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TRK-100STP PhaseII Clinical Study -Chronic Renal Failure (Primary Glomerular Disease/Nephrosclerosis)

Primary Purpose

Renal Insufficiency, Chronic

Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Beraprost
Placebo
Sponsored by
Toray Industries, Inc
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Renal Insufficiency, Chronic focused on measuring Chronic Renal Failure, Prostaglandin, Prostacyclin, Glomerular Disease; Nephrosclerosis

Eligibility Criteria

20 Years - 79 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • The CRF patient with primary glomerular disease or nephrosclerosis as the primary disease
  • The patient with progressive CRF

Exclusion Criteria:

  • The patient with secondary glomerular disease
  • The patient with CRF caused by pyelonephritis, interstitial/tubular nephritis, gouty kidney, polycystic kidney disease, or nephroureterolithiasis

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Experimental

    Experimental

    Placebo Comparator

    Arm Label

    1: Exprimental (TRK-100STP)

    2: Exprimental (TRK-100STP)

    3: Placebo Comparator

    Arm Description

    high dose

    low dose

    Placebo

    Outcomes

    Primary Outcome Measures

    Difference between the run-in and treatment periods in the slope of the regression line of 1/SCr versus time

    Secondary Outcome Measures

    Full Information

    First Posted
    June 21, 2015
    Last Updated
    June 26, 2015
    Sponsor
    Toray Industries, Inc
    Collaborators
    Astellas Pharma Inc
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02480751
    Brief Title
    TRK-100STP PhaseII Clinical Study -Chronic Renal Failure (Primary Glomerular Disease/Nephrosclerosis)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2015
    Overall Recruitment Status
    Completed
    Study Start Date
    October 2005 (undefined)
    Primary Completion Date
    May 2008 (Actual)
    Study Completion Date
    undefined (undefined)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Toray Industries, Inc
    Collaborators
    Astellas Pharma Inc

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The purpose of this study is to determine the recommended dose of the sustained-release form of BPS (TRK-100STP low dose or high dose) in Japanese patients with CRF (Primary glomerular disease/nephrosclerosis).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Renal Insufficiency, Chronic
    Keywords
    Chronic Renal Failure, Prostaglandin, Prostacyclin, Glomerular Disease; Nephrosclerosis

    7. Study Design

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

    8. Arms, Groups, and Interventions

    Arm Title
    1: Exprimental (TRK-100STP)
    Arm Type
    Experimental
    Arm Description
    high dose
    Arm Title
    2: Exprimental (TRK-100STP)
    Arm Type
    Experimental
    Arm Description
    low dose
    Arm Title
    3: Placebo Comparator
    Arm Type
    Placebo Comparator
    Arm Description
    Placebo
    Intervention Type
    Drug
    Intervention Name(s)
    Beraprost
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo
    Primary Outcome Measure Information:
    Title
    Difference between the run-in and treatment periods in the slope of the regression line of 1/SCr versus time
    Time Frame
    50 weeks (Run-in 22weeks, Treatment 28 weeks)

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    20 Years
    Maximum Age & Unit of Time
    79 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: The CRF patient with primary glomerular disease or nephrosclerosis as the primary disease The patient with progressive CRF Exclusion Criteria: The patient with secondary glomerular disease The patient with CRF caused by pyelonephritis, interstitial/tubular nephritis, gouty kidney, polycystic kidney disease, or nephroureterolithiasis

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    26475266
    Citation
    Koyama A, Fujita T, Gejyo F, Origasa H, Isono M, Kurumatani H, Okada K, Kanoh H, Kiriyama T, Yamada S. Orally active prostacyclin analogue beraprost sodium in patients with chronic kidney disease: a randomized, double-blind, placebo-controlled, phase II dose finding trial. BMC Nephrol. 2015 Oct 16;16:165. doi: 10.1186/s12882-015-0130-5.
    Results Reference
    derived

    Learn more about this trial

    TRK-100STP PhaseII Clinical Study -Chronic Renal Failure (Primary Glomerular Disease/Nephrosclerosis)

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