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NCT00354198

Clinical Efficacy of Combined Pentoxifylline and Conventional Immunosuppressive Regimens on Patients With Rapidly Progressive Glomerulonephritis

Terminated Phase 3 Last updated 12 November 2012
What this trial tests

Phase 3 trial testing pentoxifylline in Glomerulonephritis in 7 participants. Terminated before completion.

Timeline
1 August 2006
Primary endpoint
1 August 2009
1 June 2010

Quick facts

Lead sponsorNational Taiwan University Hospital
PhasePhase 3
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment7
Start date1 August 2006
Primary completion1 August 2009
Estimated completion1 June 2010
Sites1 location across Taiwan

Drugs / interventions tested

Conditions studied

Sponsor

National Taiwan University Hospital

Who can join

Adults 20 to 80, any sex, with Glomerulonephritis. Healthy volunteers can join.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

We have recently demonstrated that pentoxifylline (PTX) has the potential to treat severe glomerular inflammation in a rat model of accelerated anti-glomerular basement membrane (GBM) glomerulonephritis. This study aims to investigate the therapeutic effects of combined PTX and conventional immunosuppressive regimens on patients with rapidly progressive glomerulonephritis.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of pentoxifylline

Trials testing the same drug.

Other recruiting trials for Glomerulonephritis

Currently open trials in the same condition.

Other National Taiwan University Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00354198.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing