Direct Renin Inhibition and the Kidney

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.

Study Overview

• Status: Completed
• Conditions: Renal Function
• Intervention / Treatment: Drug: VTP-27999; Drug: aliskiren; Drug: placebo

• Study Type: Interventional
• Enrollment (Actual): 22
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • Massachusetts
    • Boston, Massachusetts, United States, 02115
      • Brigham and Women's Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 75 years (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• 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 Criteria:

• 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

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Basic Science
• Allocation: Non-Randomized
• Interventional Model: Crossover Assignment
• Masking: None (Open Label)

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Placebo Comparator: placebo	Drug: placebo; single dose, tablet
Experimental: VTP-27999	Drug: VTP-27999; single dose, tablet
Active Comparator: aliskiren	Drug: aliskiren; single dose, tablet; Other Names: Tekturna

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
renal plasma flow	as measured by PAH clearance	pre-dose to 6 hours post-dose

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
glomerular filtration rate		pre-dose to 6 hours post-dose
RAAS pathway biomarkers	renin, prorenin, plasma renin activity, ang II	pre-dose to 24 hours post-dose
VTP-27999 concentrations		pre-dose to 24 hours post-dose

Collaborators and Investigators

• Sponsor: Vitae Pharmaceuticals, Inc.
• Collaborators: Brigham and Women's Hospital
• Investigators: Principal Investigator: Norman K Hollenberg, MD, PhD, Brigham and Women's Hospital, Boston, MA

Publications and helpful links

General Publications

• Barkoudah E, Danser AHJ, van Thiel BS, Fisher NDL, Gregg R, Hollenberg NK. Journal of the American Society of Hypertension 9(4)
• Barkoudah E, van Thiel BS, Fisher ND, Gregg RA, Danser AH, Moukarbel GV, Hollenberg NK. Maximum renal responses to renin inhibition in healthy study participants: VTP-27999 versus aliskiren. J Hypertens. 2016 May;34(5):935-41. doi: 10.1097/HJH.0000000000000860.

Helpful Links

• maximum renal responses in healthy study participants: VTP-27999 versus aliskiren

Study record dates

Study Major Dates

• Study Start: September 1, 2010
• Primary Completion (Actual): November 1, 2011
• Study Completion (Actual): November 1, 2011

Study Registration Dates

• First Submitted: October 6, 2010
• First Submitted That Met QC Criteria: October 6, 2010
• First Posted (Estimate): October 8, 2010

Study Record Updates

• Last Update Posted (Estimate): February 29, 2016
• Last Update Submitted That Met QC Criteria: February 26, 2016
• Last Verified: February 1, 2016

More Information

Terms related to this study

• Other Study ID Numbers: VTP-27999-005; 2010P001281 (Other Identifier: Partners Healthcare System)