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
About this trial
This is an interventional treatment trial for Chronic Renal Failure focused on measuring in stage 3 or 4 steps
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
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
NCT ID
NCT02378194
First Posted
February 10, 2015
Last Updated
June 15, 2017
Sponsor
Hyundai Pharmaceutical Co., LTD.
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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Change From Baseline to Chronic Kidney Disease Patient Before and After Administration Drug
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