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HAYA Therapeutics

Full company profile

uuid000044u

Namestring
HAYA Therapeutics
Legal namestring
HAYA Therapeutics SA
Websiteurl
hayatx.com
Company typeenum
Private
Founded yearint
2019
Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersLausanne, Switzerland
HQ citystring
Lausanne
HQ countrystring
Switzerland
HQ regionstring
Europe
Markets served

Serves global market

Offices3 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
RNA-guided therapeutics, antisense oligonucleotide therapy, non-coding RNA discovery, cardiac fibrosis treatment, regulatory genome platform
Industry2 codes
1Antisense Oligonucleotides (ASO) Therapeutics (splice modulation/knockdown)
CodeHLAAADACPrimaryYes
2RNA Therapeutics Platforms & Design (sequence design, target ID/validation, AI/bioinformatics)
CodeHLAAADAGPrimaryNo
NAICS code1 code
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
RNA-targeted Therapeutics
Social media profiles2 records
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model3 records
1Biopharma Partnerships & Licensing (Lilly collaboration)
TypeLicensing Royalties
Description

Multi-year collaboration with Eli Lilly (announced Sept 2024) for discovery of RNA-based drug targets in obesity and metabolic disorders. HAYA receives an upfront payment (including equity investment) and is eligible for up to an aggregate $1 billion in pre-clinical, clinical and commercial milestone payments, plus royalties on product sales. Revenue is milestone-driven and not recurring.

hayatx.com
2Venture Capital Financing (Pre-Revenue)
TypeProfessional Services
Description

HAYA is a clinical-stage biotechnology company that is pre-revenue. Capital is raised through equity financing rounds (CHF 18M seed in 2021, US$5M seed extension in 2022 bringing total seed to ~US$25M, US$65M Series A in 2025) led by Sofinnova Partners, Earlybird Venture Capital, Eli Lilly, and other investors. No product sales or commercial revenue yet.

hayatx.com
3Future Product Sales (HTX-001, pipeline)
TypeOne Time License
Description

Lead candidate HTX-001 is an antisense oligonucleotide currently in Phase 1 clinical trials (first cohort dosed May 2026) for nonobstructive hypertrophic cardiomyopathy (nHCM); future revenue would come from commercialization of RNA-guided therapeutics in cardiac, pulmonary, and oncology indications, plus future out-licensing deals.

hayatx.com
Marketing channels7 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Personnel, Technology or R&D, Operations, Infrastructure, Marketing or Sales
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 of 2 records shown
1HAYAtlas
Description

Proprietary unified, scalable engine (HAYAtlas™) that links non-coding RNAs to complex disease causality and predicts their potential to reprogram cell fate, powering HAYA's target nomination.

hayatx.com
+1 more record
Core offering1 text field

HAYA Therapeutics develops precision RNA-guided medicines (antisense oligonucleotides) that target long non-coding RNAs in the 'dark genome' to reprogram disease-driving cell states. Its lead candidate HTX-001 is an anti-WISPER ASO in Phase 1 clinical trials for nonobstructive hypertrophic cardiomyopathy (nHCM), with additional pipeline programs in pulmonary fibrosis, oncology, and metabolic diseases. The company operates a partnership-driven business model, exemplified by its multi-year Eli Lilly collaboration for obesity and metabolic disease drug targets.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 6 values shown
  • 30–80% new lncRNAs identified per cell-state vs GENCODE
+5 more records
Product overview1 text field

HAYA Therapeutics offers a platform-plus-programs architecture centered on its proprietary HAYAtlas (Regulatory Genome Engine) — a causally-informative atlas combining multimodal functional genomics with computational and machine learning methodologies to decode the 98% of the genome that does not code for proteins. Built on this core platform, HAYA develops a portfolio of first-in-class RNA-guided antisense oligonucleotide (ASO) therapeutics, with its lead candidate HTX-001 (Wisper) in Phase 1 clinical development for nonobstructive hypertrophic cardiomyopathy (nHCM). The same platform powers additional pipeline programs spanning pulmonary (idiopathic pulmonary fibrosis & rejuvenation), oncology (solid tumors), and new discovery programs in other common and chronic diseases, all accelerated through strategic collaborations.

Product and service5 records
1HTX-001 (anti-WISPER ASO)
CategoryLead Therapeutic Candidate
Description

HAYA's lead investigational candidate — a first-in-class antisense oligonucleotide designed to downregulate WISPER lncRNA, a heart stress-specific long non-coding RNA overexpressed in patients with hypertrophic cardiomyopathy. The therapeutic targets WISPER in cardiac myofibroblast cells to promote cell-state reprogramming of the fibrotic/pathological cell population back to a healthy state. Currently in Phase 1a/b clinical trial for nonobstructive hypertrophic cardiomyopathy (nHCM).

2Pulmonary Program (Idiopathic Pulmonary Fibrosis & Rejuvenation)
CategoryPipeline Program
Description

HAYA's pulmonary pipeline program targeting idiopathic pulmonary fibrosis (IPF) and lung rejuvenation. Developed using the HAYAtlas platform to identify lncRNA targets in pulmonary fibrosis and lung cell states. Target identity currently undisclosed.

3Oncology Program (Solid Tumors)
CategoryPipeline Program
Description

HAYA's oncology pipeline program targeting solid tumors using lncRNA-targeting precision RNA therapies. Modality is currently agnostic. Leverages the HAYAtlas platform for target identification in tumor-related cell states.

4New Discovery Programs
CategoryPipeline Program
Description

HAYA's broader new discovery programs targeting other common and chronic diseases, accelerated through strategic collaborations. Builds on the versatility of the HAYAtlas platform to address additional fibrotic, metabolic, and age-related disease indications.

5RNA-Guided Discovery Collaboration (Eli Lilly multi-year program for obesity and metabolic disease)
CategoryStrategic Collaboration / Out-Licensing Program
Description

A co-development and out-licensing offering in which HAYA applies its proprietary RNA-guided regulatory genome platform to identify and validate multiple RNA-based drug targets in obesity and metabolic disease for Eli Lilly. HAYA receives upfront and equity, plus up to $1 billion in potential milestones and royalties — one of the largest collaborations to date in the regulatory genome space.

Scale indicator12 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-06-03
Description

HAYA relocated its US site to Lilly Gateway Labs in San Diego (operated in partnership with Alexandria Real Estate Equities) on June 3, 2025. The site provides cutting-edge laboratory space, operational support, and access to an evolving ecosystem of biotech innovators, supporting HAYA's multi-modal functional genomics work and clinical development of HTX-001. HAYA remains fully independent and retains all assets and intellectual property.

Strategic tierFlagshipTypeStrategic or Co-development PartnerAnnounced on2024-09-04
Description

Multi-year collaboration (announced Sept 4, 2024) for HAYA to apply its proprietary RNA-guided regulatory genome platform to support preclinical drug discovery in obesity and related metabolic conditions. Partners will identify multiple regulatory-genome-derived RNA-based drug targets. HAYA receives an upfront payment (including equity investment) and is eligible for up to an aggregate $1 billion in pre-clinical, clinical and commercial milestone payments, plus royalties on product sales. Described as one of the largest collaborations to date in the regulatory genome space. Eli Lilly also participated in HAYA's $65M Series A (May 2025) and hosts HAYA's San Diego operations at Lilly Gateway Labs.

Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2022-02-09
Description

HAYA established a new laboratory space at JLABS @ San Diego (part of Johnson & Johnson Innovation's global network of life science incubators) in February 2022, enabling expansion of its US operations alongside the CHF 18M seed round and $5M seed extension. HAYA later relocated to Lilly Gateway Labs in June 2025.

Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2021-05-21
Description

HAYA secured an exclusive license from CHUV (Centre Hospitalier Universitaire Vaudois / Lausanne University Hospital) for the Wisper asset, the cardiac-tissue-enriched lncRNA discovered by co-founder Samir Ounzain during his academic research at CHUV. This license is the foundational IP enabling HAYA's lead program HTX-001 (anti-WISPER antisense oligonucleotide) for cardiac fibrosis.

Recent move8 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Clinical-stage biotech developing genetic and cardiovascular medicines, including programs targeting hypertrophic cardiomyopathy (e.g., acoramidis for ATTR-CM). Comparable as a cardiovascular-focused biotech with multiple programs and a pipeline model analogous to HAYA's.

TypeDirect peer
Description

Cardiovascular genetic medicine company developing in vivo gene editing therapies for heart disease. Barry Ticho (HAYA independent director) co-founded Verve, and both companies pursue disease-modifying approaches to cardiac conditions using nucleic-acid-based modalities.

TypeEmerging player
Description

RNA-targeting small molecule developer with a platform-plus-pipeline model focused on splicing and RNA biology. Comparable to HAYA as a platform company leveraging proprietary RNA-biology science to generate a portfolio of therapeutics across multiple indications.

TypeBroad incumbent
Description

The leading RNA-targeted therapeutics company, using RNAi rather than ASOs but operating in the same broad RNA-medicine category with a platform-pipeline model and major pharma partnerships analogous to HAYA's Lilly deal.

TypeDirect peer
Description

RNA-targeted antisense oligonucleotide company developing precision medicines for genetic diseases, with similar platform-plus-pipeline architecture to HAYA. Notably, Barry Ticho (HAYA independent director) is CMO at Stoke, indicating direct personnel overlap in the ASO/RNA therapeutic space.

TypeDirect peer
Description

Clinical-stage genetic medicines company focused on heart disease, including hypertrophic cardiomyopathy. Directly comparable to HAYA's cardiac fibrosis/nHCM focus, with competing modalities (gene therapy, small molecules) targeting similar patient populations.

TypeOthers
Description

AI-driven drug discovery platform using computational biology and high-throughput experimentation. HAYA's CBO Richard Law helped lead the Recursion/Exscientia merger, and Recursion's platform-plus-pharma-partnership model parallels HAYA's strategy of leveraging proprietary biology/AI tools to secure large-pharma collaborations.

TypeDirect peer
Description

Cardiology-focused genetic medicine company developing RNA- and gene-therapy-based treatments for cardiovascular diseases. HAYA's CMO Jordan Shin was previously SVP at LEXEO, and both companies target overlapping cardiac indications including cardiomyopathies.

TypeDirect peer
Description

Clinical-stage RNA-targeted therapeutics company developing antisense oligonucleotides for serious muscle diseases. Directly comparable modality (ASOs) and platform architecture to HAYA, though focused on muscle rather than cardiac/fibrotic indications.

TypeBroad incumbent
Description

The foundational antisense oligonucleotide (ASO) company and pioneer of the modality HAYA uses. HAYA's VP Translation (James Karras) previously worked at Ionis, and Ionis serves as the benchmark for ASO-based therapeutic platforms across multiple disease areas.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 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

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
Yes
API detail
Has APIbool
No

Docs URL, Description

AI capability5 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature6 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles15 records

Each record includes

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

Subsidiaries1 record

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

Compliance2 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds12 records

Each record includes

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

Investors19 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 →

HAYA Therapeutics

RNA-targeted Therapeuticshayatx.com

HAYA Therapeutics firmographics

Firmographics
Name
HAYA Therapeutics
Legal name
HAYA Therapeutics SA
Website
https://hayatx.com
Company type
Private
Founded year
2019
Operating status
Operating
Headcount range
11–50 employees
Ownership category
akta.pro rank

HAYA Therapeutics industry classification

Industry
Product category
RNA-targeted Therapeutics
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Antisense Oligonucleotides (ASO) Therapeutics (splice modulation/knockdown) (HLAAADAC)
akta.pro secondary industry
RNA Therapeutics Platforms & Design (sequence design, target ID/validation, AI/bioinformatics) (HLAAADAG)

Keywords

  • RNA-guided therapeutics
  • Antisense oligonucleotide therapy
  • Non-coding RNA discovery
  • Cardiac fibrosis treatment
  • Regulatory genome platform

Where HAYA Therapeutics is headquartered

Location

Headquarters

HQ city
Lausanne
HQ country
Switzerland
HQ region
Europe

Offices3 records

Markets served

HAYA Therapeutics business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Technology or R&D, Operations, Infrastructure, Marketing or Sales

Revenue model

  1. Biopharma Partnerships & Licensing (Lilly collaboration): Multi-year collaboration with Eli Lilly (announced Sept 2024) for discovery of RNA-based drug targets in obesity and metabolic disorders. HAYA receives an upfront payment (including equity investment) and is eligible for up to an aggregate $1 billion in pre-clinical, clinical and commercial milestone payments, plus royalties on product sales. Revenue is milestone-driven and not recurring.
  2. Venture Capital Financing (Pre-Revenue): HAYA is a clinical-stage biotechnology company that is pre-revenue. Capital is raised through equity financing rounds (CHF 18M seed in 2021, US$5M seed extension in 2022 bringing total seed to ~US$25M, US$65M Series A in 2025) led by Sofinnova Partners, Earlybird Venture Capital, Eli Lilly, and other investors. No product sales or commercial revenue yet.
  3. Future Product Sales (HTX-001, pipeline): Lead candidate HTX-001 is an antisense oligonucleotide currently in Phase 1 clinical trials (first cohort dosed May 2026) for nonobstructive hypertrophic cardiomyopathy (nHCM); future revenue would come from commercialization of RNA-guided therapeutics in cardiac, pulmonary, and oncology indications, plus future out-licensing deals.

Go-to-market motion3 records

Distribution channels3 records

Marketing channels7 records

HAYA Therapeutics product offering

Product offering

Core offering

HAYA Therapeutics develops precision RNA-guided medicines (antisense oligonucleotides) that target long non-coding RNAs in the 'dark genome' to reprogram disease-driving cell states. Its lead candidate HTX-001 is an anti-WISPER ASO in Phase 1 clinical trials for nonobstructive hypertrophic cardiomyopathy (nHCM), with additional pipeline programs in pulmonary fibrosis, oncology, and metabolic diseases. The company operates a partnership-driven business model, exemplified by its multi-year Eli Lilly collaboration for obesity and metabolic disease drug targets.

Product overview

HAYA Therapeutics offers a platform-plus-programs architecture centered on its proprietary HAYAtlas (Regulatory Genome Engine) — a causally-informative atlas combining multimodal functional genomics with computational and machine learning methodologies to decode the 98% of the genome that does not code for proteins. Built on this core platform, HAYA develops a portfolio of first-in-class RNA-guided antisense oligonucleotide (ASO) therapeutics, with its lead candidate HTX-001 (Wisper) in Phase 1 clinical development for nonobstructive hypertrophic cardiomyopathy (nHCM). The same platform powers additional pipeline programs spanning pulmonary (idiopathic pulmonary fibrosis & rejuvenation), oncology (solid tumors), and new discovery programs in other common and chronic diseases, all accelerated through strategic collaborations.

Differentiator

Problem solved

Functional benefit

Brands

  • HAYAtlas: Proprietary unified, scalable engine (HAYAtlas™) that links non-coding RNAs to complex disease causality and predicts their potential to reprogram cell fate, powering HAYA's target nomination.
  • DiscoverHAYA

Products and services

  • HTX-001 (anti-WISPER ASO) HAYA's lead investigational candidate — a first-in-class antisense oligonucleotide designed to downregulate WISPER lncRNA, a heart stress-specific long non-coding RNA overexpressed in patients with hypertrophic cardiomyopathy. The therapeutic targets WISPER in cardiac myofibroblast cells to promote cell-state reprogramming of the fibrotic/pathological cell population back to a healthy state. Currently in Phase 1a/b clinical trial for nonobstructive hypertrophic cardiomyopathy (nHCM).
  • Pulmonary Program (Idiopathic Pulmonary Fibrosis & Rejuvenation) HAYA's pulmonary pipeline program targeting idiopathic pulmonary fibrosis (IPF) and lung rejuvenation. Developed using the HAYAtlas platform to identify lncRNA targets in pulmonary fibrosis and lung cell states. Target identity currently undisclosed.
  • Oncology Program (Solid Tumors) HAYA's oncology pipeline program targeting solid tumors using lncRNA-targeting precision RNA therapies. Modality is currently agnostic. Leverages the HAYAtlas platform for target identification in tumor-related cell states.
  • New Discovery Programs HAYA's broader new discovery programs targeting other common and chronic diseases, accelerated through strategic collaborations. Builds on the versatility of the HAYAtlas platform to address additional fibrotic, metabolic, and age-related disease indications.
  • RNA-Guided Discovery Collaboration (Eli Lilly multi-year program for obesity and metabolic disease) A co-development and out-licensing offering in which HAYA applies its proprietary RNA-guided regulatory genome platform to identify and validate multiple RNA-based drug targets in obesity and metabolic disease for Eli Lilly. HAYA receives upfront and equity, plus up to $1 billion in potential milestones and royalties — one of the largest collaborations to date in the regulatory genome space.

Quantifiable outcome

  • 30–80% new lncRNAs identified per cell-state vs GENCODE
  • +5 more outcomes

Companies that use HAYA Therapeutics

Customer profile

Ideal customer profiles3 records

HAYA Therapeutics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability5 records

Feature6 records

HAYA Therapeutics partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered core, flagship and minor.

  • Lilly Gateway Labs (Lilly Catalyze360 / Alexandria Real Estate Equities)coreStrategic or Co-development Partner · 3 June 2025HAYA relocated its US site to Lilly Gateway Labs in San Diego (operated in partnership with Alexandria Real Estate Equities) on June 3, 2025. The site provides cutting-edge laboratory space, operational support, and access to an evolving ecosystem of biotech innovators, supporting HAYA's multi-modal functional genomics work and clinical development of HTX-001. HAYA remains fully independent and retains all assets and intellectual property.
  • Eli Lilly and CompanyflagshipStrategic or Co-development Partner · 4 September 2024Multi-year collaboration (announced Sept 4, 2024) for HAYA to apply its proprietary RNA-guided regulatory genome platform to support preclinical drug discovery in obesity and related metabolic conditions. Partners will identify multiple regulatory-genome-derived RNA-based drug targets. HAYA receives an upfront payment (including equity investment) and is eligible for up to an aggregate $1 billion in pre-clinical, clinical and commercial milestone payments, plus royalties on product sales. Described as one of the largest collaborations to date in the regulatory genome space. Eli Lilly also participated in HAYA's $65M Series A (May 2025) and hosts HAYA's San Diego operations at Lilly Gateway Labs.
  • JLABS @ San Diego (Johnson & Johnson Innovation)minorStrategic or Co-development Partner · 9 February 2022HAYA established a new laboratory space at JLABS @ San Diego (part of Johnson & Johnson Innovation's global network of life science incubators) in February 2022, enabling expansion of its US operations alongside the CHF 18M seed round and $5M seed extension. HAYA later relocated to Lilly Gateway Labs in June 2025.
  • CHUV (Lausanne University Hospital)coreOEM/ Whitelabel/ Licensing Partner · 21 May 2021HAYA secured an exclusive license from CHUV (Centre Hospitalier Universitaire Vaudois / Lausanne University Hospital) for the Wisper asset, the cardiac-tissue-enriched lncRNA discovered by co-founder Samir Ounzain during his academic research at CHUV. This license is the foundational IP enabling HAYA's lead program HTX-001 (anti-WISPER antisense oligonucleotide) for cardiac fibrosis.

Scale indicators12 records

Recent moves8 records

Expansion highlights6 records

HAYA Therapeutics competitors and assessment

Company assessment

Broad incumbents

  • BridgeBio Pharma: Clinical-stage biotech developing genetic and cardiovascular medicines, including programs targeting hypertrophic cardiomyopathy (e.g., acoramidis for ATTR-CM). Comparable as a cardiovascular-focused biotech with multiple programs and a pipeline model analogous to HAYA's.
  • Alnylam Pharmaceuticals: The leading RNA-targeted therapeutics company, using RNAi rather than ASOs but operating in the same broad RNA-medicine category with a platform-pipeline model and major pharma partnerships analogous to HAYA's Lilly deal.
  • Ionis Pharmaceuticals: The foundational antisense oligonucleotide (ASO) company and pioneer of the modality HAYA uses. HAYA's VP Translation (James Karras) previously worked at Ionis, and Ionis serves as the benchmark for ASO-based therapeutic platforms across multiple disease areas.

Direct peers

  • Verve Therapeutics: Cardiovascular genetic medicine company developing in vivo gene editing therapies for heart disease. Barry Ticho (HAYA independent director) co-founded Verve, and both companies pursue disease-modifying approaches to cardiac conditions using nucleic-acid-based modalities.
  • Stoke Therapeutics: RNA-targeted antisense oligonucleotide company developing precision medicines for genetic diseases, with similar platform-plus-pipeline architecture to HAYA. Notably, Barry Ticho (HAYA independent director) is CMO at Stoke, indicating direct personnel overlap in the ASO/RNA therapeutic space.
  • Tenaya Therapeutics: Clinical-stage genetic medicines company focused on heart disease, including hypertrophic cardiomyopathy. Directly comparable to HAYA's cardiac fibrosis/nHCM focus, with competing modalities (gene therapy, small molecules) targeting similar patient populations.
  • LEXEO Therapeutics: Cardiology-focused genetic medicine company developing RNA- and gene-therapy-based treatments for cardiovascular diseases. HAYA's CMO Jordan Shin was previously SVP at LEXEO, and both companies target overlapping cardiac indications including cardiomyopathies.
  • Dyne Therapeutics: Clinical-stage RNA-targeted therapeutics company developing antisense oligonucleotides for serious muscle diseases. Directly comparable modality (ASOs) and platform architecture to HAYA, though focused on muscle rather than cardiac/fibrotic indications.

Emerging players

  • Skyhawk Therapeutics: RNA-targeting small molecule developer with a platform-plus-pipeline model focused on splicing and RNA biology. Comparable to HAYA as a platform company leveraging proprietary RNA-biology science to generate a portfolio of therapeutics across multiple indications.

Others

  • Recursion Pharmaceuticals: AI-driven drug discovery platform using computational biology and high-throughput experimentation. HAYA's CBO Richard Law helped lead the Recursion/Exscientia merger, and Recursion's platform-plus-pharma-partnership model parallels HAYA's strategy of leveraging proprietary biology/AI tools to secure large-pharma collaborations.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

HAYA Therapeutics social profiles

Digital presence

HAYA Therapeutics compliance and trust

Trust signal

Compliance2 records

HAYA Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

HAYA Therapeutics leadership team

Management profile

Number of profiles

Profiles15 records

HAYA Therapeutics subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

HAYA Therapeutics funding detail

Funding detail

Funding overview

Funding rounds12 records

Investors19 records

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

HAYA 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 HAYA Therapeutics

What does HAYA Therapeutics do?

HAYA Therapeutics develops precision RNA-guided medicines (antisense oligonucleotides) that target long non-coding RNAs in the 'dark genome' to reprogram disease-driving cell states. Its lead candidate HTX-001 is an anti-WISPER ASO in Phase 1 clinical trials for nonobstructive hypertrophic cardiomyopathy (nHCM), with additional pipeline programs in pulmonary fibrosis, oncology, and metabolic diseases. The company operates a partnership-driven business model, exemplified by its multi-year Eli Lilly collaboration for obesity and metabolic disease drug targets.

Is HAYA Therapeutics a public or private company?

HAYA Therapeutics is a private company. It is classified as venture growth investor backed and is currently operating.

When was HAYA Therapeutics founded?

HAYA Therapeutics was founded in 2019. It employs 11 to 50 people.

Where is HAYA Therapeutics based?

HAYA Therapeutics is headquartered in Lausanne, Switzerland, in the Europe region.

How does HAYA Therapeutics make money?

Three revenue lines are on record. Biopharma Partnerships & Licensing (Lilly collaboration) is the primary driver. The others are venture Capital Financing (Pre-Revenue) and future Product Sales (HTX-001, pipeline).

Who are HAYA Therapeutics's main competitors?

Broad incumbents on record are BridgeBio Pharma, Alnylam Pharmaceuticals and Ionis Pharmaceuticals. Direct peers are Verve Therapeutics, Stoke Therapeutics, Tenaya Therapeutics, LEXEO Therapeutics and Dyne Therapeutics. Skyhawk Therapeutics is listed as an emerging player. Recursion Pharmaceuticals is listed as an others.

Does HAYA Therapeutics have an API?

No public API is recorded for HAYA Therapeutics.

What industry is HAYA Therapeutics in?

HAYA Therapeutics's product category is RNA-targeted Therapeutics. Its primary akta.pro industry code is HLAAADAC, Antisense Oligonucleotides (ASO) Therapeutics (splice modulation/knockdown), with a secondary code of HLAAADAG, RNA Therapeutics Platforms & Design (sequence design, target ID/validation, AI/bioinformatics). Its NAICS code is 541714 and its SIC code is 2834.

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Live signals
European BiotechnologyThe Strüngmann legacy, passed onThe Strüngmann family office launched the Strüngmann Award to recognize European biotech entrepreneurs, with a €100,000 prize. The 2026 winner is Jonathan Talbot of Mosanna and Melodia Therapeutics. The award will expand beyond Germany, Austria, and Switzerland to include more of Europe.Longevity.TechnologyHAYA’s FDA fast-track win puts heart aging in focusHAYA Therapeutics has received Fast Track designation from the US FDA for HTX-001, its investigational RNA-guided therapy for symptomatic nonobstructive hypertrophic cardiomyopathy, a condition in which scar tissue progressively stiffens the heart muscle. The therapy aims to reprogram the cells responsible for producing cardiac fibrosis rather than simply managing symptoms, representing a potential shift toward treating the underlying biology of heart disease. HTX-001 remains in Phase 1a/b clinical trials, with first participants dosed in May, and the designation enables closer FDA communication and potentially faster review pathways.startupticker.chTwo Swiss biotechs clear US regulatory steps for heart and nerve therapiesHAYA Therapeutics received FDA Fast Track designation for its cardiac fibrosis candidate HTX-001, which is in early clinical trials for hypertrophic cardiomyopathy. Oculis obtained FDA feedback supporting its plan to develop a neuroprotective candidate, Privosegtor, for multiple sclerosis relapses, with IND submission expected in late 2026.Longevity.TechnologyHAYA Therapeutics earns FDA Fast Track designation for novel heart disease therapyHAYA Therapeutics has received Fast Track designation from the U.S. FDA for HTX-001, an investigational antisense oligonucleotide therapy targeting symptomatic nonobstructive hypertrophic cardiomyopathy, a condition representing 30 to 60 percent of all HCM cases. HTX-001 is a first-in-class candidate engineered to downregulate WISPER, a heart stress-specific long non-coding RNA, to reprogram fibrotic cardiac myofibroblasts, and is currently being evaluated in a Phase 1a/b trial with the first cohort dosed in May. The Fast Track designation may enable more frequent FDA interactions and eligibility for accelerated approval, priority review, and rolling review.YahooFDA grants fast track designation for HAYA Therapeutics’ HTX-001HAYA Therapeutics has received fast track designation from the US FDA for its investigational therapy HTX-001, intended to treat symptomatic non-obstructive hypertrophic cardiomyopathy. The therapy targets a heart stress-specific lncRNA called WISPER using an antisense oligonucleotide approach designed to reprogram disease-driving cardiac fibroblasts, and is currently being evaluated in a Phase Ia/b clinical trial with the first cohort dosed in May 2025. The designation aims to expedite development and review by enabling more frequent FDA interactions and eligibility for expedited review processes.Pharmaceutical Business reviewFDA grants fast track designation for HAYA Therapeutics’ HTX-001HAYA Therapeutics has received Fast Track designation from the US FDA for its investigational therapy HTX-001, designed to treat symptomatic non-obstructive hypertrophic cardiomyopathy by targeting the heart stress-specific lncRNA WISPER. The therapy is currently being evaluated in a Phase Ia/b clinical trial, with the first cohort dosed in May 2025. The company raised $65 million in Series A funding in May 2025 to support the clinical development of HTX-001.Pharmaceutical TechnologyFDA grants fast track designation for HAYA Therapeutics’ HTX-001HAYA Therapeutics received FDA fast track designation for its experimental therapy HTX-001, targeting non-obstructive hypertrophic cardiomyopathy. The therapy, which is still under clinical trial evaluation, aims to reprogram cardiac fibroblasts to treat the disease.BioAlpsHAYA Therapeutics doses first cohort in Phase 1 trial of a precision therapy for cardiac fibrosisHAYA Therapeutics dosed the first cohort in its Phase 1 trial of HTX-001, an antisense oligonucleotide targeting WISPER, a heart stress-specific lncRNA overexpressed in hypertrophic cardiomyopathy. The trial focuses on nonobstructive hypertrophic cardiomyopathy, where current treatments do not address the underlying fibrosis. The company raised $65 million in a 2025 Series A to advance the platform.startupticker.chSwiss biotechs progress across cardiology, oncology and allergy clinical programsFour biotechs reported clinical progress: HAYA Therapeutics dosed the first cohort in a Phase 1 cardiac fibrosis trial, Mabylon reported positive Phase 1a safety for its peanut allergy candidate, Molecular Partners published Phase 1 oncology data, and Anaveon sought partners after pivoting to immunology. Anaveon's ANV600 showed early signs of activity in a Phase 1 study.Clinical Trials ArenaHAYA Therapeutics doses first cohort in Phase I HTX-001 trialHAYA Therapeutics announced full enrollment and dosing of the first cohort in its Phase I trial of HTX-001, an antisense oligonucleotide targeting Wisper, a lncRNA overexpressed in non-obstructive hypertrophic cardiomyopathy. The study will assess tolerability, safety, pharmacodynamics, and pharmacokinetics across ascending-dose cohorts in healthy volunteers and patients.