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Clinical trialNCT02156843TerminatedPhase 3Interventional

Pyridorin in Diabetic Nephropathy

SponsorNephroGenex, Inc.Enrollment328Diabetic Kidney DiseaseDiabetic Nephropathy
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of this study is to evaluate the safety and efficacy of oral Pyridorin 300 mg BID in reducing the rate of progression of nephropathy due to type 2 diabetes mellitus.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

137 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Australia
  • Csg Investigational Site (#205)

    Camperdown, New South Wales, Australia

  • Csg Investigational Site (#201)

    Gosford, New South Wales, Australia

  • Csg Investigational Site (#206)

    Liverpool, New South Wales, Australia

  • Csg Investigational Site (#208)

    St Leonards, New South Wales, Australia

  • Csg Investigative Site (#204)

    Adelaide, South Australia, Australia

  • Csg Investigational Site (#207)

    Footscray, Victoria, Australia

  • Csg Investigational Site (#200)

    Reservoir, Victoria, Australia

  • Csg Investigational Site (#202)

    Richmond, Victoria, Australia

  • Csg Investigational Site (#209)

    Parkville, Australia

Bulgaria
  • Csg Investigational Site (#757)

    Plovdiv, Bulgaria

  • Csg Investigational Site (# 750)

    Sofia, Bulgaria

  • Csg Investigational Site (# 755)

    Sofia, Bulgaria

  • Csg Investigational Site (# 756)

    Sofia, Bulgaria

  • Csg Investigational Site (#751)

    Sofia, Bulgaria

  • Csg Investigational Site (#752)

    Sofia, Bulgaria

  • Csg Investigational Site (#753)

    Sofia, Bulgaria

  • Csg Investigational Site (#754)

    Stara Zagora, Bulgaria

France
  • Csg Investigational Site (#801)

    Grenoble, Cedex, France

  • Csg Investigational Site (#802)

    Paris, Cedex, France

  • Csg Investigational Site (#800)

    Boulogne-sur-Mer, France

  • Csg Investigational Site (#803)

    Colmar, France

  • Csg Investigational Site (#806)

    Montpellier, France

  • Csg Investigational Site (#804)

    Rhone, France

  • Csg Investigational Site (#805)

    Valenciennes, France

Germany
  • Csg Investigational Site (#709)

    Aschaffenburg, Germany

  • Csg Investigative Site (#702)

    Berlin, Germany

  • Csg Investigational Site (#706)

    Elsterwerda, Germany

  • Csg Investigational Site (#703)

    Heidelberg, Germany

  • Csg Investigational Site (#707)

    Herzberg, Germany

  • Csg Investigational Site (#701)

    Hoyerswerda, Germany

  • Csg Investigational Site (#708)

    Mainz, Germany

  • Csg Investigational Site (#700)

    München, Germany

Hong Kong
  • Csg Investigational Site (#400)

    Hong Kong, Hong Kong

  • Csg Investigational Site (#402)

    Kwai Chung, Hong Kong

  • Csg Investigational Site (#401)

    Shatin, Hong Kong

Hungary
  • Csg Investigational Site (#501)

    Balatonfüred, Hungary

  • Csg Investigational Site (#505)

    Budapest, Hungary

  • Csg Investigational Site (#509)

    Budapest, Hungary

  • Csg Investigational Site (#513)

    Budapest, Hungary

  • Csg Investigational Site (#507)

    Debrecen, Hungary

97 more sites on the registry record.ClinicalTrials.gov ↗

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

PlaceboPyridorin
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
30 Jun 2014
Primary completion
31 Dec 2017
Completion
31 Mar 2018
Last update posted
9 Mar 2016
Registered enrollment
328
Registry id
NCT02156843

Cross-registrations

EU-CTR / CTIS (EudraCT)2014-001641-24

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.