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Clinical Trials/NCT03015948
NCT03015948
Completed
Phase 1

A Phase I Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Dose of SHR4640 in Healthy Male Volunteers

Atridia Pty Ltd.1 site in 1 country40 target enrollmentSeptember 22, 2016
ConditionsGout
InterventionsSHR4640Placebo

Overview

Phase
Phase 1
Intervention
SHR4640
Conditions
Gout
Sponsor
Atridia Pty Ltd.
Enrollment
40
Locations
1
Primary Endpoint
Assess safety and tolerability of SHR 4640 over 11days including AEs, laboratory safety variables (including hematology, creatinine kinase (CK), biochemistry, and urinalysis), physical examinations, vital signs, and 12-lead electrocardiograms (ECGs)
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

This is a single-center, randomized, double-blind, placebo-controlled, single ascending-dose Phase I trial.

Detailed Description

This study includes screening (Days -16 to -3), check-in (Day -2), enrollment (Day -1), dosing (Day 1), observational period (Days 2 to 3), discharge day (Day 4), and safety follow-up visit (Day 8). Forty eligible subjects will be enrolled into 4 dose cohorts (10 for each cohort), and every 10 subjects will be randomized in a 4:1 ratio to receive a single dose of either SHR4640 (n=8) or placebo (n=2).

Registry
clinicaltrials.gov
Start Date
September 22, 2016
End Date
November 23, 2016
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male, aged between 18 and 55 years, inclusive.
  • Body weight ≥ 50 kg and body mass index between 18.0 to 30.0 kg/m2, inclusive.
  • Screening sUA level from 0.24 to 0.42 mmol/L, inclusive.
  • Considered generally healthy upon completion of medical history, full physical examination, vital signs, laboratory parameters (including thyroid function, coagulation and serological tests, hematology, creatinine kinase, biochemistry, and urinalysis), 12-lead ECG, and abdominal ultrasound, as judged by the Investigator.
  • Agrees to use a highly effective method of contraception, i.e. condom and suitable contraception for your female partner e.g. diaphragm (double barrier), oral contraceptive or intrauterine contraceptive device during heterosexual intercourse or be non-heterosexually active, or practice sexual abstinence throughout the study period and for 30 days following study drug dosing, and must agree to refrain from sperm donation from Day -2 until at least 30 days following study drug dosing.
  • Negative drug screen (including alcohol) at screening and on admission to clinical site.
  • Able to understand the study procedures and the risks involved and must be willing to provide written informed consent before any study-related activity.

Exclusion Criteria

  • History of hypersensitivity to SHR4640 or its analogues.
  • Screening sCr above upper limit of normal.
  • Screening alanine aminotransferase, aspartate aminotransferase, total bilirubin, or gamma glutamyl transferase \> 1.5 × upper limit of normal.
  • Positive result for HIV.
  • Positive result for hepatitis B surface antigen or hepatitis C virus antibody.
  • History or presence of kidney stones.
  • Acute or chronic illness that, in the opinion of the Investigator, might confound the results of the trial or pose risk in administering the trial product to the subject.
  • Undergone major surgery within 3 months of Day
  • Donated any blood or plasma in the past month or more than 400 mL within 3 months of Day
  • Has poor venous access and is unable to donate blood.

Arms & Interventions

2.5mg SHR4640

10 subjects will be randomized in a 4:1 ratio to receive a single dose of either 2.5 mg SHR4640 (n=8) or placebo (n=2)

Intervention: SHR4640

10mg SHR4640

10 subjects will be randomized in a 4:1 ratio to receive a single dose of either 10mg SHR4640 (n=8) or placebo (n=2) 10mg.

Intervention: SHR4640

20mg SHR4640

10 subjects will be randomized in a 4:1 ratio to receive a single dose of either 20mg SHR4640 (n=8) or placebo (n=2) .

Intervention: SHR4640

Placebo

For each dose cohort, 10 subjects will be randomized in a 4:1 ratio to receive a single dose of either SHR4640 (n=8) or placebo (n=2)

Intervention: Placebo

5mg SHR4640

10 subjects will be randomized in a 4:1 ratio to receive a single dose of either 5 mg SHR4640 (n=8) or placebo (n=2)

Intervention: SHR4640

Outcomes

Primary Outcomes

Assess safety and tolerability of SHR 4640 over 11days including AEs, laboratory safety variables (including hematology, creatinine kinase (CK), biochemistry, and urinalysis), physical examinations, vital signs, and 12-lead electrocardiograms (ECGs)

Time Frame: 11 days

Secondary Outcomes

  • Assess Pharmacokinetics (PK) Plasma parameter Area under the concentration-time curve (AUC) from zero to 24 and 72 hours postdose and from zero to infinity.(from time of dosing to 72 hours)
  • Assess Pharmacokinetics (PK) Plasma parameter Time to maximum concentration.(from time of dosing to 72 hours)
  • Assess Pharmacokinetics (PK) Plasma parameter Maximum concentration.(from time of dosing to 72 hours)
  • Assess Pharmacokinetics (PK) Plasma parameter Terminal elimination half-life (T1/2).(from time of dosing to 72 hours)
  • Assess Pharmacodynamics (PD) parameter Actual and percent changes in serum uric acid (sUA )from baseline.(from time of dosing to 72 hours)
  • Assess Pharmacodynamics (PD) parameter urinary uric acid concentration (uUA): actual and percent changes from baseline.(from time of dosing to 72 hours)
  • Assess Pharmacodynamics (PD) parameter urinary uric acid excretion (eUA): actual and percent changes from baseline.(from time of dosing to 72 hours)
  • Assess Pharmacodynamics (PD) parameter Uric acid renal clearance (UaCl): actual and percent changes from baseline(from time of dosing to 72 hours)

Study Sites (1)

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