Status:

COMPLETED

The Study is Designed to Evaluate Single Ascending Doses of AR882 in Healthy Adult Males

Lead Sponsor:

Arthrosi Therapeutics

Conditions:

Healthy Volunteers

Eligibility:

MALE

18-55 years

Phase:

PHASE1

Brief Summary

A randomized, double-blind, placebo-controlled, single ascending dose study of AR882 in healthy adult males.

Eligibility Criteria

Inclusion

  • Serum uric acid level ≥ 4.5 mg/dL (268 µmol/L)
  • Body weight no less than 50 kg and body mass index (BMI) within the range of ≥18 and ≤33 kg/m2
  • Must be free of any clinically significant disease that requires a physician's care and/or would interfere with study evaluations or procedures

Exclusion

  • Malignancy within 5 years, except for successfully treated basal or squamous cell carcinoma of the skin
  • History of cardiac abnormalities
  • History and/or presence of drug addiction or excessive use of alcohol

Key Trial Info

Start Date :

January 22 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

July 31 2019

Estimated Enrollment :

64 Patients enrolled

Trial Details

Trial ID

NCT04347005

Start Date

January 22 2019

End Date

July 31 2019

Last Update

November 16 2020

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Nucleus Network Pty, Ltd.

Melbourne, Victoria, Australia, 3004

The Study is Designed to Evaluate Single Ascending Doses of AR882 in Healthy Adult Males | DecenTrialz