Cyclarity Therapeutics
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.
- Company typePrivate
- Founded2019
- HeadquartersNovato, United States
- Headcount1–10
- GTM typeB2B
- OfferingHardware or Manufacturing
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
Where Cyclarity Therapeutics is headquartered
LocationHeadquarters
- 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
- 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 offeringCore 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 profileNamed customers1 record
Segments2 records
Ideal customer profiles2 records
Cyclarity Therapeutics technology and API
TechnologyTechnology 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 signalPartnerships
Six partnerships are on record, tiered minor, core and major.
- Alliance for Longevity Science, Arts & Entertainment (ALSAE)minorCyclarity 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 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 HospitalmajorClinical 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 AgingcoreCyclarity 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, SLcorePartnership 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 FoundationcoreCyclarity 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 assessmentBroad 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 presenceCyclarity Therapeutics compliance and trust
Trust signalCompliance1 record
Cyclarity Therapeutics financial estimates
Financial estimateRevenue estimate
Valuation estimate
Cyclarity Therapeutics leadership team
Management profileNumber of profiles
Profiles7 records
Cyclarity Therapeutics subsidiaries and ownership
Company hierarchySubsidiaries1 record
Cyclarity Therapeutics funding detail
Funding detailFunding 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 investmentM&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.