25
  • Improved operational efficiency: Operating expenses decreased by 3%, supporting a move toward sustainable positive cash flow
May 7, 2025, 12:01 PM
Avadel Pharmaceuticals Updates at Virtual Healthcare Conference
AVDL
Guidance Update
Legal Proceedings
  • Avadel Pharmaceuticals presented its update at the Needham Virtual Healthcare Conference on April 8, 2025, highlighting improved patient demand metrics for LUMRYZ compared to Q4 2024.
  • The company reported that its REVITALYZ Phase 3 trial for LUMRYZ in Idiopathic Hypersomnia is on track to complete enrollment in the second half of 2025.
  • Avadel also noted that it has initiated four patent infringement lawsuits against Jazz Pharmaceuticals and anticipates generating sustainable positive cash flow in 2025.
Apr 8, 2025, 12:00 AM
Avadel Pharmaceuticals Special Call: LUMRYZ Commercial Strategy and Legal Developments
AVDL
Product Launch
Revenue Acceleration/Inflection
Legal Proceedings
  • LUMRYZ Launch and Clinical Value: The call focused on the commercial progress of LUMRYZ, Avadel’s once-at-bedtime oxybate therapy for narcolepsy, achieving rapid market adoption with over 2,500 net new patients within the first 18 months since approval.
  • Expanded Commercial Efforts: The company detailed strategic investments including an increased sales force, enhanced field and patient support teams, and direct-to-patient initiatives aimed at driving quarter-over-quarter revenue growth with a forecast of approximately 50% revenue growth in 2025 vs. 2024.
  • Patient Mix Optimization: Emphasis was placed on balancing the mix between switch patients (from first-generation oxybates) and new-to-oxybate patients to improve patient persistency and treatment outcomes, with recent trends showing around 60% new patients in the latter half of 2024.
  • Litigation and Future Indications: The executives addressed ongoing legal proceedings regarding the idiopathic hypersomnia injunction, expecting a decision in Q2, while affirming plans to expand LUMRYZ’s indications through new clinical studies and FDA submissions.
Mar 17, 2025, 12:31 PM