Sitaxsentan in Proteinuric Chronic Kidney Disease

Chronic Kidney Disease Clinical Trial

Official title:

The Effect of Sitaxsentan Once Daily Dosing on Proteinuria, 24-Hour Systemic Blood Pressure, and Arterial Stiffness in Subjects With Chronic Kidney Disease

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT00817037
• Other study ID #: 2007/W/CRC/02
• Secondary ID: CTA# 2006-002004
• Status: Active, not recruiting
• Phase: Phase 2
• First received: January 5, 2009
• Last updated: January 5, 2009
• Start date: May 2007

Study information

• Verified date: January 2009
• Source: University of Edinburgh
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: Medicines and Healthcare Products Regulatory Agency
• Study type: Interventional

Clinical Trial Summary

Patients with chronic kidney disease (CKD) have higher blood pressures than the general population. They also tend to have protein leaking into the urine (proteinuria). CKD, high blood pressure and proteinuria independently and together increase the risk of developing atherosclerosis (hardening) of the arteries that leads to diseases such as heart attack and stroke. Although there are a number of drugs available that lower blood pressure, these are not always fully effective. Furthermore, there are even fewer drugs that simultaneously lower blood pressure, reduce proteinuria, and slow down kidney damage in CKD.

Recent research has shown that drugs like sitaxsentan not only lower blood pressure but also reduce proteinuria and potentially slow down the progression of CKD [1,2]. Before sitaxsentan can become freely available to individuals with CKD it is important to look at the effects this drug could have on proteinuria and blood pressure.

1. Goddard J, Johnston NR, Hand MF, et al. Endothelin-A receptor antagonism reduces blood pressure and increases renal blood flow in hypertensive patients with chronic renal failure: a comparison of selective and combined endothelin receptor blockade. Circulation 2004;109:1186-1193.

2. Krum H, Viskoper RJ, Lacourciere Y et al. The effect of an endothelin receptor antagonist, bosentan, on blood pressure in patients with essential hypertension. New Engl J Med 1998;338:784-790.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 27
• Est. primary completion date: March 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

1. Has Stage 1-5 chronic kidney disease (CKD) as defined by the Kidney Disease Outcomes Quality Initiative (using the Cockcroft and Gault equation for calculation of glomerular filtration rate) with proteinuria, including any of the following aetiologies: immunoglobulin A (IgA) nephropathy, polycystic kidney disease (PCKD), congenital abnormalities, reflux nephropathy, focal segmental glomerulosclerosis, minimal change nephropathy, and membranous nephropathy.

2. Is between 18 and 70 years of age, inclusive.

3. Has a body mass index (BMI) between 18 and 35 kg/m2, inclusive.

4. Is willing and able to adhere to the protocol requirements.

5. Provides written informed consent before any study procedure is performed.

Exclusion Criteria:

1. Requires peritoneal dialysis or haemodialysis.

2. Has kidney disease due to diabetes mellitus, vasculitis, systemic lupus erythematosus, or known renovascular disease; antiglomerular basement membrane disease; or is on immunosuppressive medication.

3. Has a serum albumin in the nephrotic range (< 30 g/L) during Screening.

4. Has a sustained sitting systolic blood pressure (BP) > 160 mmHg or sustained sitting diastolic BP > 100 mmHg during Screening.

5. Has postural hypotension during Screening, which is defined as a decrease in systolic BP = 20 mmHg and/or a decrease in diastolic BP = 10 mmHg, comparing sitting and standing measurements.

6. Has a history and/or evidence of ischaemic heart disease.

7. Has or had a malignancy, with the exception of adequately-treated basal cell or squamous cell carcinoma of the skin, that required significant medical intervention within the past 3 months and/or is likely to result in death within the next 2 years.

8. Has a history of allergies or hypersensitivity to sitaxsentan or nifedipine or the excipients of either drug.

9. Has a clinically significant psychiatric, addictive, neurological disease or any other condition that, in the Investigator's opinion, would compromise his/her ability to give informed consent, participate fully in this study, prevent adherence to the requirements of the study protocol, or would compromise the interpretation of the data obtained from this study.

10. Uses a prohibited medication or plans to use a prohibited medication during the study.

• Prohibited medications include cyclosporine A, alternative endothelin (ET) receptor antagonists, phosphodiesterase inhibitors, and/or vitamin K antagonists (e.g., warfarin). The intermittent use of phosphodiesterase inhibitors (e.g., sildenafil) "as needed" for erectile dysfunction is acceptable, however, as long as the subject is not dosed within 24 hours of an efficacy assessment.

11. Received treatment with an investigational drug or device within 30 days prior to study entry.

12. Has a history of organ transplantation.

13. Has atrial fibrillation requiring anticoagulation or a history (in the preceding 6 months) of any intermittent cardiac dysrhythmia that may require anticoagulation therapy.

14. Has an alanine aminotransferase (ALT) and/or aspartate aminotransferase (AST) level > 1.5 × the upper limit of the normal range (ULN) at Screening and/or serum total bilirubin > ULN.

15. Has a haemoglobin concentration < 8.0 mg/dL at Screening.

16. Has positive serological results for hepatitis B and/or hepatitis C.

17. Is a woman of childbearing potential who is unwilling to use 2 forms of contraceptive therapy, including at least 1 barrier method, throughout the study. (Women who are surgically sterile or who are post-menopausal for at least 2 years are not considered to be of childbearing potential.)

18. Is pregnant, lactating, or breastfeeding.

19. Has, in the opinion of the Investigator, a dependence on alcohol.

20. Has, in the opinion of the Investigator, a dependence on illicit drugs.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Blood Pressure
• Chronic Kidney Disease
• Kidney Diseases
• Proteinuria
• Renal Insufficiency, Chronic

Intervention

Drug:
• Sitaxsentan
Sitaxsentan 100mg once daily oral dosing for 6 weeks
• Nifedipine
Nifedipine 30mg once daily oral dosing for 6 weeks
• Placebo tablet
Placebo tablet once daily oral dosing for 6 weeks

Locations

Country	Name	City	State
United Kingdom	Clinical Research Centre, Western General Hospital	Edinburgh	Scotland

Sponsors (2)

Lead Sponsor	Collaborator
University of Edinburgh	Encysive Pharmaceuticals

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The principal objective of this study is to evaluate whether sitaxsentan reduces proteinuria in people with chronic kidney disease.		6 Weeks	No
Secondary	Secondary objective of this study is to evaluate whether sitaxsentan reduces systemic blood pressure in people with chronic kidney disease.		6 weeks	No
Secondary	Secondary objective is to determine whether sitaxsentan improves indices of arterial stiffness in people with chronic kidney disease		6 weeks	No
Secondary	Secondary objectives is to determine the safety of sitaxsentan in chronic kidney disease		6 weeks	Yes