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Cyclarity Therapeutics

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uuid000ckxy

Namestring
Cyclarity Therapeutics
Legal namestring
Cyclarity Therapeutics, Inc.
Websiteurl
cyclaritytx.com
Company typeenum
Private
Founded yearint
2019
Descriptiontext

Cyclarity Therapeutics (formerly Underdog Pharmaceuticals, rebranded June 2022) is a clinical-stage biopharmaceutical company developing engineered cyclodextrin-based drugs to clear toxic oxidized cholesterol, specifically 7-ketocholesterol (7KC), a molecule implicated in atherosclerotic plaque instability and other age-related pathologies. The company was founded in 2019, is headquartered at the Buck Institute for Research on Aging in Novato, California, and operates with a 1-10 person core team supplemented by an academic and clinical collaborator network spanning Cedars-Sinai Medical Center, Monash University, and the Buck Institute.

The company's core technology is a proprietary cyclodextrin chemistry platform that selectively binds and removes 7KC from cells and tissues. Its lead asset, UDP-003, is being developed as a first-in-class treatment for atherosclerosis and entered Phase 1 clinical trials in Australia in early 2025, with results unveiled in May 2026. The pipeline extends this platform to additional indications: UDP-200 for age-related macular degeneration, UDP-300 for skin rash, and UDP-400 as a treatment-support candidate, all at the discovery stage. Drug design is supported by the in-house Cyclarity Platform and the Candymer computational chemistry suite (acquired from MD.USE in June 2020), which together run molecular dynamics simulations and docking calculations to prioritize cyclodextrin variants. The company holds a UK MHRA ILAP Innovation Passport designation for UDP-003 (granted September 2021).

Cyclarity is pre-revenue and has raised approximately $24.35M in private equity across seed (2019, Kizoo-led), Seed II (2021, Kizoo-led), bridge (2023), and Series A Tranche 1 (late 2024/early 2025, Ki Tua Fund and Starbloom Industries co-led). Its business model is currently capital-raising funded R&D with future optionality on out-licensing, co-development, or partnership monetization of UDP-003 and pipeline assets; no commercial product sales or pricing model is in place.

Short descriptiontext

Cyclarity Therapeutics is a clinical-stage biopharmaceutical company developing engineered cyclodextrin drugs that clear toxic oxidized cholesterol (7-ketocholesterol) to treat atherosclerosis and related age-related diseases. The company targets patients with cardiovascular and age-related conditions via its lead asset UDP-003 and broader pipeline.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersNovato, United States
HQ citystring
Novato
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
cardiovascular therapeutics, cyclodextrin drug development, atherosclerosis treatment, clinical-stage biopharmaceutical, oxidized cholesterol drugs
Industry2 codes
1Clinical Development (Phase I–III Trial Design & Execution)
CodeHLAIALAEPrimaryYes
2Regulatory Strategy & IND/NDA/BLA Submissions Support
CodeHLAIALAHPrimaryNo
NAICS code2 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Atherosclerosis Therapeutics
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Pharmaceutical Drug Sales
TypeOne Time License
Description

Cyclarity is a clinical-stage biopharmaceutical company developing UDP-003 for atherosclerosis and other age-related diseases. The company does not yet have revenue from product sales. Upon regulatory approval, the company plans to commercialize UDP-003 as a disease-modifying treatment for cardiovascular disease.

cyclaritytx.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

Cost components4 values
Personnel, Technology or R&D, Operations, Marketing or Sales
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Cyclarity Therapeutics is a clinical-stage biopharmaceutical company developing engineered cyclodextrin drugs to prevent and reverse age-related conditions, with lead candidate UDP-003 designed to target and remove toxic oxidized cholesterol (7-ketocholesterol) from arterial plaques. The company operates on a proprietary AI-enabled drug discovery platform (the Cyclarity Platform) that combines computational chemistry and synthetic chemistry to design cyclodextrin-based therapeutics. The company is currently conducting Phase 1 clinical trials for UDP-003 in Australia with plans for Phase 2 in 2026.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • Phase 1 trial demonstrated clear, dose-dependent urinary excretion of 7KC with no serious adverse events across dose-escalation cohorts
+2 more records
Product overview1 text field

Cyclarity Therapeutics is a clinical-stage biopharmaceutical company developing a platform of engineered cyclodextrin drugs. The core product is UDP-003, a first-in-class cyclodextrin therapeutic targeting 7-ketocholesterol (7KC) to reverse atherosclerosis. The pipeline extends to UDP-200 for macular degeneration, UDP-300 for skin rash, and UDP-400 for treatment support. All products are built on The Cyclarity Platform, a proprietary AI-enabled computational drug discovery system that enables rapid design and testing of engineered cyclodextrins targeting various hydrophobic molecules. The platform supports both the lead product and discovery-stage pipeline candidates.

Product and service1 record
1UDP-003
CategoryCardiovascular Therapeutic / Clinical-stage Pharmaceutical
Description

UDP-003 is a first-in-class engineered cyclodextrin drug candidate designed to target and remove toxic oxidized cholesterol (7-ketocholesterol / 7KC) from cells and arterial plaques. It binds directly to 7KC and facilitates urinary excretion, restoring cardiovascular self-repair function and reducing arterial plaque buildup in atherosclerosis. It is being developed for patients with atherosclerotic plaque buildup, coronary artery disease, peripheral artery disease, and carotid stenosis, with potential applications in stroke recovery, Alzheimer's disease, and Niemann Pick Type C.

Scale indicator4 records

Each record includes

Type, Value, Description, Source

Partnership6 partners
Strategic tierMinorTypeGTM or Marketing PartnerAnnounced on2025-11-03
Description

Cyclarity is listed as a partner organization in ALSAE, a nonprofit bridging longevity science and mainstream culture through partnerships with artists, filmmakers, and musicians. ALSAE aims to translate complex aging research into compelling public narratives.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-01-07
Description

Strategic partnership for Phase 1 clinical trials of UDP-003. Dr. Stephen Nicholls, Director of the Monash Victorian Heart Institute and Professor of Cardiology at Monash University, serves as lead investigator. Trial conducted at CMAX clinical research center in partnership with Monash.

Strategic tierMajorTypeStrategic or Co-development PartnerAnnounced on2023-10-17
Description

Clinical Advisory Board members Dr. Prediman K. Shah (Director of Inpatient Cardiology and Oppenheimer Atherosclerosis Research Center) and Dr. Michael E. Farkouh (Associate Dean for Research and Clinical Trials) from Cedars-Sinai. Company exploring potential lead site and primary PI roles at Cedars-Sinai for Phase 2 trials.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2022-06-24
Description

Cyclarity moved its research and operations to state-of-the-art labs at the Buck Institute for Research on Aging in Novato, California. The partnership provides access to core facilities and opportunities for collaborations with world leaders in cardiovascular disease and aging research.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2020-06-12
Description

Partnership and technology acquisition agreement. Cyclarity received ownership of Candymer molecular dynamics simulation platform and related suite of platform technologies, exclusive access to their services, and co-founders Ángel Piñeiro and Rebeca Garcia-Fandino joined the team.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2019-11-14
Description

Cyclarity was built from a SENS Research Foundation flagship program focused on addressing underlying causes of cardiovascular disease. Co-founders Matthew O'Connor and Michael Kope were formerly VP of Research and founding CEO of SRF respectively. SRF received equity, royalties, and milestones in the spinout agreement.

Recent move8 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Global biopharma with Repatha (evolocumab), the leading PCSK9 inhibitor for LDL lowering and cardiovascular risk reduction. Relevant as the broad incumbent whose franchise UDP-003 would eventually compete with or partner around in cardiovascular disease.

TypeBroad incumbent
Description

Global pharmaceutical company with Leqvio (inclisiran), an siRNA PCSK9 therapy, and a major cardiovascular franchise. Relevant broad incumbent competitor and potential acquirer/partner for next-generation disease-modifying cardiovascular therapies like UDP-003.

TypeDirect peer
Description

Specialty biopharma commercializing Vascepa (icosapent ethyl) for cardiovascular risk reduction in high-triglyceride patients. Comparable as a disease-modifying lipid therapy company pursuing outcomes-based CV indications beyond standard LDL lowering.

TypeDirect peer
Description

Late-stage clinical biopharma developing obicetrapib, a next-generation CETP inhibitor for dyslipidemia and atherosclerosis. Directly comparable as a clinical-stage lipid management company pursuing novel cardiovascular mechanisms in similar patient populations.

TypeEmerging player
Description

Clinical-stage biotech developing senolytic therapies for age-related diseases including ophthalmologic and musculoskeletal indications. Highly relevant peer given overlapping age-related disease focus, similar longevity-biotech investor base, and shared SENS Research Foundation scientific lineage.

TypeDirect peer
Description

Clinical-stage biotech developing in vivo gene editing therapies for cardiovascular disease, including PCSK9 and ANGPTL3 targets. Comparable as a disease-modifying cardiovascular company pursuing one-time interventions versus chronic lipid management, with similar patient value proposition to UDP-003.

TypeDirect peer
Description

Commercial-stage biopharma with Nexletol/Nexlizet (bempedoic acid) for LDL lowering in cardiovascular disease. Highly comparable as a lipid-management company targeting atherosclerosis with a differentiated non-statin mechanism, and relevant for benchmarking Cyclarity's eventual commercial path.

TypeEmerging player
Description

Commercial-stage RNA-targeted therapeutics company with cardiovascular pipeline assets including Lp(a)-lowering and PCSK9 programs. Comparable as a developer of novel-mechanism cardiovascular drugs targeting root-cause biology rather than systemic lipid management.

TypeDirect peer
Description

Clinical-stage biotech developing HPβCD (hydroxypropyl-beta-cyclodextrin) for Niemann-Pick Type C disease. The closest direct peer in cyclodextrin-based therapeutics, sharing chemistry platform, regulatory pathway considerations, and disease-modifying treatment philosophy for toxic accumulation diseases.

TypeDirect peer
Description

Commercial-stage biopharma with Rezdiffra (resmetirom) - the first FDA-approved treatment for MASH/NASH. Directly comparable as a developer of first-in-disease therapeutics targeting metabolic disease pathways related to toxic lipid accumulation, with potential overlap in 7KC-driven liver pathology.

Market position
Strengths5 records

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Headline, Details, Source

Weaknesses5 records

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Competitive moat4 records

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Type, Details

Key risks7 records

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Key highlights7 records

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Customer concentration

Classification, Details

Named customers1 record

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Name, Industry, Type, Use case, Source, UUID

Segment2 records

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

Ideal customer profile2 records

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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 capability2 records

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Type, Description, Source

AI maturity
App detail

Has app

Feature4 records

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Core technology
Revenue estimate
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Number of profiles
Profiles7 records

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

Subsidiaries1 record

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

Compliance1 record

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Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

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

Investors

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 →

Cyclarity Therapeutics

Atherosclerosis Therapeuticscyclaritytx.com

Cyclarity Therapeutics is a clinical-stage biopharmaceutical company developing engineered cyclodextrin drugs that clear toxic oxidized cholesterol (7-ketocholesterol) to treat atherosclerosis and related age-related diseases. The company targets patients with cardiovascular and age-related conditions via its lead asset UDP-003 and broader pipeline.

What Cyclarity Therapeutics does

Cyclarity Therapeutics (formerly Underdog Pharmaceuticals, rebranded June 2022) is a clinical-stage biopharmaceutical company developing engineered cyclodextrin-based drugs to clear toxic oxidized cholesterol, specifically 7-ketocholesterol (7KC), a molecule implicated in atherosclerotic plaque instability and other age-related pathologies. The company was founded in 2019, is headquartered at the Buck Institute for Research on Aging in Novato, California, and operates with a 1-10 person core team supplemented by an academic and clinical collaborator network spanning Cedars-Sinai Medical Center, Monash University, and the Buck Institute.

The company's core technology is a proprietary cyclodextrin chemistry platform that selectively binds and removes 7KC from cells and tissues. Its lead asset, UDP-003, is being developed as a first-in-class treatment for atherosclerosis and entered Phase 1 clinical trials in Australia in early 2025, with results unveiled in May 2026. The pipeline extends this platform to additional indications: UDP-200 for age-related macular degeneration, UDP-300 for skin rash, and UDP-400 as a treatment-support candidate, all at the discovery stage. Drug design is supported by the in-house Cyclarity Platform and the Candymer computational chemistry suite (acquired from MD.USE in June 2020), which together run molecular dynamics simulations and docking calculations to prioritize cyclodextrin variants. The company holds a UK MHRA ILAP Innovation Passport designation for UDP-003 (granted September 2021).

Cyclarity is pre-revenue and has raised approximately $24.35M in private equity across seed (2019, Kizoo-led), Seed II (2021, Kizoo-led), bridge (2023), and Series A Tranche 1 (late 2024/early 2025, Ki Tua Fund and Starbloom Industries co-led). Its business model is currently capital-raising funded R&D with future optionality on out-licensing, co-development, or partnership monetization of UDP-003 and pipeline assets; no commercial product sales or pricing model is in place.

Cyclarity Therapeutics firmographics

Firmographics
Name
Cyclarity Therapeutics
Legal name
Cyclarity Therapeutics, Inc.
Website
https://cyclaritytx.com
Company type
Private
Founded year
2019
Operating status
Operating
Headcount range
1–10 employees
Short description
Cyclarity Therapeutics is a clinical-stage biopharmaceutical company developing engineered cyclodextrin drugs that clear toxic oxidized cholesterol (7-ketocholesterol) to treat atherosclerosis and related age-related diseases. The company targets patients with cardiovascular and age-related conditions via its lead asset UDP-003 and broader pipeline.
Ownership category
akta.pro rank

Cyclarity Therapeutics industry classification

Industry
Product category
Atherosclerosis Therapeutics
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Clinical Development (Phase I–III Trial Design & Execution) (HLAIALAE)
akta.pro secondary industry
Regulatory Strategy & IND/NDA/BLA Submissions Support (HLAIALAH)

Keywords

  • Cardiovascular therapeutics
  • Cyclodextrin drug development
  • Atherosclerosis treatment
  • Clinical-stage biopharmaceutical
  • Oxidized cholesterol drugs

Where Cyclarity Therapeutics is headquartered

Location

Headquarters

HQ city
Novato
HQ country
United States
HQ region
North America

Offices2 records

Markets served

Cyclarity Therapeutics business model

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

Revenue model

  1. Pharmaceutical Drug Sales: Cyclarity is a clinical-stage biopharmaceutical company developing UDP-003 for atherosclerosis and other age-related diseases. The company does not yet have revenue from product sales. Upon regulatory approval, the company plans to commercialize UDP-003 as a disease-modifying treatment for cardiovascular disease.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels5 records

Cyclarity Therapeutics product offering

Product offering

Core offering

Cyclarity Therapeutics is a clinical-stage biopharmaceutical company developing engineered cyclodextrin drugs to prevent and reverse age-related conditions, with lead candidate UDP-003 designed to target and remove toxic oxidized cholesterol (7-ketocholesterol) from arterial plaques. The company operates on a proprietary AI-enabled drug discovery platform (the Cyclarity Platform) that combines computational chemistry and synthetic chemistry to design cyclodextrin-based therapeutics. The company is currently conducting Phase 1 clinical trials for UDP-003 in Australia with plans for Phase 2 in 2026.

Product overview

Cyclarity Therapeutics is a clinical-stage biopharmaceutical company developing a platform of engineered cyclodextrin drugs. The core product is UDP-003, a first-in-class cyclodextrin therapeutic targeting 7-ketocholesterol (7KC) to reverse atherosclerosis. The pipeline extends to UDP-200 for macular degeneration, UDP-300 for skin rash, and UDP-400 for treatment support. All products are built on The Cyclarity Platform, a proprietary AI-enabled computational drug discovery system that enables rapid design and testing of engineered cyclodextrins targeting various hydrophobic molecules. The platform supports both the lead product and discovery-stage pipeline candidates.

Differentiator

Problem solved

Functional benefit

Products and services

  • UDP-003 UDP-003 is a first-in-class engineered cyclodextrin drug candidate designed to target and remove toxic oxidized cholesterol (7-ketocholesterol / 7KC) from cells and arterial plaques. It binds directly to 7KC and facilitates urinary excretion, restoring cardiovascular self-repair function and reducing arterial plaque buildup in atherosclerosis. It is being developed for patients with atherosclerotic plaque buildup, coronary artery disease, peripheral artery disease, and carotid stenosis, with potential applications in stroke recovery, Alzheimer's disease, and Niemann Pick Type C.

Quantifiable outcome

  • Phase 1 trial demonstrated clear, dose-dependent urinary excretion of 7KC with no serious adverse events across dose-escalation cohorts
  • +2 more outcomes

Companies that use Cyclarity Therapeutics

Customer profile

Named customers1 record

Segments2 records

Ideal customer profiles2 records

Cyclarity Therapeutics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability2 records

Feature4 records

Cyclarity Therapeutics partnerships and signals

Strategic signal

Partnerships

Six partnerships are on record, tiered minor, core and major.

  • Alliance for Longevity Science, Arts & Entertainment (ALSAE)minorGTM or Marketing Partner · 3 November 2025Cyclarity is listed as a partner organization in ALSAE, a nonprofit bridging longevity science and mainstream culture through partnerships with artists, filmmakers, and musicians. ALSAE aims to translate complex aging research into compelling public narratives.
  • Monash University / Monash Victorian Heart InstitutecoreStrategic or Co-development Partner · 7 January 2025Strategic partnership for Phase 1 clinical trials of UDP-003. Dr. Stephen Nicholls, Director of the Monash Victorian Heart Institute and Professor of Cardiology at Monash University, serves as lead investigator. Trial conducted at CMAX clinical research center in partnership with Monash.
  • Cedars-Sinai HospitalmajorStrategic or Co-development Partner · 17 October 2023Clinical Advisory Board members Dr. Prediman K. Shah (Director of Inpatient Cardiology and Oppenheimer Atherosclerosis Research Center) and Dr. Michael E. Farkouh (Associate Dean for Research and Clinical Trials) from Cedars-Sinai. Company exploring potential lead site and primary PI roles at Cedars-Sinai for Phase 2 trials.
  • Buck Institute for Research on AgingcoreStrategic or Co-development Partner · 24 June 2022Cyclarity moved its research and operations to state-of-the-art labs at the Buck Institute for Research on Aging in Novato, California. The partnership provides access to core facilities and opportunities for collaborations with world leaders in cardiovascular disease and aging research.
  • MD.USE Innovative Solutions, SLcoreTechnology or Integration · 12 June 2020Partnership and technology acquisition agreement. Cyclarity received ownership of Candymer molecular dynamics simulation platform and related suite of platform technologies, exclusive access to their services, and co-founders Ángel Piñeiro and Rebeca Garcia-Fandino joined the team.
  • SENS Research FoundationcoreStrategic or Co-development Partner · 14 November 2019Cyclarity was built from a SENS Research Foundation flagship program focused on addressing underlying causes of cardiovascular disease. Co-founders Matthew O'Connor and Michael Kope were formerly VP of Research and founding CEO of SRF respectively. SRF received equity, royalties, and milestones in the spinout agreement.

Scale indicators4 records

Recent moves8 records

Expansion highlights5 records

Cyclarity Therapeutics competitors and assessment

Company assessment

Broad incumbents

  • Amgen: Global biopharma with Repatha (evolocumab), the leading PCSK9 inhibitor for LDL lowering and cardiovascular risk reduction. Relevant as the broad incumbent whose franchise UDP-003 would eventually compete with or partner around in cardiovascular disease.
  • Novartis: Global pharmaceutical company with Leqvio (inclisiran), an siRNA PCSK9 therapy, and a major cardiovascular franchise. Relevant broad incumbent competitor and potential acquirer/partner for next-generation disease-modifying cardiovascular therapies like UDP-003.

Direct peers

  • Amarin Corporation: Specialty biopharma commercializing Vascepa (icosapent ethyl) for cardiovascular risk reduction in high-triglyceride patients. Comparable as a disease-modifying lipid therapy company pursuing outcomes-based CV indications beyond standard LDL lowering.
  • NewAmsterdam Pharma: Late-stage clinical biopharma developing obicetrapib, a next-generation CETP inhibitor for dyslipidemia and atherosclerosis. Directly comparable as a clinical-stage lipid management company pursuing novel cardiovascular mechanisms in similar patient populations.
  • Verve Therapeutics: Clinical-stage biotech developing in vivo gene editing therapies for cardiovascular disease, including PCSK9 and ANGPTL3 targets. Comparable as a disease-modifying cardiovascular company pursuing one-time interventions versus chronic lipid management, with similar patient value proposition to UDP-003.
  • Esperion Therapeutics: Commercial-stage biopharma with Nexletol/Nexlizet (bempedoic acid) for LDL lowering in cardiovascular disease. Highly comparable as a lipid-management company targeting atherosclerosis with a differentiated non-statin mechanism, and relevant for benchmarking Cyclarity's eventual commercial path.
  • Mandos LLC: Clinical-stage biotech developing HPβCD (hydroxypropyl-beta-cyclodextrin) for Niemann-Pick Type C disease. The closest direct peer in cyclodextrin-based therapeutics, sharing chemistry platform, regulatory pathway considerations, and disease-modifying treatment philosophy for toxic accumulation diseases.
  • Madrigal Pharmaceuticals: Commercial-stage biopharma with Rezdiffra (resmetirom) - the first FDA-approved treatment for MASH/NASH. Directly comparable as a developer of first-in-disease therapeutics targeting metabolic disease pathways related to toxic lipid accumulation, with potential overlap in 7KC-driven liver pathology.

Emerging players

  • Unity Biotechnology: Clinical-stage biotech developing senolytic therapies for age-related diseases including ophthalmologic and musculoskeletal indications. Highly relevant peer given overlapping age-related disease focus, similar longevity-biotech investor base, and shared SENS Research Foundation scientific lineage.
  • Ionis Pharmaceuticals: Commercial-stage RNA-targeted therapeutics company with cardiovascular pipeline assets including Lp(a)-lowering and PCSK9 programs. Comparable as a developer of novel-mechanism cardiovascular drugs targeting root-cause biology rather than systemic lipid management.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks7 records

Key highlights7 records

Customer concentration

Cyclarity Therapeutics social profiles

Digital presence

Cyclarity Therapeutics compliance and trust

Trust signal

Compliance1 record

Cyclarity Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Cyclarity Therapeutics leadership team

Management profile

Number of profiles

Profiles7 records

Cyclarity Therapeutics subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

Cyclarity Therapeutics funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Cyclarity 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 Cyclarity Therapeutics

What does Cyclarity Therapeutics do?

Cyclarity Therapeutics is a clinical-stage biopharmaceutical company developing engineered cyclodextrin drugs to prevent and reverse age-related conditions, with lead candidate UDP-003 designed to target and remove toxic oxidized cholesterol (7-ketocholesterol) from arterial plaques. The company operates on a proprietary AI-enabled drug discovery platform (the Cyclarity Platform) that combines computational chemistry and synthetic chemistry to design cyclodextrin-based therapeutics. The company is currently conducting Phase 1 clinical trials for UDP-003 in Australia with plans for Phase 2 in 2026.

Is Cyclarity Therapeutics a public or private company?

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

When was Cyclarity Therapeutics founded?

Cyclarity Therapeutics was founded in 2019. It employs 1 to 10 people.

Where is Cyclarity Therapeutics based?

Cyclarity Therapeutics is headquartered in Novato, United States, in the North America region.

How does Cyclarity Therapeutics make money?

One revenue line is on record: pharmaceutical Drug Sales.

Who are Cyclarity Therapeutics's main competitors?

Broad incumbents on record are Amgen and Novartis. Direct peers are Amarin Corporation, NewAmsterdam Pharma, Verve Therapeutics, Esperion Therapeutics, Mandos LLC and Madrigal Pharmaceuticals. Emerging players are Unity Biotechnology and Ionis Pharmaceuticals.

Does Cyclarity Therapeutics have an API?

No public API is recorded for Cyclarity Therapeutics.

What industry is Cyclarity Therapeutics in?

Cyclarity Therapeutics's product category is Atherosclerosis Therapeutics. Its primary akta.pro industry code is HLAIALAE, Clinical Development (Phase I–III Trial Design & Execution), with a secondary code of HLAIALAH, Regulatory Strategy & IND/NDA/BLA Submissions Support. Its NAICS code is 541714 and its SIC code is 2834.

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Live signals
Longevity.TechnologyCyclarity’s lead drug successfully clears toxic cholesterol in Phase 1 trialCyclarity presented Phase 1 data for UDP-003 at the American Heart Association Vascular Discovery Scientific Sessions, showing dose-dependent urinary excretion of 7-ketocholesterol with no serious adverse events. The drug has a short half-life and linear pharmacokinetics, and Cyclarity expects to initiate a Phase 2 trial later in 2026.LifespanThe Many Dangers of 7-KetocholesterolResearchers, including Matthew O’Connor of Cyclarity Therapeutics, published a review detailing the harmful effects of 7-ketocholesterol (7KC) on human health, linking it to cardiovascular disease and neuronal damage. The article highlights that while current treatments are limited, Cyclarity Therapeutics is developing UDP-003, a cyclodextrin-based drug currently in Phase 1 clinical trials to target and remove 7KC from cells.Longevity.TechnologyArt meets science to tackle diseases of agingThe Alliance for Longevity Science, Arts & Entertainment (ALSAE) has launched as a nonprofit to bridge the gap between longevity science and mainstream culture by partnering with artists, filmmakers, and musicians to translate complex aging research into compelling public narratives. The organization, whose founding partners include XPRIZE Healthspan, the Aoki Foundation, and the Buck Institute for Research on Aging, plans to host private retreats for Hollywood showrunners at leading longevity research centers starting next year. ALSAE's partner organizations include biotech companies Cyclarity Therapeutics, Kimera Labs, and Intervene Immune, as well as Methuselah Foundation as its fiscal sponsor.