Syremis Therapeutics
Syremis Therapeutics is a clinical-stage biopharmaceutical company developing ST-905 (M1/M4 muscarinic agonist in Phase 1) and ST-901 (NMDA antagonist in IND-enabling studies) for schizophrenia, major depressive disorder, and bipolar depression, headquartered in Tel Aviv with a Boston operations hub.
- Company typePrivate
- Founded2025
- HeadquartersTel Aviv, Israel
- Headcount11–50
- GTM typeB2B
- OfferingHardware or Manufacturing
What Syremis Therapeutics does
Syremis Therapeutics Ltd. is a clinical-stage biopharmaceutical company founded in December 2025 and headquartered in Tel Aviv, Israel with a secondary operations hub in Boston, Massachusetts. The company is developing a neuropsychiatric drug pipeline targeting major unmet needs in mental health, with two lead programs: ST-905, a dual M1/M4 preferential muscarinic agonist currently in Phase 1 development for schizophrenia and related serious psychiatric conditions; and ST-901, a next-generation NMDA receptor antagonist in IND-enabling studies for major depressive disorder and bipolar depression. Both candidates were in-licensed from Clexio Biosciences, and the company is led by co-founder and CEO Elisabeth Kogan alongside co-founder Steve Paul (former CEO and Chair of Karuna Therapeutics), with a board that includes representatives from Bain Capital Life Sciences, Third Rock Ventures, and Dexcel Pharma.
Syremis targets three large and underserved CNS indications: schizophrenia (affecting more than 20 million people worldwide), major depressive disorder, and bipolar depression. The scientific thesis is that muscarinic M1/M4 agonism can address both positive symptoms (via M4-mediated reduction of mesostriatal dopamine) and negative and cognitive symptoms (via M1 receptors in the prefrontal cortex) of schizophrenia, while next-generation NMDA antagonism could deliver a more rapid antidepressant effect than the 4–6 week onset of current standard-of-care medications. The company was launched with a $165 million Series A funding round led by Bain Capital Life Sciences, with participation from Third Rock Ventures, Dexcel Pharma, Google Ventures, Pictet, and QVT Financial.
The business model is standard clinical-stage biopharma: Syremis is pre-revenue, does not currently have commercialized products, and is not yet subject to product pricing or distribution. The capital raised in the Series A is being deployed to advance ST-905 through Phase 1 and ST-901 into IND submission, with the goal of reaching clinical proof of concept before any partnering, out-licensing, or commercialization decision. Long-term value creation is expected through either an IPO, strategic acquisition, or partnership transaction with a larger pharmaceutical company that can fund pivotal trials and commercial launch. Customer segments, in the eventual commercial sense, will be patients with schizophrenia, MDD, and bipolar depression, reached through traditional pharma sales, payer reimbursement, and physician channels following regulatory approval.
Syremis Therapeutics firmographics
Firmographics- Name
- Syremis Therapeutics
- Legal name
- Syremis Therapeutics Ltd.
- Website
- https://syremis.com
- Company type
- Private
- Founded year
- 2025
- Operating status
- Operating
- Headcount range
- 11–50 employees
- Short description
- Syremis Therapeutics is a clinical-stage biopharmaceutical company developing ST-905 (M1/M4 muscarinic agonist in Phase 1) and ST-901 (NMDA antagonist in IND-enabling studies) for schizophrenia, major depressive disorder, and bipolar depression, headquartered in Tel Aviv with a Boston operations hub.
- Ownership category
- akta.pro rank
Syremis Therapeutics industry classification
Industry- Product category
- Neuropsychiatric Pharmaceuticals
- SIC
- Pharmaceutical Preparations (2834)
- akta.pro primary industry
- DTx/SaMD Regulatory, Quality & Compliance Software (QMS/ISO/FDA) (HLACANAN)
Keywords
Where Syremis Therapeutics is headquartered
LocationHeadquarters
- HQ city
- Tel Aviv
- HQ country
- Israel
- HQ region
- Middle East
Offices2 records
Markets served
Syremis Therapeutics business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Technology or R&D, Personnel, Operations, Marketing or Sales, Others
Marketing channels4 records
Syremis Therapeutics product offering
Product offeringCore offering
Syremis Therapeutics is a clinical-stage biopharmaceutical company developing two small-molecule drug candidates for serious mental health conditions. Its lead asset, ST-905, is a dual M1/M4 muscarinic agonist in Phase 1 development for schizophrenia and other serious neuropsychiatric conditions. Its second asset, ST-901, is a next-generation NMDA receptor antagonist in IND-enabling studies for major depressive disorder and bipolar depression, designed to provide a more rapid antidepressant effect than existing medications.
Product overview
Syremis Therapeutics is a clinical-stage biopharmaceutical company developing a neuropsychiatric drug pipeline rooted in emerging and clinically validated mechanisms. The company operates two lead programs: ST-905, a dual M1/M4 muscarinic agonist in Phase 1 for schizophrenia, and ST-901, a next-generation NMDA antagonist in IND-enabling studies for major depressive disorder and bipolar depression. Both drug candidates target different neurotransmitter pathways to address significant unmet needs in mental health treatment.
Differentiator
Problem solved
Functional benefit
Products and services
- ST-905 ST-905 is a potent M1/M4 preferential muscarinic agonist currently in Phase 1 clinical development for the treatment of schizophrenia and other serious neuropsychiatric conditions. It targets M1 and M4 receptors in brain regions linked to schizophrenia symptoms and modulates neurotransmitters including acetylcholine, dopamine, GABA, and glutamate to address positive, negative, and cognitive symptoms.
- ST-901 ST-901 is a novel NMDA receptor antagonist in IND-enabling studies, being developed for major depressive disorder and bipolar depression. It is designed to provide a more rapid antidepressant effect than most current medications, which typically take 4-6 weeks.
Companies that use Syremis Therapeutics
Customer profileSegments2 records
Ideal customer profiles3 records
Syremis Therapeutics technology and API
TechnologyTechnology focussed No
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature2 records
Syremis Therapeutics partnerships and signals
Strategic signalPartnerships
One partnership is on record.
- Clexio BiosciencescoreSyremis's pipeline programs ST-905 and ST-901 originated from Clexio Biosciences, indicating an intellectual property or technology licensing relationship.
Scale indicators3 records
Recent moves6 records
Expansion highlights4 records
Syremis Therapeutics competitors and assessment
Company assessmentBroad incumbents
- Alkermes: CNS-focused specialty biopharma with Lybalvi (schizophrenia, bipolar) and other neuropsychiatric assets. Operates directly in Syremis's lead indications with commercial-stage infrastructure.
- Intra-Cellular Therapies: Developed Caplyta (lumateperone), an approved therapy for schizophrenia and bipolar depression, and was acquired by J&J for ~$14.6B. Competes in both of Syremis's target indications.
- Acadia Pharmaceuticals: Established CNS specialty company with Nuplazid approved for Parkinson's disease psychosis; pursuing additional neuropsychiatric indications. Serves the same psychiatrist prescriber base that would prescribe ST-905/ST-901.
- Otsuka Pharmaceutical: Markets aripiprazole franchise (Abilify, Abilify Asimtufii, Rexulti) covering schizophrenia and adjunctive depression. Established incumbent in the exact indications Syremis targets.
- Sage Therapeutics: CNS-focused biopharma (now part of Biogen) that brought Zurzuvae to market for postpartum depression and has broader neuropsychiatric pipeline. Overlaps Syremis in CNS drug development capability and depression indication.
- Axsome Therapeutics: Commercial-stage CNS specialty company with Auvelity (NMDA-targeting combination) approved for major depressive disorder. Direct competitor to Syremis's ST-901 fast-onset depression program.
Direct peers
- Cerevel Therapeutics: Developed emraclidine, an M4-selective agonist for schizophrenia, before being acquired by AbbVie for ~$8.7B. Closest direct competitor to ST-905 in the muscarinic agonist space; Ray Sanchez (Syremis board) was Cerevel's former CMO.
- Karuna Therapeutics: Karuna pioneered M1/M4 muscarinic agonism in schizophrenia with xanomeline/trospium (now Cobenfy, acquired by Bristol-Myers Squibb for ~$14B). Directly comparable mechanism of action and indication focus to ST-905.
- Neumora Therapeutics: Clinical-stage neuropsychiatry company developing navacaprant (M4 antagonist) for schizophrenia alongside other CNS programs. Pursues precision psychiatry in the same symptom domains Syremis targets.
Emerging players
- MapLight Therapeutics: Clinical-stage CNS company focused on schizophrenia and other neuropsychiatric disorders using novel pharmacology including muscarinic and NMDA mechanisms. Smaller, earlier-stage competitor with overlapping pipeline.
Market position
Strengths4 records
Weaknesses5 records
Competitive moat2 records
Key risks5 records
Key highlights6 records
Customer concentration
Syremis Therapeutics social profiles
Digital presenceSyremis Therapeutics financial estimates
Financial estimateRevenue estimate
Valuation estimate
Syremis Therapeutics leadership team
Management profileNumber of profiles
Profiles14 records
Syremis Therapeutics funding detail
Funding detailFunding overview
Funding rounds1 record
Investors6 records
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Syremis 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 Syremis Therapeutics
What does Syremis Therapeutics do?
Syremis Therapeutics is a clinical-stage biopharmaceutical company developing two small-molecule drug candidates for serious mental health conditions. Its lead asset, ST-905, is a dual M1/M4 muscarinic agonist in Phase 1 development for schizophrenia and other serious neuropsychiatric conditions. Its second asset, ST-901, is a next-generation NMDA receptor antagonist in IND-enabling studies for major depressive disorder and bipolar depression, designed to provide a more rapid antidepressant effect than existing medications.
Is Syremis Therapeutics a public or private company?
Syremis Therapeutics is a private company. It is classified as venture growth investor backed and is currently operating.
When was Syremis Therapeutics founded?
Syremis Therapeutics was founded in 2025. It employs 11 to 50 people.
Where is Syremis Therapeutics based?
Syremis Therapeutics is headquartered in Tel Aviv, Israel, in the Middle East region.
Who are Syremis Therapeutics's main competitors?
Broad incumbents on record are Alkermes, Intra-Cellular Therapies, Acadia Pharmaceuticals, Otsuka Pharmaceutical, Sage Therapeutics and Axsome Therapeutics. Direct peers are Cerevel Therapeutics, Karuna Therapeutics and Neumora Therapeutics. MapLight Therapeutics is listed as an emerging player.
Does Syremis Therapeutics have an API?
No public API is recorded for Syremis Therapeutics.
What industry is Syremis Therapeutics in?
Syremis Therapeutics's product category is Neuropsychiatric Pharmaceuticals. Its primary akta.pro industry code is HLACANAN, DTx/SaMD Regulatory, Quality & Compliance Software (QMS/ISO/FDA). Its SIC code is 2834.