Ozmosi | Ruzinurad Drug Profile
Drug Profile
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Ruzinurad

Pronounced as: roo-ZIN-yoo-rad

Alternative Names: Ruzinurad, shr-4640, shr4640, shr 4640
Clinical Status: Active
Latest Update: 2026-04-07
Latest Update Note: Clinical Trial Update

Product Description

Jiangsu Hengrui Medicine Co is developing shr-4640, an Oral URAT1 Inhibitor for Gout; a highly selective urate transporter 1 inhibitor. (Sourced from: https://clinicaltrials.gov/ct2/show/NCT04052932; https://pubmed.ncbi.nlm.nih.gov/33693494/)

Mechanisms of Action: URAT1 Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Company: Hengrui Pharmaceutical
Company Location: Asia Pacific
Company Founding Year: 1970
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Ruzinurad

Countries in Clinic: China

Active Clinical Trial Count: 7

Recent & Upcoming Milestones

Highest Development Phases

Phase 2: Gout

Phase 1: Healthy Volunteers|Kidney Diseases

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT05954169

SHR4640-111

P1

Completed

Kidney Diseases

2024-07-01

2024-07-12

Primary Completion Date|Primary Endpoints

NCT07362355

SHR4640-204

P2

Recruiting

Gout

2027-07-01

50%

2026-04-08

Primary Endpoints|Start Date|Treatments|Trial Status

CTR20234227

CTR20234227

P1

Completed

Gout

2024-02-16

2025-04-29

CTR20233979

CTR20233979

P1

Completed

Gout

2024-01-13

2025-04-29

Patient Enrollment|Primary Completion Date|Start Date|Study Completion Date|Treatments|Trial Status

NCT06168929

SHR4640-112

P1

Completed

Healthy Volunteers

2024-01-13

2024-01-24

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

NCT06196580

SHR4640-113

P1

Completed

Gout

2024-02-16

2024-03-07

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

CTR20232161

CTR20232161

P1

Completed

Healthy Volunteers

2024-07-01

2025-04-29

Patient Enrollment|Primary Completion Date|Study Completion Date|Treatments|Trial Status