Effect of Short Term Aliskiren Treatment in Kidney Transplant Patients

Mass General Brigham

Status and phase

Terminated

Phase 4

Conditions

Kidney Failure, Chronic

Kidney Disease

Treatments

Drug: Aliskiren

Drug: Placebo

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT01437943

2010P000005

Details and patient eligibility

About

The purpose of this study is to evaluate the effect of a short-term aliskiren treatment on kidney metabolism in patients at high risk for developing kidney dysfunction (i.e. kidney transplanted patients). The study is aimed at evaluating if any effect on kidney metabolism [using proton MR Spectroscopy(1H-MRS)] can be detected following a 6 months treatment with aliskiren regardless of its anti-hypertensive role. 1H-MRS can record a larger number of chemical species (up to 40) in the kidney, and monitor changes according to the pathologic state and health of the transplanted kidney.

Enrollment

10 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Stable patients with end stage renal disease receiving cadaveric kidney transplantation will be enrolled. Patients must have at least 6 months of follow-up to be included in the study. Patients must have stable creatinine levels in the last 6 months (no change>0.5 mg/dl).
Patients with a systolic blood pressure of 120 or above

Exclusion criteria

Serum potassium > 5.0 mmol/L (at the visit directly preceding Randomization);
History of any cardiovascular event (stroke, TIA, MI, unstable angina, CABG, percutaneous coronary intervention, hospitalization due to HF) during the 3 months prior to Visit 1. If a patient experiences such an event between Visit 1 and randomization at Visit 3, he/she should be withdrawn from the screening phase. If suitable, the patient can be re-screened at a later stage;
Hypertension (at enrollment): any patient with msSBP ≥ 170 mmHg or msDBP ≥ 110 mmHg;
Congestive heart failure NYHA class III and IV;
Concomitant treatment with two (2) or more renin-angiotensin-aldosterone system blocking agents, e.g. ACEI, ARB or aldosterone-antagonist;
Unstable serum creatinine, no patients with creatinine >2.5 mg/dl will be enrolled;
Second (II) or third (III) degree heart block without a pacemaker;
Concurrent potentially life threatening arrhythmia or other uncontrolled arrhythmia;
Clinically significant valvular heart disease;
Known renal artery stenosis;
Any surgical or medical condition which might significantly alter the absorption, distribution, metabolism, or excretion of the study drugs including, but not limited to, any of the following: (i) History of major gastrointestinal tract surgery such as gastrectomy, gastroenterostomy, or bowel resection (patients with previous bariatric surgery > 6 months prior to Visit 1 are allowed to participate); (ii) Any history of pancreatic injury, pancreatitis or evidence of impaired pancreatic function/injury as indicated by abnormal lipase or amylase; (iii) Evidence of hepatic disease as determined by any one of the following: SGPT value exceeding 3 x Upper Limit of Normal (ULN) at Visit 1, a history of hepatic encephalopathy, a history of cirrhosis, esophageal varices, or a history of portocaval shunt.
History of malignancy other than basal cell skin cancer within the past five years.
Any concurrent life threatening condition with a life expectancy less than 2 years.
History or evidence of drug or alcohol abuse within the last 12 months.
Any surgical or medical condition, which in the opinion of the investigator, may place the patient at higher risk from his/her participation in the study, or is likely to prevent the patient from complying with the requirements of the study or completing the study.
History of hypersensitivity to any of the study drugs or to medications belonging to the same therapeutic class as the study drugs as well as known or suspected contraindications to the study drugs.
History of noncompliance to medical regimens or unwillingness to comply with the study protocol.
Use of other investigational drugs at the time of enrollment, or within 30 days or 5 half-lives of enrollment, whichever is longer
Any condition that in the opinion of the investigator would jeopardize the evaluation of efficacy or safety.
Persons directly involved in the execution of this protocol.
Pregnant or nursing (lactating) women
Women of Child-Bearing Potential (WOCBP) unless postmenopausal for at least one year, surgically sterile or using effective methods of contraception as defined by local Health Authorities.
Treatment with Cyclosporine.

Exclusion criteria include MR contraindications:

electrical implants such as cardiac pacemakers or perfusion pumps
ferromagnetic implants such as aneurysm clips, surgical clips, prostheses, artificial hearts, valves with steel parts, metal fragments, shrapnel, tattoos near the eye, or steel implants
ferromagnetic objects such as jewelry or metal clips in clothing
pregnant volunteers
pre-existing medical conditions including a likelihood of developing seizures or claustrophobic reactions
any greater than normal potential for cardiac arrest
subjects less than 18 years of age.