Sage Therapeutics, Inc. (SAGE) Bundle
Given the pending acquisition by Supernus Pharmaceuticals for up to approximately $795 million, is Sage Therapeutics, Inc. (SAGE) a biotech story about a successful exit, or a blueprint for how to monetize novel brain health medicines? Your answer hinges on understanding how a company with a TTM revenue of only $70.4 million as of mid-2025 can command a $549 million market capitalization, a valuation driven by its distinctive offerings like ZURZUVAE, the first-and-only oral treatment for postpartum depression (PPD). We need to look past the Q1 2025 net loss of $62.2 million and analyze the core mission, the proprietary science targeting GABA and NMDA receptor systems, and the commercial strategy that saw ZURZUVAE collaboration revenue jump 68% in Q2 2025.
Sage Therapeutics, Inc. (SAGE) History
You need to understand the history of Sage Therapeutics, Inc. to grasp its current valuation and future trajectory, especially after the major shift in 2025. This is a company that started with a bold, singular focus on brain health and went from a $35 million seed round to a major acquisition in just over a decade. The story is one of high-risk, high-reward biopharma development.
Given Company's Founding Timeline
Year established
Sage Therapeutics was established in 2010, incorporated in Delaware, with a mission to develop innovative medicines for brain health disorders.
Original location
The company was originally based in Cambridge, Massachusetts, a hub for biopharmaceutical research.
Founding team members
The core founding team included Steven Paul, M.D., Douglas Feltner, M.D., and Mark Galli. Their vision was to target the central nervous system (CNS) with novel compounds, moving beyond traditional psychiatric treatments.
Initial capital/funding
The initial capital came from a Series A financing round completed in 2011, securing $35 million in funding. This capital was foundational for advancing their early-stage research and development pipeline.
Given Company's Evolution Milestones
| Year | Key Event | Significance |
|---|---|---|
| 2014 | Initial Public Offering (IPO) | Raised $108 million, providing substantial capital to accelerate clinical development programs. |
| 2019 | FDA Approval of Zulresso (brexanolone) | First-ever FDA-approved treatment specifically for postpartum depression (PPD), validating their core scientific platform. |
| 2020 | Strategic Collaboration with Biogen | Secured a massive partnership, including an upfront payment, equity investment, and potential milestones totaling up to $3 billion, significantly bolstering their financial stability and commercial reach. |
| 2023 | FDA Approval of ZURZUVAE (zuranolone) | Approved as the first and only oral treatment for PPD, a key commercial differentiator from the IV-infusion Zulresso. |
| 2025 | Acquisition by Supernus Pharmaceuticals | Completed in July 2025, this transaction marked the end of Sage Therapeutics as an independent public entity, shifting its assets and pipeline into a larger neuropsychiatric portfolio. |
Given Company's Transformative Moments
The company's journey was defintely defined by a few pivotal, high-stakes decisions that completely reshaped its financial and strategic profile. You can trace the company's evolution through its focus on the GABA-A receptor system for brain health disorders.
The first major pivot was committing to Postpartum Depression (PPD) as a lead indication. This focus led to two first-in-class treatments, Zulresso and ZURZUVAE, establishing Sage Therapeutics as a leader in an area of high unmet medical need. The market for ZURZUVAE, the oral therapy, showed promising early traction in 2025, with Q2 collaboration revenue hitting $23.2 million, a 68% increase from Q1 2025.
The 2020 collaboration with Biogen was a critical financial lifeline and validation, injecting billions in potential capital. But, as often happens in biopharma, the biggest change came from a strategic exit. The most recent and transformative moment was the acquisition by Supernus Pharmaceuticals, Inc., completed in July 2025. This move valued each common share at $8.50 cash plus a non-transferable Contingent Value Right (CVR), effectively taking the company private under a new owner.
- The Biogen Deal: Provided the capital runway, which was critical as the company was still burning cash, reporting a net loss of $62.2 million in Q1 2025.
- Pipeline Prioritization: In late 2024 and early 2025, the company strategically reduced research and development (R&D) expenses, focusing resources on the most promising candidates like SAGE-319 for neurodevelopmental disorders. This was a necessary step to manage cash burn.
- The Supernus Acquisition: This event, finalized in mid-2025, was the ultimate transformative decision. It provided immediate, guaranteed value to shareholders and integrated Sage Therapeutics' key assets, particularly ZURZUVAE, into a larger commercial infrastructure.
To fully appreciate the financial implications of these shifts, you should review the detailed financial performance. Breaking Down Sage Therapeutics, Inc. (SAGE) Financial Health: Key Insights for Investors
Sage Therapeutics, Inc. (SAGE) Ownership Structure
Sage Therapeutics, Inc. is a publicly-traded biopharmaceutical company, and its ownership structure is heavily weighted toward institutional investors, which is typical for a company in the high-risk, high-reward biotech sector.
This high institutional concentration means the company's strategic direction is largely influenced by large financial firms, not individual retail traders. For a deeper dive into the company's financial health, you can check out Breaking Down Sage Therapeutics, Inc. (SAGE) Financial Health: Key Insights for Investors.
Given Company's Current Status
Sage Therapeutics, Inc. is a Publicly Held company, trading on the NASDAQ Global Market under the ticker symbol SAGE. As of November 2025, the company's market capitalization stood at approximately $549 million. Its stock price as of July 23, 2025, was $8.77 per share. The company's focus on brain health medicines, like its FDA-approved postpartum depression treatment ZURZUVAE, positions it in a volatile but potentially high-growth segment of the pharmaceutical industry.
The company had approximately 62.61 million shares outstanding as of June 2025.
Given Company's Ownership Breakdown
The ownership breakdown, calculated against the total shares outstanding as of mid-2025, shows a clear dominance by institutional money. This is defintely a key factor to watch, as large institutional holders can quickly shift sentiment and stock price with major block trades.
| Shareholder Type | Ownership, % | Notes |
|---|---|---|
| Institutional Investors | 48.70% | Holdings by mutual funds, hedge funds, and pension funds like Vanguard and State Street Corp. |
| Public/Retail Investors | 31.81% | Shares held by the general public and smaller individual accounts. |
| Insiders (Executives & Directors) | 19.49% | Shares held by the leadership team and board members. |
Given Company's Leadership
The company is steered by a seasoned executive team with deep experience in the biopharmaceutical space. The current leadership is focused on commercializing ZURZUVAE and advancing the rest of the clinical pipeline, especially in neurology and neuropsychiatry.
- Barry Greene: Chief Executive Officer (CEO) and Member of the Board of Directors. He joined in 2020 and brings over 30 years of biopharmaceutical industry experience.
- Geno Germano: Chairman of the Board. He has held this role since January 2024.
- Chris Benecchi: Chief Operating Officer (COO). He took on this role in October 2024, overseeing commercial operations and corporate strategy.
- Mike Quirk, Ph.D.: Chief Scientific Officer and Interim Head of R&D. He assumed key R&D responsibilities in March 2025 following a leadership transition.
- Kimi Iguchi: Chief Financial Officer (CFO).
- Gregory Shiferman: Senior Vice President, General Counsel. He has been in this role since November 2024.
The leadership's primary near-term action is driving significant topline revenue growth for 2025, with ZURZUVAE revenue reaching $13.8 million in the first quarter of 2025 alone.
Sage Therapeutics, Inc. (SAGE) Mission and Values
Sage Therapeutics, Inc. (SAGE) is fundamentally driven by a mission to transform brain health, aiming for a world where people can live the lives they imagine by pioneering new medicines. This purpose goes beyond profit, focusing on patient impact, which is especially critical given the company's Q2 2025 net loss of $49.7 million as it invests heavily in commercializing treatments like ZURZUVAE.
You're looking at a biopharmaceutical company that's trying to change the standard of care for serious conditions like postpartum depression (PPD). Their core purpose, therefore, is rooted in scientific courage and a deep commitment to the patient community, not just revenue growth, which hit $23.2 million in collaboration revenue for ZURZUVAE in Q2 2025. You defintely need to see the values that underpin that kind of investment. Breaking Down Sage Therapeutics, Inc. (SAGE) Financial Health: Key Insights for Investors
Given Company's Core Purpose
The company's cultural DNA is built on five core values that guide their research and commercialization efforts, particularly as they focus on establishing ZURZUVAE as a first-line therapy for women with PPD. They're not just developing drugs; they're trying to shift the entire treatment paradigm.
Official mission statement
Sage Therapeutics' mission is concise and action-oriented. It clearly states the dual goal of innovation and patient benefit, which is the engine driving their pipeline development in neurodevelopmental and neuropsychiatric disorders.
- Pioneer solutions to deliver life-changing brain health medicines, so every person can thrive.
Vision statement
The vision statement sets a high bar for market leadership and global impact. It's a bold declaration of their intent to be the ones who redefine how the world views and treats brain health conditions.
- Fearlessly lead the way to create a world with better brain health.
Given Company slogan/tagline
While not a traditional, single-word slogan, the company's public-facing statement captures their unique scientific approach to the central nervous system (CNS) and their commitment to finding novel solutions where previous treatments have failed. It's about a fresh perspective.
- Seeing the brain differently. makes a world of difference.
Their five core values are the practical framework for how they operate, especially in a high-risk industry where R&D expenses are substantial. Here's the quick math on their commitment: they anticipate overall operating expenses to substantially decrease in 2025 compared to 2024, reflecting a focused, value-driven approach to their pipeline.
- PUT PEOPLE FIRST: Focus on patients, families, and a diverse, equitable, and inclusive internal environment.
- IMPROVE LIVES: Driven by the urgency of those with lived experience of brain health disorders.
- CULTIVATE CURIOSITY: Motivate challenging the status quo and embracing change through active learning.
- DO RIGHT: Operate with integrity, transparency, and accountability to all stakeholders.
- FORGE NEW PATHWAYS: Be courageous, test and learn, and push the boundaries of what is scientifically possible.
Next step: Review the Q3 2025 financial report when available to see if the reduction in operating expenses translates to a smaller net loss.
Sage Therapeutics, Inc. (SAGE) How It Works
Sage Therapeutics, now a wholly-owned subsidiary of Supernus Pharmaceuticals as of July 31, 2025, operates by discovering and developing novel medicines for brain health disorders, primarily leveraging its proprietary neuroactive steroid (NAS) chemistry platform to modulate the GABA-A receptor system-the brain's major inhibitory network. Its business model centers on commercializing its first-in-class oral treatment for postpartum depression (PPD) through a major collaboration, while maintaining a focused, early-stage pipeline in neuropsychiatry.
The company makes money primarily through its 50/50 collaboration with Biogen on ZURZUVAE. For example, in the second quarter of 2025, Sage generated collaboration revenue of $23.2 million from ZURZUVAE sales, reflecting its half of the net revenue Biogen recorded.
Given Company's Product/Service Portfolio
| Product/Service | Target Market | Key Features |
|---|---|---|
| ZURZUVAE (zuranolone) | Adult women with Postpartum Depression (PPD) | First and only FDA-approved oral treatment for PPD; 14-day course of therapy; Neuroactive steroid (NAS) GABA-A receptor positive allosteric modulator (PAM). |
| ZULRESSO (brexanolone) | Adult women with Postpartum Depression (PPD) | First FDA-approved treatment for PPD; IV infusion administered over 60 hours; NAS GABA-A receptor PAM. (Minimal 2025 revenue). |
| SAGE-319 | Behavioral symptoms in certain neurodevelopmental disorders | Phase 1 study data expected late 2025; Extrasynaptic-preferring GABA-A receptor PAM; Designed for a differentiated clinical profile. |
| SAGE-324 | Seizures in Developmental and Epileptic Encephalopathies (DEEs) | Under evaluation for new indications after failing in Essential Tremor; Oral NAS GABA-A receptor PAM; Sage regained full ownership in February 2025. |
Given Company's Operational Framework
You can see the operational shift clearly: Sage has moved from a broad, multi-indication R&D focus to a lean, commercial-first model following the acquisition and pipeline cuts. Honestly, this was a necessary move after the late 2024 trial failures and subsequent restructuring.
The core framework is now built on three pillars:
- Commercial Execution: Jointly commercializing ZURZUVAE with Biogen in the U.S. Biogen handles distribution and logistics, while Sage focuses on market access, sales force expansion, and disease awareness efforts to drive prescription growth, which topped 4,000 shipments in Q2 2025.
- R&D Prioritization: The company significantly reduced its research and development (R&D) expenses, which were down 62.1% in Q2 2025 compared to the prior year, to focus almost exclusively on the most promising early-stage assets like SAGE-319. The entire SAGE-718 program for cognitive impairment was discontinued in late 2024.
- Integration with Supernus: Since the July 2025 acquisition, Sage operates as a subsidiary of Supernus Pharmaceuticals, integrating its commercial operations and CNS expertise into the larger parent company's structure. This is designed to create annual cost synergies of up to $200 million starting in 2026.
Given Company's Strategic Advantages
The company's value proposition is now a blend of a unique, approved product and the financial backing of a larger entity. What this estimate hides is the execution risk in a competitive PPD market.
- First-Mover Advantage in PPD: ZURZUVAE is the only oral, short-course treatment for PPD. This is a defintely critical advantage over the older IV-infusion treatment, ZULRESSO, and traditional antidepressants that take weeks to work.
- Proprietary Neuroactive Steroid Platform: Sage maintains its deep expertise in developing novel neuroactive steroids (NAS) that rapidly modulate GABA-A receptors. This platform allows for the discovery of new treatments for central nervous system (CNS) disorders, which are notoriously difficult to treat.
- Biogen Commercial Collaboration: The 50/50 profit-sharing and co-commercialization agreement with Biogen provides a massive, built-in sales and marketing infrastructure that a smaller biotech could not afford alone, especially for a new-to-market drug.
- Supernus Financial Synergy: The acquisition provides immediate financial stability and a projected cash runway that extends to mid-2027 (as of Q1 2025), plus the expected cost savings from Supernus's existing infrastructure. This shift from a standalone, cash-intensive R&D model to a commercially-focused one under Supernus is the key to near-term survival and growth.
To understand the foundational science and long-term vision that drove this platform, you can read the Mission Statement, Vision, & Core Values of Sage Therapeutics, Inc. (SAGE).
Sage Therapeutics, Inc. (SAGE) How It Makes Money
Sage Therapeutics primarily makes money through revenue sharing from the commercialization of its approved brain health medicines, specifically ZURZUVAE, via a strategic collaboration with Biogen. This collaboration model means revenue is a percentage of the drug's net sales, plus the company earns other revenue from ongoing collaboration activities and milestones.
Sage Therapeutics' Revenue Breakdown
The company's revenue engine in 2025 is overwhelmingly driven by its collaboration with Biogen for ZURZUVAE (zuranolone), the oral treatment for postpartum depression (PPD). The table below reflects the breakdown based on the Q2 2025 results, which showed a total revenue of approximately $31.7 million.
| Revenue Stream | % of Total (Q2 2025) | Growth Trend |
|---|---|---|
| ZURZUVAE Collaboration Revenue | 73% | Increasing |
| Other Collaboration Revenue | 27% | Increasing |
The ZURZUVAE Collaboration Revenue is Sage Therapeutics' 50% share of the net revenue Biogen records from the drug's U.S. sales. The other revenue stream includes payments for development, manufacturing, and other activities under its various collaboration agreements, which saw a sharp jump to $8.5 million in Q2 2025.
Business Economics
The economics of Sage Therapeutics' business are defined by high-value, low-volume pharmaceutical sales and a critical co-commercialization agreement. The focus is on maximizing the adoption of ZURZUVAE, the first-and-only oral treatment for PPD, in a market with a high unmet need.
- Pricing Strategy: The wholesale acquisition cost (WAC) for a full 14-day course of ZURZUVAE is set at $15,900. This price point was established after the drug was not approved for the much larger Major Depressive Disorder (MDD) indication, which had initially factored into pricing discussions.
- Cost-Benefit Rationale: The company justifies this price by citing the high societal cost of PPD, which a 2017 report estimated at $32,300 per woman. They believe the drug offers a clear value proposition to the healthcare system, especially with over 95% of Commercial and Medicaid lives having coverage or a path to coverage as of Q2 2025.
- Collaboration Structure: The partnership with Biogen is a 50/50 net profit-sharing arrangement in the U.S. for ZURZUVAE, meaning Sage Therapeutics shares the commercial risk and reward. This is a smart way to scale a launch without bearing all the massive selling, general, and administrative (SG&A) costs alone.
- Product Transition: The company has defintely shifted its focus, discontinuing its older, infused PPD treatment, ZULRESSO, which generated $0.0 million in revenue in Q1 and Q2 2025 due to its complex 60-hour administration and higher price point of $34,000.
Sage Therapeutics' Financial Performance
While revenue is growing, the company is still in a high-investment, pre-profit stage, a common profile for a biopharmaceutical company focused on a major product launch and pipeline development. The financial story in 2025 is one of accelerating revenue growth coupled with a sharp reduction in operating expenses following a major 2024 restructuring.
- Net Loss Improvement: The net loss for Q2 2025 was $49.7 million, a significant improvement from the $102.9 million loss in the same period of 2024. This shows the cost-saving measures are working.
- Cash Position and Runway: As of June 30, 2025, the company held $366 million in cash, cash equivalents, and marketable securities. This cash position was previously estimated to support operations into mid-2027, but the pending acquisition changes the outlook.
- Expense Management: Research and development (R&D) expenses were tightly controlled, coming in at just $23.7 million in Q2 2025, down from $62.6 million in Q2 2024, reflecting the full impact of the 2024 reorganization and pipeline reprioritization.
- Near-Term Action: The most critical financial event is the pending acquisition by Supernus Pharmaceuticals for up to approximately $795 million, expected to close in Q3 2025. This transaction will fundamentally change the company's financial structure and ownership.
For a deeper dive into the company's long-term vision, you should review the Mission Statement, Vision, & Core Values of Sage Therapeutics, Inc. (SAGE).
Sage Therapeutics, Inc. (SAGE) Market Position & Future Outlook
Sage Therapeutics, Inc. holds a unique, but still nascent, position in the central nervous system (CNS) market, primarily driven by ZURZUVAE (zuranolone), the only FDA-approved oral treatment for postpartum depression (PPD). The company's immediate future is defined by the commercial success of ZURZUVAE, its strategic acquisition by Supernus Pharmaceuticals, and its ability to manage a high cash burn rate while advancing a focused pipeline.
The entire PPD therapeutics market is valued at approximately $1.05 billion in 2025, and ZURZUVAE aims to capture a significant portion of this by disrupting the entrenched use of traditional antidepressants.
Competitive Landscape
The competitive landscape for Sage Therapeutics, Inc. is segmented: it faces entrenched, low-cost generic Selective Serotonin Reuptake Inhibitors (SSRIs) for PPD, but it has a temporary monopoly in the fast-acting, oral neurosteroid class. The PPD market is still heavily dominated by older treatments, but the neuroactive-steroid class is the fastest-growing segment, projected to expand at a 10.25% Compound Annual Growth Rate (CAGR) through 2030.
| Company | Market Share, % (PPD Drug Market) | Key Advantage |
|---|---|---|
| Sage Therapeutics, Inc. (ZURZUVAE) | ~15.7% (Estimated 2025 Net Revenue Proxy) | Only FDA-approved oral, 14-day course for PPD; rapid onset (within 3 days). |
| Generic SSRIs (e.g., Cipla Inc., Pfizer Inc. generics) | 52.23% (2024 PPD Therapeutics Share) | Entrenched first-line status; low cost; long history of use. |
| Brii Biosciences Limited (BRII-296) | <1% (Pipeline) | Developing a single-injection, long-acting therapy for peripartum depression. |
Here's the quick math: ZURZUVAE's collaboration revenue was $23.2 million in Q2 2025, meaning the net revenue recorded by its partner Biogen was $46.4 million for the quarter. That's a strong start for a novel drug, but it's a small fraction of the total $1.05 billion PPD market. Mission Statement, Vision, & Core Values of Sage Therapeutics, Inc. (SAGE).
Opportunities & Challenges
You're looking at a company undergoing a major transition, having been acquired by Supernus Pharmaceuticals, so the future hinges on commercial execution and pipeline data. The core opportunity is establishing ZURZUVAE as the standard of care (SOC) for PPD, a condition affecting an estimated 600,000 women in the U.S. per year.
| Opportunities | Risks |
|---|---|
| Establish ZURZUVAE as PPD Standard of Care. | Commercial execution risk for ZURZUVAE. |
| Supernus Pharmaceuticals acquisition (expected Q3 2025). | High cash burn and net loss. |
| Pipeline Data Readouts in Late 2025. | Reimbursement and market access hurdles. |
- Supernus Pharmaceuticals Acquisition: The acquisition, valued at up to approximately $795 million (including a CVR), is expected to close in Q3 2025, providing immediate capital and commercial infrastructure for ZURZUVAE's growth.
- ZURZUVAE Commercial Momentum: Prescriptions shipped surpassed 13,500 by June 30, 2025, with almost 80% of Q1 2025 prescriptions coming from OB/GYNs, indicating strong initial adoption in the target prescriber base.
- Pipeline Validation: Expect Phase 1 multiple ascending dose (MAD) study data for SAGE-319, a potential treatment for neurodevelopmental disorders, by late 2025.
- Cash Burn: The company is defintely burning through cash, reporting a net loss of $62.2 million in Q1 2025, despite cost-saving measures.
- Reimbursement: ZURZUVAE has a high cost, around $15,900 for the 14-day course in the U.S., which creates a significant barrier to widespread patient access and is a major risk to market growth.
- Generic Competition: SSRIs remain the dominant first-line treatment, holding over 50% of the PPD market share in 2024, challenging ZURZUVAE's premium positioning.
Industry Position
Sage Therapeutics, Inc., post-acquisition by Supernus Pharmaceuticals, is positioned as a niche leader in brain health, specifically in the rapid-acting neurosteroid antidepressant segment. Its core strength is the intellectual property around GABA-A receptor modulation, which is distinct from traditional monoamine-based agents. The company is no longer a pure-play biotech with a massive, high-risk pipeline; it's now a commercial-stage entity focused on scaling its FDA-approved product. The cash position of $366 million as of June 30, 2025, combined with the Supernus backing, provides a runway to mid-2027, allowing for sustained commercial investment in ZURZUVAE. Its industry standing is shifting from a high-risk development firm to a focused commercial asset within a larger, more diversified CNS portfolio.

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