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Active Not RecruitingNCT05665699

Phase II Study to Evaluate Efficacy and Safety of D-0120 in Combination With Allopurinol in Subjects With Gout

A Randomized, Open-Label, Multiple-Dose Phase II Study to Evaluate Efficacy and Safety of D-0120 Administered in Combination With Allopurinol in Subjects With Gout

Status
Active Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
InventisBio Co., Ltd · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

D-0120 is being tested in combination with Allopurinol in adult subjects with Gout.

Conditions

Interventions

TypeNameDescription
DRUGD-0120increasing dose of D-0120
DRUGAllopurinolstandard dosing

Timeline

Start date
2023-04-17
Primary completion
2025-07-31
Completion
2025-12-30
First posted
2022-12-27
Last updated
2025-05-08

Locations

19 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05665699. Inclusion in this directory is not an endorsement.

Phase II Study to Evaluate Efficacy and Safety of D-0120 in Combination With Allopurinol in Subjects With Gout (NCT05665699) · Clinical Trials Directory