Status:
COMPLETED
Direct Renin Inhibition and the Kidney
Lead Sponsor:
Vitae Pharmaceuticals, Inc.
Collaborating Sponsors:
Brigham and Women's Hospital
Conditions:
Renal Function
Eligibility:
All Genders
18-75 years
Phase:
PHASE1
Brief Summary
The objective of the study is to determine the magnitude of the effect of direct renin inhibition by VTP-27999 on renal plasma flow and kidney function.
Eligibility Criteria
Inclusion
- Healthy adult male or female, 18-75 years of age
- Female subjects must be postmenopausal or surgically sterilized. Postmenopausal females must have had no regular menstrual bleeding for at least one (1) year prior to initial dosing. Menopause will be confirmed by plasma serum FSH level at screening between 23.0-116.3 mIU/ml. Female subjects who report surgical sterilization must have had the procedure at least six (6) months prior to initial dosing.
- Male subjects, able to father a child, must be willing to use approved birth control methods for 2 weeks following completion of study.
Exclusion
- Subjects under 18 and subjects over 75 years
- Diabetes Mellitus and/or kidney disease
- Myocardial infarction, stroke, or cardiovascular revascularization/angioplasty within the last 6 months
- Unstable angina pectoris or CAD requiring treatment with an excluded concomitant medication
- History of/or symptoms consistent with congestive heart failure
- Hypertension
- History of left ventricular ejection fraction \< 45%
- Current smokers or nicotine patch
- Pregnant or lactating females
- Cancer or any life threatening illness with expected death within 2 years or by completion of the study
- Serum creatinine \>1.4 mg/dl
- Serum potassium \<3.5 or \>5.2 mmol/L without medication
- Serum albumin \< 2.0 g/dL
- Hemoglobin \< 11.5 g/dL or Hematocrit \< 34%
- Any serum AST \>/= 60 or ALT \>/= 75 IU/L
- Use of any prescription drugs which may affect the renin-angiotensin-aldosterone system or with known effect on renal hemodynamics are not allowed within 10 days prior to dosing or during the study
- Use of CYP3A4 inhibitors (e.g. Diltiazem, Ketoconazole, Nifedipine, or Verapamil)
- Use of any prescription medication is prohibited within 14 days (or, if known, for at least 5 half-lives, if longer) prior to dosing, unless approved by both the Investigator and the Sponsor
- Use of any over-the-counter (OTC) medication, including herbal products, is prohibited within the 14 days prior to dosing, unless approved by both the Investigator and the Sponsor
- Donation or loss of 400 mL or more of blood within 8 weeks prior to first dosing
- A known hypersensitivity or contraindication to the study drugs (Aliskiren) or drugs similar to the study drugs or PAH, and inulin
- Any surgical or medical condition which alters absorption, distribution, metabolism or excretion of drugs or which may jeopardize the patient subject during this study, including gastric bypass
- History of drug or alcohol abuse within the 12 months prior to dosing, or evidence of such abuse as indicated by past medical history
- Acute infections and/or significant illness within 3 weeks of planned enrollment into this study
- Any medical condition in the investigator's opinion, which renders the subject unable to complete the study or which would produce significant risk to the subject
- Administration of any other investigational drug within 30 days of planned dosing in the study
- Poor intravenous (IV) access as determined by the study staff
Key Trial Info
Start Date :
September 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 1 2011
Estimated Enrollment :
22 Patients enrolled
Trial Details
Trial ID
NCT01217736
Start Date
September 1 2010
End Date
November 1 2011
Last Update
February 29 2016
Active Locations (1)
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1
Brigham and Women's Hospital
Boston, Massachusetts, United States, 02115