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OpenTrials
Completed

NCT Number: NCT02689778

Effect of Pirfenidone on Glomerular Filtration Rate and Albuminuria in Patients With Diabetic Nephropathy

It is estimated that approximately 30% of patients with diabetes develop diabetic nephropathy. Diabetic nephropathy is a multifactorial progressive disease that occurs through various mechanisms such as hyperglycemia, oxidative stress, inflammation and fibrosis, control or blocking these mechanisms are therefore potential therapeutical targets for this entity. Current treatment options are based on the glycemic control, blood pressure control, as well as the use of medications such as angiotensin-converting enzyme inhibitors and Angiotensin II receptor antagonists, these actions are not enough to stop progression. Pirfenidone is a drug with antifibrotic, antioxidant, and anti-inflammatory properties. Although the specific mechanism is unknown, pirfenidone interferes with the expression, secretion and the effect of the β (TGF-β) transforming growth factor. The investigators plan to carry out a controlled clinical study to evaluate the effect of pirfenidone in patients with type 2 diabetes and nephropathy. The period of time the treatment will be administered will be of 12 months, 62 patients will be included. The primary outcome will be improvement in glomerular filtration rate. The secondary outcomes will be number of patients requiring replacement therapy, 24 hour urine microalbuminuria and change in the concentration of TGF - β. Change in these parameters will be evaluated at the end of the treatment period (12 months). Throughout the study the incidence of adverse events will be recorded, wich will allow us to learn about the safety and security of the drug in this population.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Body mass index (BMI) less than 35 kg/m2
  • Diagnosis of diabetes mellitus type 2
  • Glomerular filtration rate of 15-89 ml/min
  • Albuminuria ≥30 mg/24 h and < 3.5 g/24 h
  • Individuals with blood pressure less than 140/90 mmHg or treated with stable doses of anti-hypertensive drugs.
  • Glycated hemoglobin <10%

Exclusion criteria

  • Another etiology of renal disease (autoimmune diseases, polycystic kidney disease)
  • Repeated urinary tract infections (more than three episodes in the past year)
  • Photosensitivity to any drug
  • Liver disease
  • Pregnancy
  • Breastfeeding

Treatment and study plan

pirfenidone

Drug

Oral pirfenidone 600 mg with breakfast and 1200 mg pirfenidone with dinner for 12 months.

Other names: Kitoscell LP

Placebo

Drug

Identical tablets without active substance

Primary outcomes

  1. Effect of oral pirfenidone (1800 mg) in albuminuria

    Time frame: 12 months

  2. Effect of oral pirfenidone (1800 mg) in glomerular filtration rate

    Time frame: 12 months

Secondary outcomes

  1. Number of patients with treatment related adverse events

    Time frame: 12 months

    hypersensitivity, photosensitivity, liver function test alteration

Sponsors and collaborators

Lead sponsor

Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran

Other

Collaborators

  • Grupo Medifarma, S. A. de C. V.

Registry information

Important dates

Study start
2016
Primary completion
2019
Study completion
2019
First posted
Feb 24, 2016
Registry last updated
Mar 14, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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