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D-0120 Safety and PK/PD Study in China

Primary Purpose

Hyperuricemia or Gout

Status
Completed
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
D-0120
Sponsored by
InventisBio Co., Ltd
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hyperuricemia or Gout

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Age ≥ 18 years old and ≤ 65 years old;
  2. Phase Ib: fasting sUA in the morning of screening period (fasted after 8:00 pm on the previous day) of healthy subjects meets the following requirement: 270 umol/l (4.5 mg/dL) ≤ sUA <420 umol/l (7 mg/dL)

    Phase IIa: hyperuricemia subjects should meet any of the following:

  3. Subject's BMI range is 18.0~32.0 kg/m2 (inclusive);
  4. Female subjects must be non-pregnant and non-lactating, surgically sterilized or ≥ 60 years old. Male subjects must be surgically sterilized or agree to practice sexual abstinence;
  5. Results of routine blood tests, blood biochemical tests and routine urine tests are within the normal range or clinically insignificant as judged by the principle investigator. Routine urine tests include normal urine creatinine, urine protein/creatinine ratio. ECGs are within the normal range or clinically insignificant as judged by the principle investigator.
  6. Subjects have the ability to follow study and follow-up procedures.
  7. Subjects have the ability to understand the study protocol and the risks involved, and must provide signed informed consent form to participate in the study.

Exclusion Criteria:

  1. History of significant metabolic, hematological, pulmonary, cardiovascular, gastrointestinal, nervous, hepatic, renal, urinary, gastrointestinal, immune, endocrine, psychiatric diseases, or clinical abnormalities that may pose excessive risks to the subjects or affect outcome or study interpretation at the discretion of the investigators;
  2. Allergic constitution, or allergy to any drug used in the study or any ingredient of study drug;
  3. History of malignant tumors;
  4. Subjects with positive results of any of the following items: screening hepatitis C antibody (HCV-Ab), human immunodeficiency virus antibody (HIV-Ab), hepatitis B surface antigen (HBsAg) and treponema pallidum (only for phase Ib healthy subjects);
  5. Urinary calculi confirmed by B-ultrasound during screening period;
  6. Myocardial infarction, angina pectoris, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, cerebral infarction, cerebral hemorrhage, subarachnoid hemorrhage or transient ischemic attack within 3 months prior to screening;
  7. Participation in clinical studies of any investigational drugs or medical devices within 3 months prior to screening;
  8. Major surgery within 3 months prior to randomization;
  9. Any clinically significant acute diseases within one month prior to screening at the discretion of the investigators;
  10. Gout flare within 14 days prior to randomization;
  11. Use of other uric acid-lowering drugs (allopurinol, febuxostat, probenecid, benzbromarone) within 14 days prior to randomization;
  12. Daily dose of aspirin > 100 mg within 14 days before randomization;
  13. Use of any diuretic within 14 days before randomization;
  14. Use of any Chinese herbal medicine within 14 days before randomization;
  15. History of drug abuse or alcohol abuse (for phase Ib healthy subjects, the screening alcohol test and urine drug test are positive);
  16. Any situation that may prevent the subject from completing the study or pose a significant risk to the subject as considered by any investigator;
  17. Any other situation that may pose excessive risks to the subject or affect outcome or study interpretation as considered by any investigator;

Sites / Locations

  • Site 04
  • Site 03
  • Site 07
  • Site 01- The second affiliated hospital of zhejiang university school of medicine
  • Site 06
  • Site 05

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

dose escalation in healthy subjects

dose escalation in hyperuricemia patients

Arm Description

Outcomes

Primary Outcome Measures

The number of subjects with treatment-related adverse events as assessed
Data will include clinical observations, ECG parameters, clinical chemistry and haematology and vital signs assessed as the number of subjects with treatment-related adverse events assessed

Secondary Outcome Measures

Time to observed Cmax (Tmax) for D-0120
Blood samples will be collected to assess plasma concentrations of D-0120 at a series of timepoints to derive Tmax
Area under the plasma concentration-time curve (AUC) for D-0120
Blood samples will be collected to assess plasma concentrations of D-0120 at a series of timepoints to derive AUC
Maximum Observed Plasma Concentration (Cmax) of D-0120
Blood samples will be collected to assess plasma concentrations of D-0120 at a series of timepoints to derive Cmax

Full Information

First Posted
April 18, 2019
Last Updated
May 5, 2022
Sponsor
InventisBio Co., Ltd
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1. Study Identification

Unique Protocol Identification Number
NCT03923868
Brief Title
D-0120 Safety and PK/PD Study in China
Official Title
A Randomized, Double-blind, Placebo-controlled, Multiple-administration, Multiple-dose, Phase Ib/IIa Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of D-0120 Tablets in Healthy Subjects and Hyperuricemia Patients in China
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Completed
Study Start Date
April 18, 2019 (Actual)
Primary Completion Date
December 31, 2021 (Actual)
Study Completion Date
December 31, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
InventisBio Co., Ltd

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hyperuricemia or Gout

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Sequential Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
52 (Actual)

8. Arms, Groups, and Interventions

Arm Title
dose escalation in healthy subjects
Arm Type
Experimental
Arm Title
dose escalation in hyperuricemia patients
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
D-0120
Intervention Description
D-0120 monotherapy dose escalation, oral, multiple dose for up to 28 days
Primary Outcome Measure Information:
Title
The number of subjects with treatment-related adverse events as assessed
Description
Data will include clinical observations, ECG parameters, clinical chemistry and haematology and vital signs assessed as the number of subjects with treatment-related adverse events assessed
Time Frame
Day 1 - Day 28
Secondary Outcome Measure Information:
Title
Time to observed Cmax (Tmax) for D-0120
Description
Blood samples will be collected to assess plasma concentrations of D-0120 at a series of timepoints to derive Tmax
Time Frame
Day 1 - Day 28
Title
Area under the plasma concentration-time curve (AUC) for D-0120
Description
Blood samples will be collected to assess plasma concentrations of D-0120 at a series of timepoints to derive AUC
Time Frame
Day 1 - Day 28
Title
Maximum Observed Plasma Concentration (Cmax) of D-0120
Description
Blood samples will be collected to assess plasma concentrations of D-0120 at a series of timepoints to derive Cmax
Time Frame
Day 1 - Day 28

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years old and ≤ 65 years old; Phase Ib: fasting sUA in the morning of screening period (fasted after 8:00 pm on the previous day) of healthy subjects meets the following requirement: 270 umol/l (4.5 mg/dL) ≤ sUA <420 umol/l (7 mg/dL) Phase IIa: hyperuricemia subjects should meet any of the following: Subject's BMI range is 18.0~32.0 kg/m2 (inclusive); Female subjects must be non-pregnant and non-lactating, surgically sterilized or ≥ 60 years old. Male subjects must be surgically sterilized or agree to practice sexual abstinence; Results of routine blood tests, blood biochemical tests and routine urine tests are within the normal range or clinically insignificant as judged by the principle investigator. Routine urine tests include normal urine creatinine, urine protein/creatinine ratio. ECGs are within the normal range or clinically insignificant as judged by the principle investigator. Subjects have the ability to follow study and follow-up procedures. Subjects have the ability to understand the study protocol and the risks involved, and must provide signed informed consent form to participate in the study. Exclusion Criteria: History of significant metabolic, hematological, pulmonary, cardiovascular, gastrointestinal, nervous, hepatic, renal, urinary, gastrointestinal, immune, endocrine, psychiatric diseases, or clinical abnormalities that may pose excessive risks to the subjects or affect outcome or study interpretation at the discretion of the investigators; Allergic constitution, or allergy to any drug used in the study or any ingredient of study drug; History of malignant tumors; Subjects with positive results of any of the following items: screening hepatitis C antibody (HCV-Ab), human immunodeficiency virus antibody (HIV-Ab), hepatitis B surface antigen (HBsAg) and treponema pallidum (only for phase Ib healthy subjects); Urinary calculi confirmed by B-ultrasound during screening period; Myocardial infarction, angina pectoris, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, cerebral infarction, cerebral hemorrhage, subarachnoid hemorrhage or transient ischemic attack within 3 months prior to screening; Participation in clinical studies of any investigational drugs or medical devices within 3 months prior to screening; Major surgery within 3 months prior to randomization; Any clinically significant acute diseases within one month prior to screening at the discretion of the investigators; Gout flare within 14 days prior to randomization; Use of other uric acid-lowering drugs (allopurinol, febuxostat, probenecid, benzbromarone) within 14 days prior to randomization; Daily dose of aspirin > 100 mg within 14 days before randomization; Use of any diuretic within 14 days before randomization; Use of any Chinese herbal medicine within 14 days before randomization; History of drug abuse or alcohol abuse (for phase Ib healthy subjects, the screening alcohol test and urine drug test are positive); Any situation that may prevent the subject from completing the study or pose a significant risk to the subject as considered by any investigator; Any other situation that may pose excessive risks to the subject or affect outcome or study interpretation as considered by any investigator;
Facility Information:
Facility Name
Site 04
City
Bengbu
State/Province
Anhui
Country
China
Facility Name
Site 03
City
Nanjing
State/Province
Jiangsu
Country
China
Facility Name
Site 07
City
Nanjing
State/Province
Jiangsu
Country
China
Facility Name
Site 01- The second affiliated hospital of zhejiang university school of medicine
City
Hangzhou
State/Province
Zhejiang
Country
China
Facility Name
Site 06
City
Huzhou
State/Province
Zhejiang
Country
China
Facility Name
Site 05
City
Wenzhou
State/Province
Zhejiang
Country
China

12. IPD Sharing Statement

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D-0120 Safety and PK/PD Study in China

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