Overview

D-0120 Safety and PK/PD Study in China

Status:
Recruiting
Trial end date:
2021-12-31
Target enrollment:
Participant gender:
Summary
It is a randomized, double-blind, placebo-controlled, multiple-administration, multiple-dose, dose-escalating, phase Ib/IIa clinical study to evaluate the safety, tolerability, PK and PD of D-0120 in healthy subjects and hyperuricemia patients (gout or asymptomatic) in China.
Phase:
Phase 1/Phase 2
Details
Lead Sponsor:
InventisBio Co., Ltd
InventisBio Inc.