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Noema Pharma

Full company profile

uuid0000j8m

Namestring
Noema Pharma
Legal namestring
Noema Pharma AG
Company typeenum
Private
Founded yearint
2019
Descriptiontext

Noema Pharma is a Swiss-based, clinical-stage biotechnology company founded in 2019 and headquartered in Basel, developing a portfolio of oral small molecule therapeutics for central nervous system (CNS) disorders. The company's pipeline consists of four drug candidates in-licensed from Roche: basimglurant (NOE-101), a first-in-class mGluR5 negative allosteric modulator in Phase 2/3 for trigeminal neuralgia (FDA Fast Track designated) and seizures in tuberous sclerosis complex; gemlapodect (NOE-105), a first-in-class PDE10A inhibitor in Phase 2b for Tourette syndrome and childhood onset fluency disorder (stuttering); cendifensine (NOE-115), a broad-spectrum monoamine modulator in Phase 2a for menopausal vasomotor symptoms, where Phase 2a results showed a 92.3% reduction in daily hot flash frequency; and NOE-109, an mGluR2/3 inhibitor in preclinical validation. Basimglurant has established safety data in over 1,000 subjects and gemlapodect Phase 2a data showed no metabolic side effects compared to current antipsychotic standards of care.

The company targets patient populations across both orphan and large-market neurology indications, including approximately 140,000 US trigeminal neuralgia patients, 80,000 US/EU TSC patients, over 500,000 US Tourette syndrome patients, and roughly 27 million US menopausal women. Noema has raised over CHF 287 million (~$325M) across a Series A (2020), Series B (2023), and Series B extension (2024) from a syndicate including Sofinnova Partners, Polaris Partners, Forbion, Jeito Capital, Gilde Healthcare, Invus, UPMC Enterprises, and EQT Life Sciences. Leadership includes CEO Ilise Lombardo, MD (formerly Kriya Therapeutics, Arvelle Therapeutics), Chairman Jeffrey Jonas (former CEO of Sage Therapeutics), EVP R&D Volker Knappertz, MD (led Epidiolex approval at GW Pharmaceuticals), and CMO Rob Lasser, MD (led zuranolone at Sage Therapeutics), reflecting deep CNS drug development expertise.

Noema operates a pre-revenue, sales-led biotech model focused on advancing its pipeline through clinical trials toward regulatory approval and eventual commercialization via prescription pharmaceutical channels, either directly or through partnership with larger pharmaceutical companies. The company employs a multi-stakeholder engagement strategy including patient advocacy partnerships (Facial Pain Association, TSC Alliance, World Stuttering Network), KOL webinars, and investor conference participation, while maintaining offices in Basel, Switzerland and the Boston Area, United States to support global clinical trial operations across the US, Europe, and Australia.

Short descriptiontext

Noema Pharma is a Swiss clinical-stage biotech developing four oral small molecule CNS drug candidates in-licensed from Roche, targeting trigeminal neuralgia, tuberous sclerosis complex seizures, Tourette syndrome, stuttering, and menopausal vasomotor symptoms, with four active Phase 2 trials and over CHF 287 million raised.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersBasel, Switzerland
HQ citystring
Basel
HQ countrystring
Switzerland
HQ regionstring
Europe
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
CNS drug development, oral small molecules, neurology therapeutics, trigeminal neuralgia treatment, menopausal vasomotor therapy
Industry4 codes
1Neurology & CNS Specialty Pharmaceuticals
CodeHLAIACACPrimaryYes
2Neurology & Psychiatry (CNS) Pharmaceuticals
CodeHLAIAAAFPrimaryNo
3Rare Neurology & Neurodegenerative Disorder Therapies
CodeHLAIAIADPrimaryNo
4Endocrinology & Reproductive Health Pharmaceuticals (incl. Women’s Health)
CodeHLAIAAAJPrimaryNo
NAICS code1 code
  • Pharmaceutical Preparation Manufacturing325412
Product category
CNS Therapeutics / Neurology Pharmaceuticals
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Pharmaceutical drug development and commercialization
TypeOne Time License
Description

Pre-revenue clinical-stage biotech. The company develops proprietary therapeutic candidates through clinical trials, seeks regulatory approval (FDA, EMA), and commercializes drugs via prescription pathway, either directly or through partnership with a larger pharmaceutical company. Revenue would be generated from product sales upon regulatory approval.

noemapharma.com
Marketing channels8 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, 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

Noema Pharma develops oral small molecule therapeutics targeting central nervous system disorders, with a portfolio of four clinical-stage drug candidates in-licensed from Roche. The lead assets address trigeminal neuralgia pain, seizures in tuberous sclerosis complex, Tourette syndrome, stuttering, and menopausal vasomotor symptoms through well-characterized mechanisms including mGluR5 inhibition, PDE10A inhibition, and broad-spectrum monoamine modulation.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 6 values shown
  • Cendifensine (30 mg dose): 92.3% reduction in daily frequency of moderate-to-severe hot flashes from baseline to Week 12, with mean reduction of 12.3 daily hot flashes (LS mean adjusted p<0.001)
+5 more records
Product overview1 text field

Noema Pharma is advancing a late-stage portfolio of oral small molecule therapeutics targeting neurological and related disorders. The company is developing four clinical-stage drug candidates in-licensed from Roche: Basimglurant (NOE-101), a Phase 2/3 mGluR5 NAM for trigeminal neuralgia and seizures in TSC; Cendifensine (NOE-115), a Phase 2a broad-spectrum monoamine modulator for menopausal vasomotor symptoms; Gemlapodect (NOE-105), a Phase 2b PDE10A inhibitor for Tourette syndrome and stuttering; and NOE-109, an mGluR2/3 inhibitor in preclinical validation.

Product and service4 records
1Basimglurant (NOE-101)
CategoryDrug Candidate - mGluR5 NAM
Description

Potential first-in-class, highly selective and potent mGluR5 negative allosteric modulator (NAM) being developed for the management of pain associated with trigeminal neuralgia (TN) and seizure control in tuberous sclerosis complex (TSC). Oral, once-daily dosing; tested in over 1,000 subjects with favorable tolerability and no known abuse potential. Currently in Phase 2/3 clinical trials with FDA Fast Track designation.

2Gemlapodect (NOE-105)
CategoryDrug Candidate - PDE10A Inhibitor
Description

First-in-class oral PDE10A inhibitor that modulates dopamine signaling exclusively in medium spiny neurons of the striatum. Being developed for Tourette syndrome and Childhood Onset Fluency Disorder (stuttering). Phase 2a ALLEVIA-1 study met primary and all key secondary endpoints; now in Phase 2b trials. No metabolic side effects (weight gain, insulin resistance) observed in clinical studies.

3Cendifensine (NOE-115)
CategoryDrug Candidate - Monoamine Modulator
Description

Oral broad-spectrum monoamine modulator designed as a non-hormonal treatment for vasomotor symptoms (VMS/hot flashes & night sweats) and other menopause-related symptoms. Rebalances serotonin, norepinephrine, and dopamine. Phase 2a results demonstrated 92.3% reduction in daily hot flash frequency and 59.2% reduction in VMS severity at 12 weeks, with median weight reduction of 2.5 kg.

4NOE-109
Scale indicator10 records

Each record includes

Type, Value, Description, Source

Partnership5 partners
Strategic tierCoreTypeOEM/ Whitelabel/ Licensing Partner
Description

Licensed four mid-clinical-stage therapeutic product candidates from Roche: NOE-101 (mGluR5 inhibitor), NOE-105 (PDE10A inhibitor), NOE-109 (mGluR2/3 inhibitor), and NOE-115 (triple reuptake inhibitor/monoamine modulator). All assets have established safety data from prior clinical testing.

Strategic tierSupportingTypeStrategic or Co-development Partner
Description

Patient advocacy organization for trigeminal neuralgia. Logo displayed on Noema Pharma's website. The Facial Pain Association provides resources and support for TN patients, a key patient population for Noema's lead asset basimglurant.

3World Stuttering Network
Strategic tierSupportingTypeStrategic or Co-development Partner
Description

Patient advocacy organization for people who stutter. Logo displayed on Noema Pharma's website. The World Stuttering Network supports patients with childhood onset fluency disorder (stuttering), a target indication for gemlapodect (NOE-105).

noemapharma.com
Strategic tierSupportingTypeStrategic or Co-development Partner
Description

Published podcast on its website dedicated to basimglurant (NOE-101) and seizures associated with tuberous sclerosis complex. Patient advocacy partner for TSC, a key indication for NOE-101.

Strategic tierSupportingTypeStrategic or Co-development Partner
Description

Operates Noema Pharma's website as a processor within the meaning of the EU GDPR. Provides investor relations, media, and communications services to Noema Pharma.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Specialty CNS pharmaceutical company commercializing Nuplazid (pimavanserin) for Parkinson's disease psychosis and other CNS therapies. Comparable as a broader CNS specialty pharma focused on neurology/psychiatry with approved and pipeline assets.

TypeDirect peer
Description

CNS-focused biotech that developed and launched Auvelity for major depressive disorder. Comparable as a small-cap clinical-stage CNS company with multiple late-stage CNS assets and a similar specialty commercialization model.

TypeBroad incumbent
Description

Global pharma that launched Veozah (fezolinetant) for menopausal vasomotor symptoms, directly competing with Noema's cendifensine program. Comparable as a large-pharma competitor with an approved non-hormonal menopause therapy in the same indication Noema is pursuing.

TypeDirect peer
Description

Clinical-stage CNS biotech that developed xanomeline/trospium (Cobenfy) for schizophrenia before being acquired by Bristol Myers Squibb. Directly comparable as a CNS-focused clinical-stage biotech that advanced a single novel-mechanism therapy to FDA approval via Phase 3.

TypeDirect peer
Description

Clinical-stage CNS biotech that developed and commercialized zuranolone (ZURZUVAE) for postpartum depression and has worked extensively in neurology and psychiatry. Noema's CMO Robert Lasser led zuranolone development at Sage, and Chairman Jeffrey Jonas is Sage's former CEO, making it a direct comparable in CNS small-molecule development.

TypeDirect peer
Description

CNS and neurology-focused biotech that developed Nurtec ODT for migraine before divesting that asset to Pfizer. Comparable as a multi-asset CNS clinical-stage company that ultimately exited via a large-pharma transaction.

TypeBroad incumbent
Description

Specialty CNS pharma that acquired GW Pharmaceuticals and commercialized Epidiolex (cannabidiol) for rare epilepsies, including TSC. Volker Knappertz (Noema EVP R&D) led Epidiolex's development at GW. Highly comparable as an established CNS player in rare epilepsies.

TypeEmerging player
Description

CNS-focused company that developed Caplyta (lumateperone) for schizophrenia and bipolar depression before being acquired by Johnson & Johnson. Comparable as a CNS small-molecule company that progressed from clinical stage to commercial launch and strategic exit.

TypeDirect peer
Description

Clinical-stage CNS company that developed Ztalmy (ganaxolone) for CDKL5 deficiency disorder, an orphan epilepsy. Comparable as a small CNS biotech pursuing rare neurology with FDA-approved orphan CNS drug.

TypeDirect peer
Description

Clinical-stage biotech developing CNS therapies including epilepsy (PRAX-222 for SCN1A-related disorders) and other rare neurology indications. Comparable as a small CNS-focused clinical-stage biotech pursuing orphan neurology indications.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment5 records

Each record includes

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

Ideal customer profile5 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
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles19 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 rounds3 records

Each record includes

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

Investors9 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 →

Noema Pharma

CNS Therapeutics / Neurology Pharmaceuticalsnoemapharma.com

Noema Pharma is a Swiss clinical-stage biotech developing four oral small molecule CNS drug candidates in-licensed from Roche, targeting trigeminal neuralgia, tuberous sclerosis complex seizures, Tourette syndrome, stuttering, and menopausal vasomotor symptoms, with four active Phase 2 trials and over CHF 287 million raised.

What Noema Pharma does

Noema Pharma is a Swiss-based, clinical-stage biotechnology company founded in 2019 and headquartered in Basel, developing a portfolio of oral small molecule therapeutics for central nervous system (CNS) disorders. The company's pipeline consists of four drug candidates in-licensed from Roche: basimglurant (NOE-101), a first-in-class mGluR5 negative allosteric modulator in Phase 2/3 for trigeminal neuralgia (FDA Fast Track designated) and seizures in tuberous sclerosis complex; gemlapodect (NOE-105), a first-in-class PDE10A inhibitor in Phase 2b for Tourette syndrome and childhood onset fluency disorder (stuttering); cendifensine (NOE-115), a broad-spectrum monoamine modulator in Phase 2a for menopausal vasomotor symptoms, where Phase 2a results showed a 92.3% reduction in daily hot flash frequency; and NOE-109, an mGluR2/3 inhibitor in preclinical validation. Basimglurant has established safety data in over 1,000 subjects and gemlapodect Phase 2a data showed no metabolic side effects compared to current antipsychotic standards of care.

The company targets patient populations across both orphan and large-market neurology indications, including approximately 140,000 US trigeminal neuralgia patients, 80,000 US/EU TSC patients, over 500,000 US Tourette syndrome patients, and roughly 27 million US menopausal women. Noema has raised over CHF 287 million (~$325M) across a Series A (2020), Series B (2023), and Series B extension (2024) from a syndicate including Sofinnova Partners, Polaris Partners, Forbion, Jeito Capital, Gilde Healthcare, Invus, UPMC Enterprises, and EQT Life Sciences. Leadership includes CEO Ilise Lombardo, MD (formerly Kriya Therapeutics, Arvelle Therapeutics), Chairman Jeffrey Jonas (former CEO of Sage Therapeutics), EVP R&D Volker Knappertz, MD (led Epidiolex approval at GW Pharmaceuticals), and CMO Rob Lasser, MD (led zuranolone at Sage Therapeutics), reflecting deep CNS drug development expertise.

Noema operates a pre-revenue, sales-led biotech model focused on advancing its pipeline through clinical trials toward regulatory approval and eventual commercialization via prescription pharmaceutical channels, either directly or through partnership with larger pharmaceutical companies. The company employs a multi-stakeholder engagement strategy including patient advocacy partnerships (Facial Pain Association, TSC Alliance, World Stuttering Network), KOL webinars, and investor conference participation, while maintaining offices in Basel, Switzerland and the Boston Area, United States to support global clinical trial operations across the US, Europe, and Australia.

Noema Pharma firmographics

Firmographics
Name
Noema Pharma
Legal name
Noema Pharma AG
Website
https://noemapharma.com/
Company type
Private
Founded year
2019
Operating status
Operating
Headcount range
11–50 employees
Short description
Noema Pharma is a Swiss clinical-stage biotech developing four oral small molecule CNS drug candidates in-licensed from Roche, targeting trigeminal neuralgia, tuberous sclerosis complex seizures, Tourette syndrome, stuttering, and menopausal vasomotor symptoms, with four active Phase 2 trials and over CHF 287 million raised.
Ownership category
akta.pro rank

Noema Pharma industry classification

Industry
Product category
CNS Therapeutics / Neurology Pharmaceuticals
NAICS
Pharmaceutical Preparation Manufacturing (325412)
akta.pro primary industry
Neurology & CNS Specialty Pharmaceuticals (HLAIACAC)
akta.pro secondary industries
Neurology & Psychiatry (CNS) Pharmaceuticals (HLAIAAAF), Rare Neurology & Neurodegenerative Disorder Therapies (HLAIAIAD), Endocrinology & Reproductive Health Pharmaceuticals (incl. Women’s Health) (HLAIAAAJ)

Keywords

  • CNS drug development
  • Oral small molecules
  • Neurology therapeutics
  • Trigeminal neuralgia treatment
  • Menopausal vasomotor therapy

Where Noema Pharma is headquartered

Location

Headquarters

HQ city
Basel
HQ country
Switzerland
HQ region
Europe

Offices2 records

Markets served

Noema Pharma business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Operations, Marketing or Sales, Others

Revenue model

  1. Pharmaceutical drug development and commercialization: Pre-revenue clinical-stage biotech. The company develops proprietary therapeutic candidates through clinical trials, seeks regulatory approval (FDA, EMA), and commercializes drugs via prescription pathway, either directly or through partnership with a larger pharmaceutical company. Revenue would be generated from product sales upon regulatory approval.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels8 records

Noema Pharma product offering

Product offering

Core offering

Noema Pharma develops oral small molecule therapeutics targeting central nervous system disorders, with a portfolio of four clinical-stage drug candidates in-licensed from Roche. The lead assets address trigeminal neuralgia pain, seizures in tuberous sclerosis complex, Tourette syndrome, stuttering, and menopausal vasomotor symptoms through well-characterized mechanisms including mGluR5 inhibition, PDE10A inhibition, and broad-spectrum monoamine modulation.

Product overview

Noema Pharma is advancing a late-stage portfolio of oral small molecule therapeutics targeting neurological and related disorders. The company is developing four clinical-stage drug candidates in-licensed from Roche: Basimglurant (NOE-101), a Phase 2/3 mGluR5 NAM for trigeminal neuralgia and seizures in TSC; Cendifensine (NOE-115), a Phase 2a broad-spectrum monoamine modulator for menopausal vasomotor symptoms; Gemlapodect (NOE-105), a Phase 2b PDE10A inhibitor for Tourette syndrome and stuttering; and NOE-109, an mGluR2/3 inhibitor in preclinical validation.

Differentiator

Problem solved

Functional benefit

Products and services

  • Basimglurant (NOE-101) Potential first-in-class, highly selective and potent mGluR5 negative allosteric modulator (NAM) being developed for the management of pain associated with trigeminal neuralgia (TN) and seizure control in tuberous sclerosis complex (TSC). Oral, once-daily dosing; tested in over 1,000 subjects with favorable tolerability and no known abuse potential. Currently in Phase 2/3 clinical trials with FDA Fast Track designation.
  • Gemlapodect (NOE-105) First-in-class oral PDE10A inhibitor that modulates dopamine signaling exclusively in medium spiny neurons of the striatum. Being developed for Tourette syndrome and Childhood Onset Fluency Disorder (stuttering). Phase 2a ALLEVIA-1 study met primary and all key secondary endpoints; now in Phase 2b trials. No metabolic side effects (weight gain, insulin resistance) observed in clinical studies.
  • Cendifensine (NOE-115) Oral broad-spectrum monoamine modulator designed as a non-hormonal treatment for vasomotor symptoms (VMS/hot flashes & night sweats) and other menopause-related symptoms. Rebalances serotonin, norepinephrine, and dopamine. Phase 2a results demonstrated 92.3% reduction in daily hot flash frequency and 59.2% reduction in VMS severity at 12 weeks, with median weight reduction of 2.5 kg.
  • NOE-109

Quantifiable outcome

  • Cendifensine (30 mg dose): 92.3% reduction in daily frequency of moderate-to-severe hot flashes from baseline to Week 12, with mean reduction of 12.3 daily hot flashes (LS mean adjusted p<0.001)
  • +5 more outcomes

Companies that use Noema Pharma

Customer profile

Segments5 records

Ideal customer profiles5 records

Noema Pharma technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Noema Pharma partnerships and signals

Strategic signal

Partnerships

Five partnerships are on record, tiered core and supporting.

  • RochecoreOEM/ Whitelabel/ Licensing PartnerLicensed four mid-clinical-stage therapeutic product candidates from Roche: NOE-101 (mGluR5 inhibitor), NOE-105 (PDE10A inhibitor), NOE-109 (mGluR2/3 inhibitor), and NOE-115 (triple reuptake inhibitor/monoamine modulator). All assets have established safety data from prior clinical testing.
  • Facial Pain AssociationsupportingStrategic or Co-development PartnerPatient advocacy organization for trigeminal neuralgia. Logo displayed on Noema Pharma's website. The Facial Pain Association provides resources and support for TN patients, a key patient population for Noema's lead asset basimglurant.
  • World Stuttering NetworksupportingStrategic or Co-development PartnerPatient advocacy organization for people who stutter. Logo displayed on Noema Pharma's website. The World Stuttering Network supports patients with childhood onset fluency disorder (stuttering), a target indication for gemlapodect (NOE-105).
  • TSC AlliancesupportingStrategic or Co-development PartnerPublished podcast on its website dedicated to basimglurant (NOE-101) and seizures associated with tuberous sclerosis complex. Patient advocacy partner for TSC, a key indication for NOE-101.
  • LifeSci CommunicationssupportingStrategic or Co-development PartnerOperates Noema Pharma's website as a processor within the meaning of the EU GDPR. Provides investor relations, media, and communications services to Noema Pharma.

Scale indicators10 records

Recent moves6 records

Expansion highlights6 records

Noema Pharma competitors and assessment

Company assessment

Broad incumbents

  • Acadia Pharmaceuticals: Specialty CNS pharmaceutical company commercializing Nuplazid (pimavanserin) for Parkinson's disease psychosis and other CNS therapies. Comparable as a broader CNS specialty pharma focused on neurology/psychiatry with approved and pipeline assets.
  • Astellas Pharma: Global pharma that launched Veozah (fezolinetant) for menopausal vasomotor symptoms, directly competing with Noema's cendifensine program. Comparable as a large-pharma competitor with an approved non-hormonal menopause therapy in the same indication Noema is pursuing.
  • Jazz Pharmaceuticals: Specialty CNS pharma that acquired GW Pharmaceuticals and commercialized Epidiolex (cannabidiol) for rare epilepsies, including TSC. Volker Knappertz (Noema EVP R&D) led Epidiolex's development at GW. Highly comparable as an established CNS player in rare epilepsies.

Direct peers

  • Axsome Therapeutics: CNS-focused biotech that developed and launched Auvelity for major depressive disorder. Comparable as a small-cap clinical-stage CNS company with multiple late-stage CNS assets and a similar specialty commercialization model.
  • Karuna Therapeutics: Clinical-stage CNS biotech that developed xanomeline/trospium (Cobenfy) for schizophrenia before being acquired by Bristol Myers Squibb. Directly comparable as a CNS-focused clinical-stage biotech that advanced a single novel-mechanism therapy to FDA approval via Phase 3.
  • Sage Therapeutics: Clinical-stage CNS biotech that developed and commercialized zuranolone (ZURZUVAE) for postpartum depression and has worked extensively in neurology and psychiatry. Noema's CMO Robert Lasser led zuranolone development at Sage, and Chairman Jeffrey Jonas is Sage's former CEO, making it a direct comparable in CNS small-molecule development.
  • Biohaven Pharmaceuticals: CNS and neurology-focused biotech that developed Nurtec ODT for migraine before divesting that asset to Pfizer. Comparable as a multi-asset CNS clinical-stage company that ultimately exited via a large-pharma transaction.
  • Marinus Pharmaceuticals: Clinical-stage CNS company that developed Ztalmy (ganaxolone) for CDKL5 deficiency disorder, an orphan epilepsy. Comparable as a small CNS biotech pursuing rare neurology with FDA-approved orphan CNS drug.
  • Praxis Precision Medicines: Clinical-stage biotech developing CNS therapies including epilepsy (PRAX-222 for SCN1A-related disorders) and other rare neurology indications. Comparable as a small CNS-focused clinical-stage biotech pursuing orphan neurology indications.

Emerging players

  • Intra-Cellular Therapies: CNS-focused company that developed Caplyta (lumateperone) for schizophrenia and bipolar depression before being acquired by Johnson & Johnson. Comparable as a CNS small-molecule company that progressed from clinical stage to commercial launch and strategic exit.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

Noema Pharma social profiles

Digital presence

Noema Pharma financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Noema Pharma leadership team

Management profile

Number of profiles

Profiles19 records

Noema Pharma funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors9 records

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

Noema Pharma 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 Noema Pharma

What does Noema Pharma do?

Noema Pharma develops oral small molecule therapeutics targeting central nervous system disorders, with a portfolio of four clinical-stage drug candidates in-licensed from Roche. The lead assets address trigeminal neuralgia pain, seizures in tuberous sclerosis complex, Tourette syndrome, stuttering, and menopausal vasomotor symptoms through well-characterized mechanisms including mGluR5 inhibition, PDE10A inhibition, and broad-spectrum monoamine modulation.

Is Noema Pharma a public or private company?

Noema Pharma is a private company. It is classified as venture growth investor backed and is currently operating.

When was Noema Pharma founded?

Noema Pharma was founded in 2019. It employs 11 to 50 people.

Where is Noema Pharma based?

Noema Pharma is headquartered in Basel, Switzerland, in the Europe region.

How does Noema Pharma make money?

One revenue line is on record: pharmaceutical drug development and commercialization.

Who are Noema Pharma's main competitors?

Broad incumbents on record are Acadia Pharmaceuticals, Astellas Pharma and Jazz Pharmaceuticals. Direct peers are Axsome Therapeutics, Karuna Therapeutics, Sage Therapeutics, Biohaven Pharmaceuticals, Marinus Pharmaceuticals and Praxis Precision Medicines. Intra-Cellular Therapies is listed as an emerging player.

Does Noema Pharma have an API?

No public API is recorded for Noema Pharma.

What industry is Noema Pharma in?

Noema Pharma's product category is CNS Therapeutics / Neurology Pharmaceuticals. Its primary akta.pro industry code is HLAIACAC, Neurology & CNS Specialty Pharmaceuticals, with a secondary code of HLAIAAAF, Neurology & Psychiatry (CNS) Pharmaceuticals. Its NAICS code is 325412.

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PR NewswireVasomotor Symptoms Market Poised for Growth Through 2036, Driven by Rising Adoption of Hormonal and Non-Hormonal Therapies | DelveInsightThe vasomotor symptoms market is expected to grow through 2036, driven by rising adoption of hormonal and non-hormonal therapies. The US held the largest market share in 2025, with prevalence reaching 60-80% in postmenopausal women. Emerging drugs like cendifensine and asimadoline are advancing in clinical trials.Markets DailyNoema Pharma plc (NASDAQ:NOEMW) Short Interest UpdateNoema Pharma's short interest fell 72.2% to 1,705 shares as of August 14, down from 6,139 shares on July 30, with a short-interest ratio of 0.2 days on an average volume of 6,999 shares. The stock rose $0.01 to $0.15 on Friday, trading at 553 shares, below its 50-day moving average of $0.14.GlobeNewswireNoema Pharma to Present Phase 2a Results for Cendifensine in Vasomotor Symptoms (Hot Flashes) Due to Menopause at the 2026 ACOG Annual Clinical & Scientific MeetingNoema Pharma will present Phase 2a results for cendifensine at the 2026 ACOG meeting, showing 92% reduction in VMS frequency and 59% in severity over 12 weeks. The data also show improvements in mood, cravings, and fatigue, with median weight loss of 2.5 kg, supporting a Phase 2b trial.GlobeNewswireNoema Pharma Announces Phase 2a Study Results with Cendifensine in Women with Vasomotor Symptoms (Hot Flashes) Due to MenopauseNoema Pharma announced positive Phase 2a results for cendifensine in menopausal women with hot flashes. The 12-week study showed a 92.3% mean reduction in daily hot flashes and 59.2% reduction in severity at 30 mg, with similar benefits at 60 mg. The company plans to advance to a Phase 2b study next year.BioSpaceNoema Pharma Announces Phase 2a Study Results with Cendifensine in Women with Vasomotor Symptoms (Hot Flashes) Due to MenopauseNoema Pharma AG announced positive topline results from a Phase 2a open-label study of cendifensine in 35 menopausal women experiencing moderate-to-severe vasomotor symptoms. The 30mg dose achieved a mean 92.3% reduction in daily hot flash frequency and 59.2% reduction in severity at 12 weeks, with the treatment generally well tolerated and no serious adverse events reported. The company plans to advance cendifensine into a Phase 2b study next year as a potential non-hormonal therapeutic option targeting temperature dysregulation and other menopausal symptoms.GlobeNewswireNoema Pharma Appoints Volker Knappertz, M.D., as Executive Vice President of Research & DevelopmentNoema Pharma appointed Volker Knappertz, M.D., as Executive Vice President of Research & Development. He previously led R&D at Aurinia Pharmaceuticals and GW Pharmaceuticals, where he helped obtain FDA approval for Epidiolex. Noema's Phase 2 studies are expected to have readouts in 2025.Pulse 2.0Noema Pharma: Biotech Company Closes Series B At About $147 MillionNoema Pharma closed a Series B extension financing round with EQT Life Sciences, bringing total capital raised to CHF 130 million (about $147 million). The funding supports four active Phase 2 trials, with key data readouts anticipated in 2025. The round follows a CHF 103 million Series B and a CHF 54 million Series A.Gilde HealthcareGilde Healthcare Portfolio Company Noema Pharma extends Series B financing round - Gilde HealthcareNoema Pharma announced the successful close of a Series B extension financing round, raising an additional investment from EQT Life Sciences to bring the total capital raised to CHF 130 million. The new funding will support four active Phase 2 clinical trials for central nervous system disorders, with key data readouts anticipated in 2025. This extension follows initial Series B and Series A rounds, strengthening the investor syndicate that includes Gilde Healthcare and others.European BiotechnologyNoema Pharma AG extends Series B financingNoema Pharma AG has closed a CHF27m Series B extension financing round led by EQT Life Sciences, bringing the total capital raised in this series to CHF130m. The new funds will support the development of four active Phase II programmes licensed from Roche, with key data readouts expected in 2025.The Pharma LetterHuge backing for Noema’s neuroscience goalNoema Pharma, a Swiss biotech company, announced the successful closing of a Series B extension financing round. The investment was provided by EQT Life Sciences to support the company's goals in treating central nervous system disorders.