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A Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ABP-671 in Healthy Subjects

Gout Clinical Trial

Official title:
A Single-Center, Randomized, Double-Blind, Placebo-Controlled Phase I Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Ascending Oral Doses of ABP-671 in Healthy Volunteers in the United States

Clinical Trial Summary

The purpose of this study is to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of single ascending doses of ABP-671 administered orally in healthy volunteers.

Clinical Trial Description

Primary Objectives:

• To assess the safety and tolerability of single ascending oral doses of ABP-671 in Healthy Volunteers (HVs).

Secondary Objectives:

• To characterize the pharmacokinetics (PK) and pharmacodynamics (PD) profiles of single ascending oral doses of ABP-671 in HVs. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03906006
Study type Interventional
Source Jiangsu Atom Bioscience and Pharmaceutical Co., Ltd.
Contact
Status Completed
Phase Phase 1
Start date October 17, 2018
Completion date June 20, 2019
View Details
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