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Change From Baseline to Chronic Kidney Disease Patient Before and After Administration Drug

Primary Purpose

Chronic Renal Failure

Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Placebo
HD-003 (800mg/day)
HD-003 (1600mg/day)
Sponsored by
Hyundai Pharmaceutical Co., LTD.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Renal Failure focused on measuring in stage 3 or 4 steps

Eligibility Criteria

20 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patient diagnosed with chronic renal failure which subjected to conservation therapy.
  2. Patient has 15~59mL/min/1.736m2 glomerular filtration rate.
  3. Serum creatinine(sCr) is in the range of 1.5~5.0mg/dL at the start of the test and until the start of the test from 52 weeks the serum creatinine is three times more than the number of measurements, and during the final test values of serum creatinine patients with advanced value rises 0.2mg/dL or higher than the first tests.
  4. From the start of the test until 52 weeks before the test, serum creatinine the slope of the straight line for the inverse of the value is less than the rare patient -0.0001
  5. Inpatient or outpatient
  6. Age: 20~75, gender: both

Exclusion Criteria:

  1. Patient who start treatment drug or diet that maybe inhibit progress of renal failure within 3 months of the study start
  2. Diabetic patients with unstable blood sugar regulation.
  3. Patient did not have blood pressure control
  4. Patient taking the combination of prohibited substances
  5. Dialysis patient
  6. Patient with gout
  7. Patient who merged with a progressive muscular dystrophy, polymyositis, etc.
  8. Patients with symptoms of cerebral vascular disorders
  9. Women who are pregnant or breast-feeding
  10. Patient with infectious disease
  11. Patient with gastric ulcer
  12. Patients who has difficult diet, medication, etc.
  13. Patients with genetic problems such as galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption
  14. Subjects with decision of nonparticipation through investigator's review due to laboratory test results or other excuse such as non-responding to request or instruction by investigator

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Placebo Comparator

    Experimental

    Experimental

    Arm Label

    Placebo group

    HD-003 (800mg/day)

    HD-003 (1600mg/day)

    Arm Description

    Outcomes

    Primary Outcome Measures

    serum creatinine rate inverse number's change
    GFR measurements (confirmed by the method MDRD via the value of sCr)

    Secondary Outcome Measures

    Full Information

    First Posted
    February 10, 2015
    Last Updated
    June 15, 2017
    Sponsor
    Hyundai Pharmaceutical Co., LTD.
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02378194
    Brief Title
    Change From Baseline to Chronic Kidney Disease Patient Before and After Administration Drug
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2015
    Overall Recruitment Status
    Completed
    Study Start Date
    January 2010 (Actual)
    Primary Completion Date
    March 2013 (Actual)
    Study Completion Date
    March 2013 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Hyundai Pharmaceutical Co., LTD.

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Chronic renal failure is a syndrome that renal function is decreased, and the patient number is increasing. In addition, patients on dialysis have also increased. Depending on the chronic renal failure aggravated, the deterioration of life caused by the conduct of dialysis patients is caused. In addition, a problem in dialysis treatment is ongoing economic burden surface to increase the life of the patient and family. A solution to this problem is, or stops the progression of chronic renal failure prior to dialysis, it is necessary to delay. As a treatment for inhibiting the progression of chronic renal failure is present, along with diet and blood pressure-lowering drugs or a drug therapy used by kremezin. However, the effect is not enough, new drug development is required. HD-003 is a novel compound, and found to inhibit the renal failure progression. It was found during the search active substance that appear when the inflammation in animals. The investigators confirmed that the substance is present in the urine of a person during the study, and later established a link between kidney disease hypotheses. When performing the test in animal model renal failure, chronic renal Through the non-clinical testing of the HD-003(general toxicity studies, reproductive, developmental toxicity test, mutagenicity test and antigen tests) showed that a very low toxicity. When going through the review of the safety and pharmacokinetic Phase 1 clinical study, it was confirmed a very satisfactory safety and tolerability. And pharmacokinetic results from the body's absorption in healthy subjects had been done well, a linear correlation was observed. Finally, it was confirmed that the most rapidly excreted into the urine. This study is a Phase 2a clinical trials performed in patients with chronic renal failure in 3, 4 steps. The evaluation of changes in serum creatinine(sCr) in vivo indicator of renal failure according to the progress. Evaluating the inhibitory effect of HD-003 renal failure progression and dose setting, and to determine the safety.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Chronic Renal Failure
    Keywords
    in stage 3 or 4 steps

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    62 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Placebo group
    Arm Type
    Placebo Comparator
    Arm Title
    HD-003 (800mg/day)
    Arm Type
    Experimental
    Arm Title
    HD-003 (1600mg/day)
    Arm Type
    Experimental
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo
    Intervention Description
    24 weeks, once daily oral administration
    Intervention Type
    Drug
    Intervention Name(s)
    HD-003 (800mg/day)
    Intervention Description
    24 weeks, once daily oral administration
    Intervention Type
    Drug
    Intervention Name(s)
    HD-003 (1600mg/day)
    Intervention Description
    24 weeks, once daily oral administration
    Primary Outcome Measure Information:
    Title
    serum creatinine rate inverse number's change
    Time Frame
    up to 24 weeks
    Title
    GFR measurements (confirmed by the method MDRD via the value of sCr)
    Time Frame
    up to 24 weeks
    Other Pre-specified Outcome Measures:
    Title
    Number of Participants with Adverse Events
    Time Frame
    up to 1 year

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    20 Years
    Maximum Age & Unit of Time
    75 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patient diagnosed with chronic renal failure which subjected to conservation therapy. Patient has 15~59mL/min/1.736m2 glomerular filtration rate. Serum creatinine(sCr) is in the range of 1.5~5.0mg/dL at the start of the test and until the start of the test from 52 weeks the serum creatinine is three times more than the number of measurements, and during the final test values of serum creatinine patients with advanced value rises 0.2mg/dL or higher than the first tests. From the start of the test until 52 weeks before the test, serum creatinine the slope of the straight line for the inverse of the value is less than the rare patient -0.0001 Inpatient or outpatient Age: 20~75, gender: both Exclusion Criteria: Patient who start treatment drug or diet that maybe inhibit progress of renal failure within 3 months of the study start Diabetic patients with unstable blood sugar regulation. Patient did not have blood pressure control Patient taking the combination of prohibited substances Dialysis patient Patient with gout Patient who merged with a progressive muscular dystrophy, polymyositis, etc. Patients with symptoms of cerebral vascular disorders Women who are pregnant or breast-feeding Patient with infectious disease Patient with gastric ulcer Patients who has difficult diet, medication, etc. Patients with genetic problems such as galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption Subjects with decision of nonparticipation through investigator's review due to laboratory test results or other excuse such as non-responding to request or instruction by investigator
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Choi
    Organizational Affiliation
    Yonsei University Health System, Severance Hospital
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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