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Atom Therapeutics Co

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uuid003lxga

Namestring
Atom Therapeutics Co
Legal namestring
Atom Therapeutics Co., Ltd
Websiteurl
atomthera.us
Company typeenum
Private
Founded yearint
2012
Descriptiontext

Atom Therapeutics Co., Ltd is a privately held, clinical-stage biotechnology company founded in March 2012 by Dr. William (Dongfang) Shi as Atom Bioscience, subsequently rebranded in November 2024. Headquartered in Hangzhou, China, with additional offices in Suzhou, China and Newark, California (Atom Therapeutics America, Inc.), the company employs 11–50 staff and has raised approximately $170 million USD across multiple venture rounds, including an $83 million Series D led by Kaitai Capital in October 2023.

The company's core pipeline consists of small-molecule therapeutics for inflammatory, metabolic, and cardiovascular diseases. Its lead asset is ABP-671 (lingdolinurad), a patented URAT1 inhibitor designed as a once-daily oral tablet for chronic gout and hyperuricemia, currently in global Phase 3 trials synchronized between the US and China (with the first Chinese Phase 3 patient dosed in June 2026). ABP-745 is a novel anti-inflammatory small molecule in Phase 2 development for both acute gout flares and, as of FDA approval in December 2025, atherosclerotic cardiovascular disease (ASCVD). Earlier-stage candidates include ABP-6118, a xanthine oxidase inhibitor for gout, and ABP-431, an anticancer compound.

Atom Therapeutics is pre-revenue and operates a licensing-driven commercial model. In December 2024, it granted China Medical System Holdings Ltd (CMS) exclusive commercialization rights to lingdolinurad in mainland China, Hong Kong, and Macao, while retaining development and commercialization rights for other global markets. Forward commercialization in those retained geographies is planned through direct sales or additional partnerships, supported by business-development outreach at major industry events such as BIO-Europe 2025.

Short descriptiontext

Atom Therapeutics is a clinical-stage Chinese-American biotechnology company developing patented small-molecule drugs — led by URAT1 inhibitor lingdolinurad for chronic gout and ABP-745 for acute gout and ASCVD — through synchronized US and China Phase 2/3 trials for global commercialization.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersHangzhou, China
HQ citystring
Hangzhou
HQ countrystring
China
HQ regionstring
Asia
Markets served

Serves global market

Offices3 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
small molecule drugs, gout therapeutics, hyperuricemia treatment, anti-inflammatory drugs, clinical-stage biopharmaceuticals
NAICS code1 code
  • Pharmaceutical and Medicine Manufacturing3254
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Clinical-Stage Biopharmaceuticals
Social media profiles2 records
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model2 records
1Pharmaceutical Product Sales
TypeOne Time License
Description

Pre-revenue clinical stage company. Expected future revenue from sales of ABP-671 for chronic gout and ABP-745 for acute gout upon regulatory approval.

atomthera.us
2Licensing and Commercialization Rights
TypeLicensing Royalties
Description

Licensing deal with China Medical System Holdings for exclusive commercialization rights to lingdolinurad in China, Hong Kong, and Macao. Company retains global rights outside these territories.

atomthera.us
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

Each record includes

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

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

Atom Therapeutics Co is a clinical-stage biopharmaceutical company developing proprietary small molecule drug candidates for inflammatory, metabolic, and cardiovascular diseases. Its lead asset, ABP-671 (lingdolinurad), is a URAT1 inhibitor in global Phase 3 trials for chronic gout and hyperuricemia, while ABP-745 is an anti-inflammatory drug in Phase 2 trials for acute gout and atherosclerotic cardiovascular disease (ASCVD). The company licenses and commercializes its drug candidates through partnerships such as China Medical System Holdings in Greater China.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Atom Therapeutics is a clinical-stage biotechnology company developing a portfolio of best-in-class small molecule drugs for inflammatory, metabolic, and cardiovascular diseases. The company's lead product is ABP-671 (lingdolinurad), a URAT1 inhibitor in global Phase 3 trials for chronic gout and hyperuricemia. ABP-745 is a novel anti-inflammatory agent in Phase 2 trials for acute gout and atherosclerotic cardiovascular disease (ASCVD). The pipeline also includes ABP-6118 (xanthine oxidase inhibitor for gout) and ABP-431 (anticancer), both in earlier stages. The company pursues a synchronized development strategy with trials ongoing in both China and the US.

Product and service4 records
1ABP-671 (Lingdolinurad)
CategorySmall Molecule Drug
Description

A URAT1 inhibitor small molecule drug for chronic gout and hyperuricemia, administered once daily as an oral tablet. Reduces uric acid reabsorption in the kidneys, increases urinary excretion to lower serum uric acid levels, reduces tophi size, and prevents gout attacks. Currently in global Phase 3 trials.

2ABP-745
CategorySmall Molecule Drug
Description

A novel anti-inflammatory small molecule drug for acute gout and atherosclerotic cardiovascular disease (ASCVD). Demonstrated higher safety and tolerability compared to existing acute gout treatments like colchicine and NSAIDs. In Phase 2 trials for acute gout flares and ASCVD.

3ABP-6118
CategorySmall Molecule Drug
Description

A xanthine oxidase inhibitor small molecule drug in preclinical development for gout treatment.

4ABP-431
Scale indicator9 records

Each record includes

Type, Value, Description, Source

Partnership2 partners
Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2024-12-01
Description

Exclusive commercialization agreement for lingdolinurad (ABP-671) to treat chronic gout and hyperuricemia. CMS obtained exclusive rights to commercialize the drug across mainland China, Hong Kong, and Macao. Atom Therapeutics retains rights for other global markets.

Strategic tierMinorTypeGTM or Marketing Partner
Description

Atom Therapeutics joined Gout Education Society on Gout Awareness Day (May 22) to help educate the public on risk factors and treatment options for gout.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeRegional player
Description

Leading Chinese clinical CRO and emerging biopharma sponsor, comparable as a Hangzhou-headquartered clinical-stage drug developer operating in the same regulatory and capital environment as Atom Therapeutics.

TypeDirect peer
Description

Japanese specialty pharma that developed and markets dotinurad (URECE), a URAT1 inhibitor for gout and hyperuricemia — the most directly competitive commercialized molecule to ABP-671, addressing the same target and indication.

TypeBroad incumbent
Description

Developed oral small-molecule therapies for inflammatory diseases (e.g., TAVNEOS for ANCA-associated vasculitis), making it a broadly comparable late-stage small-molecule inflammation biotech that was ultimately acquired by a large pharma.

TypeRegional player
Description

Korean specialty pharma with a URAT1 inhibitor (URICONT/lesinurad) franchise for gout, making it a regionally focused peer competing in Asia with a similar mechanism of action to ABP-671.

TypeEmerging player
Description

Clinical-stage US biotech developing oral small-molecule therapies for metabolic and inflammatory diseases — comparable in development stage, modality, and therapeutic area focus to Atom Therapeutics.

TypeBroad incumbent
Description

Late-stage clinical biotech that developed resmetirom (Rezdiffra), an oral small-molecule therapy for metabolic liver disease — comparable in being a clinical-to-commercial small-molecule company targeting metabolic and inflammatory conditions.

TypeBroad incumbent
Description

Marketed Krystexxa (pegloticase) for refractory chronic gout, making it a relevant commercial-stage peer in the gout therapeutic area, though addressing a different (refractory) patient segment than ABP-671's first-line positioning.

TypeRegional player
Description

Major Chinese clinical-to-commercial biopharma with a strong gout/urate-lowering pipeline including a URAT1 inhibitor, making it a directly relevant China-based peer targeting the same indication as ABP-671.

TypeDirect peer
Description

Developed lesinurad (Zurampic), a URAT1 inhibitor approved for chronic gout, providing direct mechanistic and clinical comparability to ABP-671, though lesinurad was ultimately withdrawn for renal safety — a key cautionary data point for the class.

TypeDirect peer
Description

Developed and markets febuxostat (Feburic), a leading branded oral urate-lowering therapy for chronic gout, making it a direct global competitor that ABP-671 must clinically differentiate against in efficacy and safety.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 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 highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment4 records

Each record includes

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

Ideal customer profile3 records

Each record includes

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

Technology focused
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
Profiles1 record

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 rounds

Each record includes

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 →

Atom Therapeutics Co

Clinical-Stage Biopharmaceuticalsatomthera.us

Atom Therapeutics is a clinical-stage Chinese-American biotechnology company developing patented small-molecule drugs — led by URAT1 inhibitor lingdolinurad for chronic gout and ABP-745 for acute gout and ASCVD — through synchronized US and China Phase 2/3 trials for global commercialization.

What Atom Therapeutics Co does

Atom Therapeutics Co., Ltd is a privately held, clinical-stage biotechnology company founded in March 2012 by Dr. William (Dongfang) Shi as Atom Bioscience, subsequently rebranded in November 2024. Headquartered in Hangzhou, China, with additional offices in Suzhou, China and Newark, California (Atom Therapeutics America, Inc.), the company employs 11–50 staff and has raised approximately $170 million USD across multiple venture rounds, including an $83 million Series D led by Kaitai Capital in October 2023.

The company's core pipeline consists of small-molecule therapeutics for inflammatory, metabolic, and cardiovascular diseases. Its lead asset is ABP-671 (lingdolinurad), a patented URAT1 inhibitor designed as a once-daily oral tablet for chronic gout and hyperuricemia, currently in global Phase 3 trials synchronized between the US and China (with the first Chinese Phase 3 patient dosed in June 2026). ABP-745 is a novel anti-inflammatory small molecule in Phase 2 development for both acute gout flares and, as of FDA approval in December 2025, atherosclerotic cardiovascular disease (ASCVD). Earlier-stage candidates include ABP-6118, a xanthine oxidase inhibitor for gout, and ABP-431, an anticancer compound.

Atom Therapeutics is pre-revenue and operates a licensing-driven commercial model. In December 2024, it granted China Medical System Holdings Ltd (CMS) exclusive commercialization rights to lingdolinurad in mainland China, Hong Kong, and Macao, while retaining development and commercialization rights for other global markets. Forward commercialization in those retained geographies is planned through direct sales or additional partnerships, supported by business-development outreach at major industry events such as BIO-Europe 2025.

Atom Therapeutics Co firmographics

Firmographics
Name
Atom Therapeutics Co
Legal name
Atom Therapeutics Co., Ltd
Website
https://atomthera.us
Company type
Private
Founded year
2012
Operating status
Operating
Headcount range
11–50 employees
Short description
Atom Therapeutics is a clinical-stage Chinese-American biotechnology company developing patented small-molecule drugs — led by URAT1 inhibitor lingdolinurad for chronic gout and ABP-745 for acute gout and ASCVD — through synchronized US and China Phase 2/3 trials for global commercialization.
Ownership category
akta.pro rank

Where Atom Therapeutics Co is headquartered

Location

Headquarters

HQ city
Hangzhou
HQ country
China
HQ region
Asia

Offices3 records

Markets served

Atom Therapeutics Co business model

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

Revenue model

  1. Pharmaceutical Product Sales: Pre-revenue clinical stage company. Expected future revenue from sales of ABP-671 for chronic gout and ABP-745 for acute gout upon regulatory approval.
  2. Licensing and Commercialization Rights: Licensing deal with China Medical System Holdings for exclusive commercialization rights to lingdolinurad in China, Hong Kong, and Macao. Company retains global rights outside these territories.

Go-to-market motion2 records

Distribution channels2 records

Marketing channels5 records

Atom Therapeutics Co product offering

Product offering

Core offering

Atom Therapeutics Co is a clinical-stage biopharmaceutical company developing proprietary small molecule drug candidates for inflammatory, metabolic, and cardiovascular diseases. Its lead asset, ABP-671 (lingdolinurad), is a URAT1 inhibitor in global Phase 3 trials for chronic gout and hyperuricemia, while ABP-745 is an anti-inflammatory drug in Phase 2 trials for acute gout and atherosclerotic cardiovascular disease (ASCVD). The company licenses and commercializes its drug candidates through partnerships such as China Medical System Holdings in Greater China.

Product overview

Atom Therapeutics is a clinical-stage biotechnology company developing a portfolio of best-in-class small molecule drugs for inflammatory, metabolic, and cardiovascular diseases. The company's lead product is ABP-671 (lingdolinurad), a URAT1 inhibitor in global Phase 3 trials for chronic gout and hyperuricemia. ABP-745 is a novel anti-inflammatory agent in Phase 2 trials for acute gout and atherosclerotic cardiovascular disease (ASCVD). The pipeline also includes ABP-6118 (xanthine oxidase inhibitor for gout) and ABP-431 (anticancer), both in earlier stages. The company pursues a synchronized development strategy with trials ongoing in both China and the US.

Differentiator

Problem solved

Functional benefit

Products and services

  • ABP-671 (Lingdolinurad) A URAT1 inhibitor small molecule drug for chronic gout and hyperuricemia, administered once daily as an oral tablet. Reduces uric acid reabsorption in the kidneys, increases urinary excretion to lower serum uric acid levels, reduces tophi size, and prevents gout attacks. Currently in global Phase 3 trials.
  • ABP-745 A novel anti-inflammatory small molecule drug for acute gout and atherosclerotic cardiovascular disease (ASCVD). Demonstrated higher safety and tolerability compared to existing acute gout treatments like colchicine and NSAIDs. In Phase 2 trials for acute gout flares and ASCVD.
  • ABP-6118 A xanthine oxidase inhibitor small molecule drug in preclinical development for gout treatment.
  • ABP-431

Companies that use Atom Therapeutics Co

Customer profile

Segments4 records

Ideal customer profiles3 records

Atom Therapeutics Co technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Atom Therapeutics Co partnerships and signals

Strategic signal

Partnerships

Two partnerships are on record, tiered core and minor.

  • China Medical System Holdings Ltd (CMS)coreChannel Partner/ Reseller/ Distributor · 1 December 2024Exclusive commercialization agreement for lingdolinurad (ABP-671) to treat chronic gout and hyperuricemia. CMS obtained exclusive rights to commercialize the drug across mainland China, Hong Kong, and Macao. Atom Therapeutics retains rights for other global markets.
  • Gout Education SocietyminorGTM or Marketing PartnerAtom Therapeutics joined Gout Education Society on Gout Awareness Day (May 22) to help educate the public on risk factors and treatment options for gout.

Scale indicators9 records

Recent moves7 records

Expansion highlights6 records

Atom Therapeutics Co competitors and assessment

Company assessment

Regional players

  • Tigermed: Leading Chinese clinical CRO and emerging biopharma sponsor, comparable as a Hangzhou-headquartered clinical-stage drug developer operating in the same regulatory and capital environment as Atom Therapeutics.
  • JW Pharmaceutical: Korean specialty pharma with a URAT1 inhibitor (URICONT/lesinurad) franchise for gout, making it a regionally focused peer competing in Asia with a similar mechanism of action to ABP-671.
  • Innovent Biologics: Major Chinese clinical-to-commercial biopharma with a strong gout/urate-lowering pipeline including a URAT1 inhibitor, making it a directly relevant China-based peer targeting the same indication as ABP-671.

Direct peers

  • Kissei Pharmaceutical: Japanese specialty pharma that developed and markets dotinurad (URECE), a URAT1 inhibitor for gout and hyperuricemia — the most directly competitive commercialized molecule to ABP-671, addressing the same target and indication.
  • Ardea Biosciences (AstraZeneca): Developed lesinurad (Zurampic), a URAT1 inhibitor approved for chronic gout, providing direct mechanistic and clinical comparability to ABP-671, though lesinurad was ultimately withdrawn for renal safety — a key cautionary data point for the class.
  • Teijin Pharma: Developed and markets febuxostat (Feburic), a leading branded oral urate-lowering therapy for chronic gout, making it a direct global competitor that ABP-671 must clinically differentiate against in efficacy and safety.

Broad incumbents

  • ChemoCentryx (Amgen): Developed oral small-molecule therapies for inflammatory diseases (e.g., TAVNEOS for ANCA-associated vasculitis), making it a broadly comparable late-stage small-molecule inflammation biotech that was ultimately acquired by a large pharma.
  • Madrigal Pharmaceuticals: Late-stage clinical biotech that developed resmetirom (Rezdiffra), an oral small-molecule therapy for metabolic liver disease — comparable in being a clinical-to-commercial small-molecule company targeting metabolic and inflammatory conditions.
  • Horizon Therapeutics (Amgen): Marketed Krystexxa (pegloticase) for refractory chronic gout, making it a relevant commercial-stage peer in the gout therapeutic area, though addressing a different (refractory) patient segment than ABP-671's first-line positioning.

Emerging players

  • Viking Therapeutics: Clinical-stage US biotech developing oral small-molecule therapies for metabolic and inflammatory diseases — comparable in development stage, modality, and therapeutic area focus to Atom Therapeutics.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat4 records

Key risks6 records

Key highlights6 records

Customer concentration

Atom Therapeutics Co social profiles

Digital presence

Atom Therapeutics Co financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Atom Therapeutics Co leadership team

Management profile

Number of profiles

Profiles1 record

Atom Therapeutics Co funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Atom Therapeutics Co 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 Atom Therapeutics Co

What does Atom Therapeutics Co do?

Atom Therapeutics Co is a clinical-stage biopharmaceutical company developing proprietary small molecule drug candidates for inflammatory, metabolic, and cardiovascular diseases. Its lead asset, ABP-671 (lingdolinurad), is a URAT1 inhibitor in global Phase 3 trials for chronic gout and hyperuricemia, while ABP-745 is an anti-inflammatory drug in Phase 2 trials for acute gout and atherosclerotic cardiovascular disease (ASCVD). The company licenses and commercializes its drug candidates through partnerships such as China Medical System Holdings in Greater China.

Is Atom Therapeutics Co a public or private company?

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

When was Atom Therapeutics Co founded?

Atom Therapeutics Co was founded in 2012. It employs 11 to 50 people.

Where is Atom Therapeutics Co based?

Atom Therapeutics Co is headquartered in Hangzhou, China, in the Asia region.

How does Atom Therapeutics Co make money?

Two revenue lines are on record. Pharmaceutical Product Sales are the primary driver. The others are licensing and Commercialization Rights.

Who are Atom Therapeutics Co's main competitors?

Regional players on record are Tigermed, JW Pharmaceutical and Innovent Biologics. Direct peers are Kissei Pharmaceutical, Ardea Biosciences (AstraZeneca) and Teijin Pharma. Broad incumbents are ChemoCentryx (Amgen), Madrigal Pharmaceuticals and Horizon Therapeutics (Amgen). Viking Therapeutics is listed as an emerging player.

Does Atom Therapeutics Co have an API?

No public API is recorded for Atom Therapeutics Co.

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Live signals
FinancialContent Business PageAtom Therapeutics Announces First Patient Dosed in China Phase 3 Clinical Trial of Lingdolinurad (ABP-671) for Chronic GoutAtom Therapeutics announced the first patient has been dosed in its China Phase 3 clinical trial for lingdolinurad (ABP-671), an investigational drug for chronic gout, with plans to enroll more than 800 patients in a multicenter study comparing the drug against febuxostat. Phase 2b data demonstrated that lingdolinurad achieved serum uric acid levels below 6 mg/dL in over 91% of subjects after 8 weeks of dosing, showed ability to eliminate tophi in some patients within 6 months, and reduced acute gout attack incidence by 67% compared to placebo in US trials. The company is pursuing a synchronized development strategy with both China and US Phase 3 trials underway, as it seeks regulatory approval to address the needs of over 60 million gout patients and 300 million individuals with hyperuricemia worldwide.MorningstarAtom Therapeutics Announces First Patient Dosed in China Phase 3 Clinical Trial of Lingdolinurad (ABP-671) for Chronic GoutAtom Therapeutics announced the first patient dosed in its China Phase 3 trial of lingdolinurad (ABP-671) for chronic gout. The multicenter, randomized, double-blind trial will enroll over 800 patients and compare lingdolinurad with febuxostat. Results are expected to support regulatory submissions for marketing approval in China.Business Wire BlogAtom Therapeutics Announces First Patient Dosed in China Phase 3 Clinical Trial of Lingdolinurad (ABP-671) for Chronic GoutAtom Therapeutics announced the first patient dosed in its Phase 3 China trial of lingdolinurad (ABP-671) for chronic gout. The trial will enroll over 800 patients and compare the drug to febuxostat, with results expected to support regulatory submissions. The US Phase 3 program is planned for initiation later this year.openPR.comHyperuricemia Clinical Trial Analysis 2026: 15+ Companies Advancing 20+ Therapies Across Clinical Stages, Driving Next-Gen Treatment Innovations | DelveInsightDelveInsight released its 2026 Hyperuricemia Pipeline report identifying 15+ companies developing 20+ therapies across various clinical stages for the treatment of hyperuricemia, a condition characterized by elevated uric acid levels that can lead to gout or kidney stones. In March 2025, Shanton Pharma reported promising Phase 2b results for its novel urate-lowering therapy SAP-001, claiming "best in class" outcomes for patients unresponsive to standard xanthine oxidase inhibitor treatments. In December 2024, Atom Therapeutics entered into an exclusive commercialization agreement with China Medical System Holdings Ltd (CMS) to commercialize lingdolinurad (ABP-671) for chronic gout and hyperuricemia across mainland China, Hong Kong, and Macao.PharmiWeb.comAtom Therapeutics Launches Multi-Regional Phase 2 Trial of ABP-745 for Atherosclerotic Cardiovascular Disease (ASCVD)Atom Therapeutics announced FDA approval and launch of a multi-regional Phase II clinical trial for ABP-745, a novel oral anti-inflammatory agent targeting atherosclerosis, a disease responsible for approximately 18 million deaths annually worldwide. ABP-745 demonstrated a significantly wider therapeutic safety window compared to colchicine in animal studies, with up to 56.1% reduction in aortic plaque area and over 75% reduction when combined with statins, while also eliminating drug-drug interaction risks. The drug has completed favorable Phase I trials in the U.S. and China, with a separate multi-regional Phase II trial for acute gout flares already underway across the U.S., Australia, and China.PharmiWeb.comAtom Therapeutics to Present Positive Data from Clinical Trials of Its Lead Novel Oral Drugs for Chronic Gout and Acute Gout Flares at ACR Convergence 2025Atom Therapeutics announced it will present positive Phase 2a data for lingdolinurad (ABP-671) in chronic gout patients with mild-to-moderate renal impairment at ACR Convergence 2025, demonstrating dose-dependent serum uric acid reduction below the 6 mg/dL therapeutic target with good safety and tolerability. The company also reported positive Phase 1 results for ABP-745, an anti-inflammatory drug for acute gout flares, showing good safety and pharmacokinetics in healthy volunteers, supporting advancement to a multi-country Phase 2 trial comparing the drug to placebo and colchicine.