SAGE Therapeutics
SAGE Therapeutics was a clinical-stage biopharmaceutical company developing neurosteroid-based CNS therapeutics, most notably ZURZUVAE (zuranolone), the first FDA-approved oral treatment for postpartum depression. The company was acquired by Supernus Pharmaceuticals in July 2025 for $561-795 million.
- Company typePublic
- Founded2010
- HeadquartersCambridge, United States
- Headcount251–500
- GTM typeB2B
- OfferingHardware or Manufacturing
What SAGE Therapeutics does
SAGE Therapeutics, Inc. was a clinical-stage biopharmaceutical company founded in 2010 and headquartered in Cambridge, Massachusetts, specializing in central nervous system (CNS) therapeutics built on a proprietary neurosteroid platform targeting GABA-A receptors. The company's commercial portfolio centered on postpartum depression (PPD), with ZURZUVAE (zuranolone) — the first FDA-approved oral treatment for PPD, launched in 2023 — and ZULRESSO (brexanolone), an FDA-approved IV infusion for PPD. SAGE's pipeline included SAGE-547 for refractory status epilepticus and exploratory programs in treatment-resistant depression and Tourette syndrome. The business model was a specialty pharmaceutical distribution model: ZURZUVAE was sold through retail and specialty pharmacies via physician prescriptions targeting obstetricians, psychiatrists, and mental health providers, while ZULRESSO was administered in hospital and healthcare facility settings. US commercialization of ZURZUVAE was executed through a partnership with Biogen, which leveraged Biogen's enterprise sales infrastructure to drive over 50,000 prescriptions within 8 months of launch. ZURZUVAE achieved Health Canada authorization in December 2025.
SAGE's revenue mechanics depended on prescription volume, insurance/PBM coverage decisions, and successful physician adoption rather than concentrated anchor contracts, distributing risk across the PPD patient population. The company maintained negative gross profit and EBITDA across disclosed years, reflecting heavy investment in commercial scale-up of ZURZUVAE post-launch and continued R&D spend on the neurosteroid platform. On June 16, 2025, Supernus Pharmaceuticals announced a definitive agreement to acquire SAGE for $561-795 million including upfront cash and contingent value rights tied to ZURZUVAE sales milestones; the transaction closed on July 31, 2025, with Supernus citing approximately $200 million in expected annual cost synergies and diversification into psychiatry as strategic rationale. Following the acquisition, SAGE ceased to operate as an independent public company and now functions as a wholly-owned subsidiary of Supernus, with its neurosteroid platform and PPD franchise integrated into Supernus's broader CNS commercial portfolio.
SAGE Therapeutics firmographics
Firmographics- Name
- SAGE Therapeutics
- Legal name
- Sage Therapeutics, Inc.
- Website
- https://sagerx.com
- Company type
- Public
- Founded year
- 2010
- Operating status
- Acquired
- Headcount range
- 251–500 employees
- Short description
- SAGE Therapeutics was a clinical-stage biopharmaceutical company developing neurosteroid-based CNS therapeutics, most notably ZURZUVAE (zuranolone), the first FDA-approved oral treatment for postpartum depression. The company was acquired by Supernus Pharmaceuticals in July 2025 for $561-795 million.
- Ownership category
- akta.pro rank
SAGE Therapeutics industry classification
Industry- Product category
- CNS Pharmaceuticals
- NAICS
- Biological Product (except Diagnostic) Manufacturing (325414)
- SIC
- Biological Products, (No Disgnostic Substances) (2836)
- akta.pro primary industry
- Neurology & Psychiatry (CNS) Pharmaceuticals (HLAIAAAF)
- akta.pro secondary industries
- Neurology & CNS Specialty Pharmaceuticals (HLAIACAC), Rare Neurology & Neurodegenerative Disorder Therapies (HLAIAIAD)
Keywords
Where SAGE Therapeutics is headquartered
LocationHeadquarters
- HQ city
- Cambridge
- HQ country
- United States
- HQ region
- North America
Offices1 record
Markets served
SAGE Therapeutics business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Technology or R&D, Marketing or Sales, Personnel, Operations, Supply Chain
Revenue model
- ZURZUVAE (zuranolone) sales: FDA-approved oral treatment for postpartum depression generating prescription-based revenue through healthcare providers and pharmacies. Achieved over 50,000 prescriptions within 8 months of launch.
- ZULRESSO (brexanolone) IV infusion: FDA-approved IV treatment for postpartum depression offered as in-office or hospital administration
Go-to-market motion1 record
Distribution channels2 records
Marketing channels3 records
SAGE Therapeutics product offering
Product offeringCore offering
SAGE Therapeutics developed and commercialized novel neurosteroid-based medicines for central nervous system (CNS) disorders. Its commercial portfolio included ZURZUVAE (zuranolone), the first and only FDA-approved oral treatment for postpartum depression, and ZULRESSO (brexanolone), an IV infusion approved for postpartum depression. The company also advanced pipeline therapies targeting refractory status epilepticus, treatment-resistant depression, and Tourette syndrome.
Product overview
SAGE Therapeutics was a biopharmaceutical company focused on central nervous system (CNS) disorders, particularly psychiatric and neurological conditions. Following its acquisition by Supernus Pharmaceuticals in July 2025, its key product ZURZUVAE (zuranolone) became part of Supernus's neuropsychiatry portfolio. ZURZUVAE is the first and only FDA-approved oral treatment for postpartum depression, offering a 14-day treatment regimen with rapid-acting symptom relief.
Differentiator
Problem solved
Functional benefit
Brands
- ZURZUVAE: FDA-approved oral treatment for postpartum depression, the first and only of its kind approved in the United States.
Products and services
- ZURZUVAE (zuranolone) The first FDA-approved oral 14-day treatment for postpartum depression, offering rapid symptom relief starting as early as Day 3 with sustained effects through Day 45. It targets hormonal fluctuations associated with postpartum depression through a neurosteroid mechanism targeting GABA-A receptors.
- ZULRESSO (brexanolone) An FDA-approved IV infusion formulation for the treatment of postpartum depression, administered in hospitals and healthcare facilities as a complementary in-office or hospital administration option.
Quantifiable outcome
- Over 50,000 prescriptions within 8 months of ZURZUVAE launch
- +2 more outcomes
Companies that use SAGE Therapeutics
Customer profileNamed customers1 record
Segments3 records
Ideal customer profiles2 records
SAGE Therapeutics technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature2 records
SAGE Therapeutics partnerships and signals
Strategic signalPartnerships
Three partnerships are on record, tiered core and minor.
- Supernus PharmaceuticalscoreSupernus Pharmaceuticals acquired SAGE Therapeutics for approximately $561-795 million in July 2025. The acquisition included ZURZUVAE and other CNS assets. Supernus diversified its revenue sources and enhanced its psychiatry portfolio with the acquisition, expecting cost synergies of $200 million annually.
- Relmada TherapeuticsminorMichael Quirk, former Chief Scientific Officer and interim Head of R&D at SAGE Therapeutics, was appointed Senior Advisor at Relmada Therapeutics for its sepranolone program, bringing over 20 years of neuroscience drug discovery experience.
- BiogencoreBiogen partnered with SAGE Therapeutics for commercialization of ZURZUVAE (zuranolone) for postpartum depression. Biogen handled commercialization in the US market following FDA approval, with SAGE maintaining certain rights. Biogen also received Health Canada authorization for ZURZUVAE in December 2025.
Scale indicators5 records
Recent moves6 records
Expansion highlights4 records
SAGE Therapeutics competitors and assessment
Company assessmentBroad incumbents
- Acadia Pharmaceuticals: Acadia is a CNS-focused specialty pharmaceutical company (Nuplazid for Parkinson's disease psychosis, Daybue for Rett syndrome). Comparable in targeting niche CNS indications with novel mechanisms and specialty distribution.
- Jazz Pharmaceuticals: Jazz operates a broad CNS/specialty pharma portfolio including psychiatry and neurology assets. Comparable as an established specialty CNS commercializer with overlapping physician call points and payer relationships.
- Intra-Cellular Therapies: Developer of Caplyta (lumateperone) for schizophrenia and bipolar depression. Comparable CNS specialty pharma with psychiatrist-focused commercial model and novel-mechanism psychiatry assets.
Direct peers
- Axsome Therapeutics: Axsome developed Auvelity, an oral rapid-acting antidepressant for major depressive disorder. Directly comparable to Sage in pursuing novel, fast-onset oral CNS therapeutics targeting depression patient populations.
- Marinus Pharmaceuticals: Marinus developed ganaxolone (ZTALMY), a neurosteroid acting on GABA-A receptors — the same mechanistic class as ZURZUVAE/ZULRESSO — for seizure disorders. Most directly comparable peer given the overlapping neurosteroid platform and CNS focus.
Emerging players
- Relmada Therapeutics: Clinical-stage CNS company developing novel depression therapies (including sepranolone, a neurosteroid). Comparable as a smaller CNS developer with overlapping depression pipeline and shared talent with Sage.
- BioXcel Therapeutics: Commercial-stage CNS/biotech company with IGALMI for agitation in schizophrenia/bipolar. Comparable in targeting underserved CNS indications with a small specialty commercial footprint.
- Neumora Therapeutics: Clinical-stage neuroscience company developing precision medicines for brain diseases including depression. Comparable as a well-funded emerging CNS player pursuing novel mechanisms in psychiatry.
- Minerva Neurosciences: Clinical-stage CNS company developing roluperidone for schizophrenia. Comparable as a smaller emerging player with CNS clinical-stage assets targeting psychiatric indications.
- Karuna Therapeutics: Developed Cobenfy (xanomeline-trospium), a novel muscarinic agonist for schizophrenia, acquired by Bristol Myers Squibb. Comparable as an emerging CNS player advancing differentiated mechanisms into psychiatry indications.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat3 records
Key risks6 records
Key highlights7 records
Customer concentration
SAGE Therapeutics social profiles
Digital presenceSAGE Therapeutics financial estimates
Financial estimateRevenue estimate
Valuation estimate
SAGE Therapeutics leadership team
Management profileNumber of profiles
Profiles12 records
SAGE Therapeutics funding detail
Funding detailFunding overview
Funding rounds10 records
Investors6 records
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
SAGE Therapeutics M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about SAGE Therapeutics
What does SAGE Therapeutics do?
SAGE Therapeutics developed and commercialized novel neurosteroid-based medicines for central nervous system (CNS) disorders. Its commercial portfolio included ZURZUVAE (zuranolone), the first and only FDA-approved oral treatment for postpartum depression, and ZULRESSO (brexanolone), an IV infusion approved for postpartum depression. The company also advanced pipeline therapies targeting refractory status epilepticus, treatment-resistant depression, and Tourette syndrome.
Is SAGE Therapeutics a public or private company?
SAGE Therapeutics is a public company. It is classified as public and is currently acquired.
When was SAGE Therapeutics founded?
SAGE Therapeutics was founded in 2010. It employs 251 to 500 people.
Where is SAGE Therapeutics based?
SAGE Therapeutics is headquartered in Cambridge, United States, in the North America region.
How does SAGE Therapeutics make money?
Two revenue lines are on record. ZURZUVAE (zuranolone) sales are the primary driver. The others are ZULRESSO (brexanolone) IV infusion.
Who are SAGE Therapeutics's main competitors?
Broad incumbents on record are Acadia Pharmaceuticals, Jazz Pharmaceuticals and Intra-Cellular Therapies. Direct peers are Axsome Therapeutics and Marinus Pharmaceuticals. Emerging players are Relmada Therapeutics, BioXcel Therapeutics, Neumora Therapeutics, Minerva Neurosciences and Karuna Therapeutics.
Does SAGE Therapeutics have an API?
No public API is recorded for SAGE Therapeutics.
What industry is SAGE Therapeutics in?
SAGE Therapeutics's product category is CNS Pharmaceuticals. Its primary akta.pro industry code is HLAIAAAF, Neurology & Psychiatry (CNS) Pharmaceuticals, with a secondary code of HLAIACAC, Neurology & CNS Specialty Pharmaceuticals. Its NAICS code is 325414 and its SIC code is 2836.