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Syremis Therapeutics

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uuid00c23nq

Namestring
Syremis Therapeutics
Legal namestring
Syremis Therapeutics Ltd.
Websiteurl
syremis.com
Company typeenum
Private
Founded yearint
2025
Descriptiontext

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.

Short descriptiontext

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.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersTel Aviv, Israel
HQ citystring
Tel Aviv
HQ countrystring
Israel
HQ regionstring
Middle East
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
neuropsychiatric drug development, muscarinic receptor agonists, NMDA receptor antagonists, schizophrenia therapeutics, depression drug pipeline
Industry1 code
1DTx/SaMD Regulatory, Quality & Compliance Software (QMS/ISO/FDA)
CodeHLACANANPrimaryYes
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Neuropsychiatric Pharmaceuticals
Social media profiles1 record
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Cost components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Others
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

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.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

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.

Product and service2 records
1ST-905
CategoryDrug Candidate
Description

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.

2ST-901
CategoryDrug Candidate
Description

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.

Scale indicator3 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierCoreTypeTechnology or Integration
Description

Syremis's pipeline programs ST-905 and ST-901 originated from Clexio Biosciences, indicating an intellectual property or technology licensing relationship.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

CNS-focused specialty biopharma with Lybalvi (schizophrenia, bipolar) and other neuropsychiatric assets. Operates directly in Syremis's lead indications with commercial-stage infrastructure.

TypeBroad incumbent
Description

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.

TypeBroad incumbent
Description

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.

TypeBroad incumbent
Description

Markets aripiprazole franchise (Abilify, Abilify Asimtufii, Rexulti) covering schizophrenia and adjunctive depression. Established incumbent in the exact indications Syremis targets.

TypeBroad incumbent
Description

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.

TypeDirect peer
Description

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.

TypeBroad incumbent
Description

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.

TypeDirect peer
Description

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.

TypeEmerging player
Description

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.

TypeDirect peer
Description

Clinical-stage neuropsychiatry company developing navacaprant (M4 antagonist) for schizophrenia alongside other CNS programs. Pursues precision psychiatry in the same symptom domains Syremis targets.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat2 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment2 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature2 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles14 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds1 record

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors6 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Syremis Therapeutics

Neuropsychiatric Pharmaceuticalssyremis.com

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.

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

  • Neuropsychiatric drug development
  • Muscarinic receptor agonists
  • NMDA receptor antagonists
  • Schizophrenia therapeutics
  • Depression drug pipeline

Where Syremis Therapeutics is headquartered

Location

Headquarters

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 offering

Core 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 profile

Segments2 records

Ideal customer profiles3 records

Syremis Therapeutics technology and API

Technology

Technology 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 signal

Partnerships

One partnership is on record.

  • Clexio BiosciencescoreTechnology or IntegrationSyremis'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 assessment

Broad 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 presence

Syremis Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Syremis Therapeutics leadership team

Management profile

Number of profiles

Profiles14 records

Syremis Therapeutics funding detail

Funding detail

Funding 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 investment

M&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.

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Live signals
Labiotech.euRace for approval: biotechs accelerate bipolar disorder therapiesAutobahn Therapeutics reported positive Phase 2 results for its oral drug elunetirom in treating bipolar depression, with 75% of 21 patients responding to treatment and a statistically significant 16.8-point improvement on the HAMD-17 depression scale after six weeks. Patients also recovered significant work productivity, reducing lost workdays from 2.7 to 0.4 days per week. The company received FDA Fast Track Designation for elunetirom, while Syremis Therapeutics, Rapport Therapeutics, and Alto Neuroscience are advancing additional novel mechanisms targeting bipolar disorder, with multiple pivotal readouts expected in 2026.GlobesIsrael missing out on global life sciences recoveryIsrael's life sciences sector stagnated in 2025, with investment falling to $1.4 billion from $2 billion in 2024. The report, from IATI and the Israel Innovation Authority, shows a decline in medical devices and public market offerings, though the 89bio sale to Roche for $2.4 billion offsets some losses.VentureBeatSyremis Therapeutics Appoints Dr. Aaron Koenig as Chief Medical OfficerSyremis Therapeutics appointed Dr. Aaron Koenig as Chief Medical Officer, bringing neuropsychiatric drug development experience. He previously led CMO roles at Syndeio Biosciences and Delix Therapeutics. The appointment aims to support the company's pipeline, including its lead program ST-905 in Phase 1.ynetnewsIsrael’s 'traumatech' sector surges as mental health funding jumps 150%Israel’s mental health technology sector experienced a 150% surge in funding in 2025, reaching $352 million across 178 companies, according to the Mental Health Innovation Map 2026 released at HealthIL Week, with four large deals (Syremis Therapeutics $165M, Empathy $72M, Eleos $60M, Sensi.AI $45M) driving the majority of investment despite a drop in total deal count from 20 to 13 rounds. The sector is maturing from early-stage consumer apps toward evidence-based therapeutics, AI-powered managed care, and later-stage funding rounds, with experts noting Israel as a growing "living lab" for mental health innovation and 80% of the ecosystem still in startup or early development phase.The Media LineIsrael’s ‘Traumatech’ Boom Draws Investment as Mental Health Innovation MaturesIsrael's mental health technology sector, known as 'traumatech,' has attracted $352 million in funding over the past year, representing a 150% increase according to the Mental Health Innovation Map released at HealthIL Week, with 178 companies now operating in the space. Investment is shifting toward technologies demonstrating clinical results within health systems rather than consumer wellness applications, with companies like Syremis Therapeutics, Empathy, Eleos, and Sensi.AI securing significant rounds. Regulatory alignment is accelerating as the US FDA begins clearing prescription digital therapeutics and Israel's Health Ministry explores integrating these tools into the public health system.CTechIsraeli startups raise over $1.6 billion in December, marking strongest funding monthIsraeli startups raised $1.635 billion across 22 funding rounds in December, marking the strongest month for venture funding in the country since 2022. Data security company Cyera led with a $400 million round at a $9 billion valuation, while Eon secured $300 million and other firms like Vega and Syremis also attracted significant investment. Cybersecurity and artificial intelligence sectors dominated the landscape, reflecting sustained investor interest in these high-growth areas.Pulse 2.0Syremis Therapeutics Launches With $165 Million Series A Funding To Advance New Schizophrenia And Depression Drug ProgramsSyremis Therapeutics has launched as a clinical-stage biopharmaceutical company focused on mental health with $165 million in Series A financing to advance a neuropsychiatric pipeline. The funding round was co-led by Dexcel Pharma and Third Rock Ventures, with participation from Bain Capital Life Sciences, GV, QVT, and Pictet, to support clinical development of lead program ST-905 for schizophrenia and ST-901 for major depressive disorder and bipolar depression. Both drug candidates were initially discovered and developed at Clexio Biosciences before being spun out into Syremis, with Phase 1 trials for ST-905 already underway.CTechSyremis raises $165 million Series A to take on schizophrenia and other severe mentalSyremis Therapeutics, a clinical-stage biopharmaceutical company focused on severe mental illness, has raised $165 million in Series A financing to develop treatments for conditions such as schizophrenia. The company plans to advance its lead programs, including ST-905 for schizophrenia and neuropsychiatric conditions, and ST-901 for depression, through clinical trials.BioSpaceSyremis Therapeutics Launches with $165M to Develop Best-in-Class Medicines for Mental Health ConditionsSyremis Therapeutics has launched with a $165 million Series A financing to develop novel medicines for mental health conditions. The funding, co-led by Dexcel Pharma and Third Rock Ventures, will support the advancement of its lead program ST-905 through clinical proof of concept.FinSMEsSyremis Therapeutics Raises $165M in Series A FinancingSyremis Therapeutics raised $165M in Series A financing co-led by Dexcel Pharma and Third Rock Ventures. The funds will advance its neuropsychiatric pipeline, including Phase 1 dual M1/M4 agonist ST-905 and NMDA antagonist ST-901. The company plans to use the capital for clinical proof of concept.