Supernus Pharmaceuticals Completes Acquisition of Sage Therapeutics
Supernus Pharmaceuticals (Nasdaq: SUPN) has completed its acquisition of Sage Therapeutics, strengthening its position in neuropsychiatric treatments. The deal includes ´Ü±«¸é´Ü±«³Õ´¡·¡Â®, the first FDA-approved oral medicine for postpartum depression, and a CNS discovery platform.
The transaction structure includes $8.50 per share in cash plus contingent value rights (CVRs) worth up to $3.50 per share tied to specific milestones. The acquisition garnered 58% shareholder approval with 36,313,509 shares tendered. Supernus expects annual cost synergies of up to $200 million and projects the acquisition to be accretive by 2026.
The deal adds collaboration revenue from ZURZUVAE (50% of U.S. net sales through Biogen partnership) and complements Supernus' existing portfolio including Qelbree®, ONAPGO�, and GOCOVRI®.
Supernus Pharmaceuticals (Nasdaq: SUPN) ha completato l'acquisizione di Sage Therapeutics, rafforzando la sua posizione nel settore dei trattamenti neuropsichiatrici. L'accordo include ´Ü±«¸é´Ü±«³Õ´¡·¡Â®, il primo farmaco orale approvato dalla FDA per la depressione postpartum, e una piattaforma di scoperta nel sistema nervoso centrale.
La struttura della transazione prevede 8,50 dollari per azione in contanti più diritti di valore contingente (CVR) fino a 3,50 dollari per azione legati a specifici obiettivi. L'acquisizione ha ottenuto il 58% di approvazione da parte degli azionisti con 36.313.509 azioni presentate. Supernus prevede sinergie di costo annuali fino a 200 milioni di dollari e stima che l'acquisizione sarà accrescitiva entro il 2026.
L'accordo aggiunge ricavi da collaborazioni derivanti da ZURZUVAE (50% delle vendite nette negli USA tramite la partnership con Biogen) e completa il portafoglio esistente di Supernus, che comprende Qelbree®, ONAPGO� e GOCOVRI®.
Supernus Pharmaceuticals (Nasdaq: SUPN) ha completado la adquisición de Sage Therapeutics, fortaleciendo su posición en tratamientos neuropsiquiátricos. El acuerdo incluye ´Ü±«¸é´Ü±«³Õ´¡·¡Â®, el primer medicamento oral aprobado por la FDA para la depresión posparto, y una plataforma de descubrimiento del sistema nervioso central.
La estructura de la transacción contempla 8,50 dólares por acción en efectivo más derechos de valor contingente (CVR) por hasta 3,50 dólares por acción vinculados a hitos especÃficos. La adquisición obtuvo el 58% de aprobación de los accionistas con 36.313.509 acciones entregadas. Supernus espera sinergias de costos anuales de hasta 200 millones de dólares y proyecta que la adquisición será accretiva para 2026.
El acuerdo añade ingresos por colaboraciones de ZURZUVAE (50% de las ventas netas en EE.UU. a través de la asociación con Biogen) y complementa el portafolio existente de Supernus, que incluye Qelbree®, ONAPGO� y GOCOVRI®.
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거래 구조ëŠ� 주당 현금 8.50달러와 íŠ¹ì • 마ì¼ìŠ¤í†¤ì—� ì—°ë™ë� 최대 주당 3.50달러 ìƒë‹¹ì� ì¡°ê±´ë¶€ ê°¶Äì¹� 권리(CVR)ë¥� í¬í•¨í•©ë‹ˆë‹�. ì¸ìˆ˜ëŠ� 주주 58%ì� 승ì¸ì� 받았으며 36,313,509주갶� ì œì¶œë˜ì—ˆìŠµë‹ˆë‹�. 슈í¼ë„ˆìФëŠ� ì—°ê°„ 최대 2ì–� 달러ì� 비용 시너지 효과ë¥� 기대하며 2026년까지 ì¸ìˆ˜ê°¶Ä 수ìµì„±ì— ê¸ì •ì ì¼ ê²ƒìœ¼ë¡� ì „ë§í•©ë‹ˆë‹�.
ì´ë²ˆ 거래ë¡� ZURZUVAE(ë°”ì´ì˜¤ì ê³¼ì˜ íŒŒíŠ¸ë„ˆì‹ì� 통한 ë¯¸êµ ìˆœë§¤ì¶œì˜ 50%)로부í„� í˜‘ë ¥ 수ìµì� 추갶Äë˜ë©�, 슈í¼ë„ˆìФì� 기존 í¬íЏí´ë¦¬ì˜¤ì¸ Qelbree®, ONAPGOâ„�, GOCOVRI®ë¥� 보완합니ë‹�.
Supernus Pharmaceuticals (Nasdaq : SUPN) a finalisé l'acquisition de Sage Therapeutics, renforçant ainsi sa position dans les traitements neuropsychiatriques. L'accord inclut ´Ü±«¸é´Ü±«³Õ´¡·¡Â®, le premier médicament oral approuvé par la FDA pour la dépression post-partum, ainsi qu'une plateforme de découverte du système nerveux central.
La structure de la transaction comprend 8,50 $ par action en espèces ainsi que des droits de valeur contingente (CVR) pouvant atteindre 3,50 $ par action liés à des jalons spécifiques. L'acquisition a obtenu 58 % d'approbation des actionnaires avec 36 313 509 actions déposées. Supernus prévoit des synergies de coûts annuelles pouvant atteindre 200 millions de dollars et estime que l'acquisition sera créatrice de valeur d'ici 2026.
L'accord apporte des revenus de collaboration issus de ZURZUVAE (50 % des ventes nettes aux États-Unis via le partenariat avec Biogen) et complète le portefeuille existant de Supernus, comprenant Qelbree®, ONAPGO� et GOCOVRI®.
Supernus Pharmaceuticals (Nasdaq: SUPN) hat die Übernahme von Sage Therapeutics abgeschlossen und stärkt damit seine Position im Bereich neuropsychiatrischer Behandlungen. Der Deal umfasst ´Ü±«¸é´Ü±«³Õ´¡·¡Â®, das erste von der FDA zugelassene orale Medikament gegen postpartale Depression, sowie eine CNS-Entdeckungsplattform.
Die Transaktionsstruktur sieht 8,50 USD pro Aktie in bar sowie bedingte Wertrechte (CVRs) im Wert von bis zu 3,50 USD pro Aktie vor, die an bestimmte Meilensteine gekoppelt sind. Die Übernahme erhielt 58 % Zustimmung der Aktionäre mit 36.313.509 eingereichten Aktien. Supernus erwartet jährliche Kostensynergien von bis zu 200 Millionen USD und prognostiziert, dass die Übernahme ab 2026 ertragssteigernd sein wird.
Der Deal bringt Kollaborationsumsätze aus ZURZUVAE (50 % der US-Nettoverkäufe durch die Partnerschaft mit Biogen) und ergänzt das bestehende Portfolio von Supernus, zu dem Qelbree®, ONAPGO� und GOCOVRI® gehören.
- Expected cost synergies of up to $200 million annually
- Acquisition projected to be accretive by 2026
- Adds fourth growth product to portfolio with ZURZUVAE
- Gains 50% revenue share from ZURZUVAE U.S. sales through Biogen collaboration
- Strengthens CNS discovery platform and expertise
- Diversifies revenue streams with first-in-class postpartum depression treatment
- Significant upfront cash payment of $8.50 per share required
- CVR payments of up to $3.50 per share may be required if milestones are met
- Integration risks with existing operations
- ZURZUVAE sales milestones are challenging: requires up to $375M in U.S. sales by 2030
Insights
Supernus strengthens its CNS portfolio through Sage acquisition, gaining ZURZUVAE and potential $200M annual synergies; accretive by 2026.
Supernus Pharmaceuticals' completed acquisition of Sage Therapeutics represents a strategic expansion of its neuropsychiatry portfolio with significant long-term growth implications. The deal's structure�
The acquisition's cornerstone is ZURZUVAE (zuranolone), the first FDA-approved oral treatment for postpartum depression. This adds a fourth growth product to Supernus' portfolio alongside Qelbree, ONAPGO, and GOCOVRI. What makes this particularly valuable is the revenue-sharing structure with Biogen, where Supernus receives
The projected
Beyond ZURZUVAE, Supernus gains Sage's CNS discovery platforms, augmenting its research capabilities in a therapeutic area where innovation is challenging but highly rewarded. The
Acquisition strengthens Supernusâ€� leading presence in neuropsychiatric conditions with an innovative commercial product, ´Ü±«¸é´Ü±«³Õ´¡·¡Â® (zuranolone), and a novel CNS discovery platform, accelerating mid- to long-term revenue and cash flow growth and further diversifying revenue base
ROCKVILLE, Md., July 31, 2025 (GLOBE NEWSWIRE) -- Supernus Pharmaceuticals, Inc. (Nasdaq: SUPN) (“Supernus�) today announced that it has successfully completed its previously announced acquisition of Sage Therapeutics, Inc. (Nasdaq: SAGE) (“Sage�).
“Sage is an ideal fit in our corporate development strategy, adding a significant fourth growth product to our portfolio and further diversifying our sources of future revenue,� said Jack Khattar, President and CEO of Supernus Pharmaceuticals. “With our proven track record of strong commercial execution along with the expected cost synergies, the acquisition is expected to be accretive in 2026.�
Compelling Strategic Rationale
- Strengthens psychiatry portfolio with ZURZUVAE® (zuranolone) capsules CIV, the first and only FDA-approved oral medicine indicated for the treatment of postpartum depression in adults.
- Diversifies and increases revenue base and cash flow:
- Addition of collaboration revenue from net sales of ZURZUVAE (
50% of total net revenue Biogen, Inc. records for ZURZUVAE in the U.S. pursuant to a collaboration agreement), and - Combined with its three other growth products (Qelbree®, ONAPGO�, and GOCOVRI®), Supernus believes it is poised for significant future growth.
- Addition of collaboration revenue from net sales of ZURZUVAE (
- Augments Supernus central nervous system discovery platforms and expertise.
- Strong fit with existing Supernus infrastructure is expected to result in cost synergies of up to
$200 million on an annual basis. - The acquisition is expected to be accretive in 2026.
The Offer and the Merger
The Offer and withdrawal rights for all outstanding shares of common stock, par value
Each CVR paid to Sage stockholders represents a non-transferable and non-tradable contractual contingent right to receive a cash payment of up to
One milestone payment of
A second milestone payment of
A third milestone payment of
A fourth milestone payment of
Each milestone may only be achieved once. The maximum amount payable with respect to the CVR issued in respect to each Share is
Equiniti Trust Company, LLC, the depositary for the Offer, has advised Supernus that a total of 36,313,509 Shares were validly tendered and not validly withdrawn in the Offer, representing approximately 58 percent of the Shares outstanding.
All of the conditions of the Offer have been satisfied, and effective as of the Expiration Time, Supernus and its wholly owned subsidiary, Saphire, Inc. (“Purchaser�), accepted for payment all Shares that were validly tendered and not validly withdrawn in the Offer, and will as promptly as practicable thereafter pay for all such validly tendered Shares. Following the completion of the Offer, Supernus completed the acquisition of Sage through the merger of Purchaser with and into Sage, without a vote of Sage stockholders in accordance with Section 251(h) of the General Corporation Law of the State of Delaware (“DGCL�), with Sage surviving the merger as a wholly owned subsidiary of Supernus. In connection with the merger, each Share not previously purchased in the Offer (other than (i) Shares held by Sage (or held in Sage’s treasury) immediately prior to the effective time of the merger, (ii) any Shares held by Supernus or Purchaser or any direct or indirect wholly owned subsidiary of Supernus or Purchaser immediately prior to the effective time of the merger, or (iii) Shares held by any stockholder who was entitled to appraisal rights under Section 262 of the DGCL and properly exercised and perfected their respective demands for appraisal of such Shares pursuant to Section 262 of the DGCL and, as of the effective time of the merger, has neither effectively withdrawn nor lost their rights to such appraisal and payment under the DGCL with respect to such Shares) was converted into the right to receive the Offer Price, less any applicable withholding taxes and without interest. The Shares will be delisted from the Nasdaq Global Market.
Advisors
Moelis & Company LLC acted as the exclusive financial advisor to Supernus. Goldman Sachs & Co. LLC acted as the exclusive financial advisor to Sage. Saul Ewing LLP served as legal counsel to Supernus. Kirkland & Ellis LLP served as legal counsel to Sage.
About Supernus Pharmaceuticals, Inc.
Supernus Pharmaceuticals (the Company) is a biopharmaceutical company focused on developing and commercializing products for the treatment of central nervous system (CNS) diseases.
Our diverse neuroscience portfolio includes approved treatments for attention-deficit hyperactivity disorder (ADHD), dyskinesia in Parkinson’s disease (PD) patients receiving levodopa-based therapy, hypomobility in PD, postpartum depression (PPD), epilepsy, migraine, cervical dystonia, and chronic sialorrhea. We are developing a broad range of novel product candidates for CNS disorders.
For more information, please visit .
Forward-Looking Statements
This press release includes forward-looking statements. These statements do not convey historical information but relate to predicted or potential future events that are based upon management's current expectations. These statements are subject to risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. In addition to the factors mentioned in this press release, such risks and uncertainties include, but are not limited to, the Company’s ability to sustain and increase its profitability; the Company’s ability to raise sufficient capital to fully implement its corporate strategy; the implementation of the Company’s corporate strategy; the Company’s future financial performance and projected expenditures; the Company’s ability to increase the number of prescriptions written for each of its products, the products of its subsidiaries and products acquired through the acquisition of Sage; the Company’s ability to increase its net revenue from its products, the products of its subsidiaries and products acquired through the acquisition of Sage; the Company’s ability to commercialize its products, the products of its subsidiaries and products acquired through the acquisition of Sage; the Company’s ability to enter into future collaborations with pharmaceutical companies and academic institutions or to obtain funding from government agencies; the Company’s product research and development activities, including the timing and progress of the Company’s clinical trials, and projected expenditures; the Company’s ability to receive, and the timing of any receipt of, regulatory approvals to develop and commercialize the Company’s product candidates; the Company’s ability to protect its intellectual property and the intellectual property of its subsidiaries and operate its business without infringing upon the intellectual property rights of others; the Company’s expectations regarding federal, state and foreign regulatory requirements; the therapeutic benefits, effectiveness and safety of the Company’s product candidates; the accuracy of the Company’s estimates of the size and characteristics of the markets that may be addressed by its product candidates; the Company’s ability to increase its manufacturing capabilities for its products and product candidates; the Company’s projected markets and growth in markets; the Company’s product formulations and patient needs and potential funding sources; the Company’s staffing needs; and other risk factors set forth from time to time in the Company’s filings with the Securities and Exchange Commission made pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934, as amended. The Company undertakes no obligation to update the information in this press release to reflect events or circumstances after the date hereof or to reflect the occurrence of anticipated or unanticipated events.
CONTACTS:
Jack A. Khattar, President and CEO
Timothy C. Dec, Senior Vice President and CFO
Supernus Pharmaceuticals, Inc.
(301) 838-2591
INVESTOR CONTACT:
Peter Vozzo
ICR Healthcare
(443) 213-0505
