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A phase II study for treatment of proteinuria in patients currently on irbesartan therapy

Phase 2
Completed
Conditions
Proteinuria
Renal and Urogenital - Kidney disease
Registration Number
ACTRN12614001132639
Lead Sponsor
Dimerix Bioscience Pty Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
27
Inclusion Criteria

Capable of providing informed consent.
Women of child bearing potential or men of reproductive potential must be using adequate birth control measures.
Previously diagnosed with protein in the urine and have a protein/creatinine ratio (PCR) of greater than 50 (mg/mmol) based on 24 hour urine collection.
Patients with a defined level of kidney function as follows:
- serum creatinine 115 to 291 micromol/L inclusive for women
- serum creatinine 132 to 309 micromol/L inclusive for men
- or estimated GFR 20-60
Taking stable irbesartan with BP in range of 110/70 to 150/95 mmHg. (Stable is defined as taking the same dose of IRB for at least 90 days prior to baseline).
Liver function tests less than or equal to 2X upper limit of normal
Patients taking a diuretic must be on a stable dose for at least 2 months.

Exclusion Criteria

Rapidly progressing proteinuria (rapidly progressing is defined as a trebling of proteinuria over the preceding 3 month period)
Recent gastrointestinal bleeding
Heart disease that is not considered stable
Acute kidney injury within the 3 months before screening
Are receiving any ACE inhibitor, NSAID therapy or spironolactone
Have uncontrolled blood pressure
Required to take drugs that change the immune system (immunosupressants)
HIV infection
Viral Hepatitis B or C, liver infection, liver cirrhosis or any clinically significant liver damage. (Liver function tests > 2X ULN)
Cancer within 3 years (excluding non melanoma skin cancer) or high risk of developing cancer
Major surgery within 3 months of screening or planned during the study period.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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