“SALT Trial” Study of Ascending Levels of Tolvaptan in Hyponatremia

This study has been completed.
Sponsor:
Collaborator:
Otsuka Pharmaceutical Co., Ltd.
Information provided by:
Otsuka Pharmaceutical Development & Commercialization, Inc.
ClinicalTrials.gov Identifier:
NCT00072683
First received: November 7, 2003
Last updated: January 24, 2007
Last verified: January 2007
  Purpose

This study’s purpose is to determine whether tolvaptan can safely and effectively return the body’s balance of sodium and water toward normal, and to characterize and quantify the potential clinical benefits of this treatment.


Condition Intervention Phase
Hyponatremias
Water Intoxication
Inappropriate ADH Syndrome
Water-Electrolyte Imbalances
Drug: tolvaptan
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double-Blind
Primary Purpose: Treatment
Official Title: Multicenter, Randomized, Double-Blind, Placebo-Controlled, Efficacy and Safety Study of the Effects of Titrated Oral Tolvaptan Tablets in Patients With Hyponatremia

Resource links provided by NLM:


Further study details as provided by Otsuka Pharmaceutical Development & Commercialization, Inc.:

Primary Outcome Measures:
  • The average daily area under the curve of change from baseline in serum sodium level up to Day 4 within the double-blind on therapy period. and/or
  • The average daily area under the curve of change from baseline in serum sodium level up to Day 30 within

Secondary Outcome Measures:
  • The average daily area under the curve of change from baseline in serum sodium level up to Day 4 within the double-blind on therapy period for patients with severe hyponatremia (serum sodium <130 mEq/L at baseline).
  • The average daily area under the curve of change from baseline in serum sodium level up to Day 30 within the double-blind on therapy period for patients with severe hyponatremia (serum sodium <130 mEq/L at baseline).
  • Percentage of patients with normalized serum sodium at Day 4.
  • Percentage of patients with normalized serum sodium at Day 30.
  • Time to first normalization in serum sodium.
  • Change from baseline in serum sodium at Day 4.
  • Change from baseline in serum sodium at Day 30.
  • Percentage of patients requiring fluid restriction at any time during the double-blind on therapy period of the study.
  • Urine output at Day 1.
  • Change from baseline in body weight at Day 1 (hypervolemic patients only).
  • Fluid balance at Day 1 (hypervolemic patients only).
  • Change from baseline in the SF-12 (health survey)Physical Component Summary (PCS)and Mental Component Summary (MCS)scales at Week 1 and Day 30.
  • Categorical change in serum sodium at Day 4 and Day 30 for patients with baseline serum sodium <130 mEq/L.
  • Categorical change in serum sodium at Day 4 and Day 30 for patients with baseline serum sodium ≥130 mEq/L.
  • The percentage of patients who are designated as treatment failure due to the need for saline infusion,with or without fluid restriction.
  • Safety:Adverse events,vital signs,clinical laboratory tests,12- lead electrocardiograms.
  • PK:Plasma tolvaptan and DM-4103 concentrations.

Estimated Enrollment: 240
Study Start Date: April 2003
Estimated Study Completion Date: February 2006
Detailed Description:

Hyponatremia is defined as a serum sodium concentration below the lower limit of normal and is the most frequently encountered electrolyte abnormality in hospitalized patients. Generally speaking, most cases of hyponatremia are mild. However, as the serum sodium falls below 130 mEq/L, the possibility of significant morbidity and mortality increases, and most clinicians will initiate corrective therapy for serum sodium values approaching 130 mEq/L and lower. The reasons for treating hyponatremia relate both to the symptoms, which may be quite disturbing to patients, as well as to potential outcomes including permanent neurological damage and death. There is also growing awareness of the association between hyponatremia and increased mortality in patients with heart failure.A common theme underlying the occurrence of hyponatremia whether in the setting of congestive heart failure, hepatic failure with ascites, or the syndrome of inappropriate anti-diuretic hormone (SIADH) is the non-osmotic secretion of arginine vasopressin (AVP). The presence of excess AVP leads to fluid retention and hyponatremia. Agents that antagonize AVP, causing proportionally more water diuresis than solute excretion, could offer a significant treatment option for patients with hyponatremia, compared to fluid restriction alone. Treatment of hyponatremia, particularly in clinical settings such as decompensated congestive heart failure, is difficult as conventional diuretics cause neurohormonal activation and further stimulate the inappropriate release of vasopressin, leading to additional retention of free water and aggravation of hypoosmolality. Similarly, for cirrhosis with ascites and SIADH, conventional diuretics are either minimally effective or completely contraindicated. An alternative approach to symptom relief and treatment of hyponatremia may be the use of vasopressin antagonists, which increase free water clearance with proportionally less effect on sodium excretion. Tolvaptan is an oral vasopressin antagonist with relative affinity for the V2 receptor which has been shown to induce a diuresis with proportionally more free-water than sodium loss. The current study is being undertaken in order to evaluate whether tolvaptan, an oral AVP inhibitor, will be effective in correcting mild to moderate hyponatremia, and to elucidate the effect of this correction on the subject’s well-being.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria

  • Hyponatremia in euvolemic or hypervolemic states, defined as serum sodium <135 mEq/L prior to randomization.
  • Able to give Informed Consent

Exclusion Criteria

  • Women who are breast feeding and females of childbearing potential who are not using acceptable contraceptive methods
  • Hyponatremia in hypovolemic states.
  • Acute and transient hyponatremia associated with head trauma or post-operative state.
  • Hyponatremia due to uncontrolled hypothyroidism or uncontrolled adrenal insufficiency.
  • Cardiac surgery within 30 days of potential study enrollment, excluding percutaneous coronary interventions.
  • History of a myocardial infarction within 30 days of potential study enrollment.
  • History of sustained ventricular tachycardia or ventricular fibrillation within 30 days, unless in the presence of an automatic implantable cardioverter defibrillator.
  • Severe angina including angina at rest or at slight exertion and/or unstable angina.
  • History of a cerebrovascular accident within the last 30 days. 10) Subjects with psychogenic polydipsia may not be included, however subjects with other psychiatric illness may be included.
  • Systolic arterial blood pressure <90 mmHg.
  • History of hypersensitivity and/or idiosyncratic reaction to benzazepine or benzazepine derivatives (such as benazepril).
  • History of drug or medication abuse within the past year,or current alcohol abuse.
  • Uncontrolled diabetes mellitus defined as fasting glucose >300mg/dL.
  • Urinary tract obstruction except BPH if non-obstructive.
  • Previous participation in another clinical drug trial within the past 30 days.
  • Previous participation in this or any other tolvaptan clinical trial.
  • Terminally ill or moribund condition with little chance of short term survival.
  • Serum creatinine >3.5 mg/dL.
  • Serum sodium <120 mEq/L with associated neurologic impairment, i.e. symptoms such as apathy, confusion, seizures.
  • Patients with progressive or episodic neurologic disease such as multiple sclerosis or history of multiple strokes.
  • Child-Pugh score greater than 10 (unless approved)
  • Patients receiving intravenous fluids at a rate greater than KVO (Keep Vein Open).
  • Hyponatremia due to lab artifacts
  • Patients receiving AVP or its analogs for treatment of any condition.
  • Patients receiving within 7 days of randomization, other medications for treatment of hyponatremia specifically: demeclocycline, lithium carbonate or urea
  • Patients likely requiring IV saline for correction of symptomatic or asymptomatic severe hyponatremia during the course of the study.
  • Severe pulmonary artery hypertension
  • Hyponatremia should not be the result of any medication that can safely be withdrawn
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00072683

  Hide Study Locations
Locations
United States, California
VA Greater Los Angeles Health Care Ctr
Los Angeles, California, United States, 90073
UCLA
Los Angeles, California, United States, 93552
UCSF Medical Center
San Francisco, California, United States, 94143
United States, Colorado
University of Colorado Heath Science Center
Denver, Colorado, United States, 80262
Aurora Denver Cardiology Association
Denver, Colorado, United States, 80218
United States, Florida
University of Florida Gainesville
Gainesville, Florida, United States, 32610
Charlotte Heart Group Research Ctr
Port Charlotte, Florida, United States, 33952
United States, Georgia
Medical College of Georgia
Augusta, Georgia, United States, 30912
United States, Illinois
University of Chicago
Chicago, Illinois, United States, 60637
Northwestern University
Chicago, Illinois, United States, 60611
United States, Iowa
University of Iowa Hospital
Iowa City, Iowa, United States, 52242
United States, Minnesota
Minneapolis VA Medical Center
Minneapolis, Minnesota, United States, 55417
United States, Missouri
Washington University Ctr for Clinical Studies
St. Louis, Missouri, United States, 63110
United States, Montana
Mercury Street Medical
Butte, Montana, United States, 59701
United States, New York
Northshore University Hospital
Great Neck, New York, United States
New York, New York, United States, 10010
United States, North Carolina
University of North Carolina, Div. of Cardiology
Chapel Hill, North Carolina, United States, 27599
United States, Ohio
University Hospitals of Cleveland
Cleveland, Ohio, United States, 44106
Ohio State University Medical Center
Columbus, Ohio, United States, 43210
United States, Pennsylvania
The Arthur P. Noyes Research Foundation
Norristown, Pennsylvania, United States, 19401
University of Pittsburgh Medical Center
Pittsburgh, Pennsylvania, United States, 15213
United States, Tennessee
Baptist Clinical Research Ctr
Memphis, Tennessee, United States, 38120
Tennessee Center for Clinical Trials
Tullahoma, Tennessee, United States, 37388
Sponsors and Collaborators
Otsuka Pharmaceutical Development & Commercialization, Inc.
Otsuka Pharmaceutical Co., Ltd.
Investigators
Study Director: Nestor Molfino, MD Otsuka Pharmaceutical Development & Commercialization, Inc.
  More Information

No publications provided by Otsuka Pharmaceutical Development & Commercialization, Inc.

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
ClinicalTrials.gov Identifier: NCT00072683     History of Changes
Other Study ID Numbers: 156-02-235
Study First Received: November 7, 2003
Last Updated: January 24, 2007
Health Authority: United States: Food and Drug Administration

Keywords provided by Otsuka Pharmaceutical Development & Commercialization, Inc.:
Sodium
SIADH
Vasopressin
CHF
Cirrhosis
salt
water
electrolyte

Additional relevant MeSH terms:
Hyponatremia
Inappropriate ADH Syndrome
Water Intoxication
Water-Electrolyte Imbalance
Metabolic Diseases
Pituitary Diseases
Hypothalamic Diseases
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Endocrine System Diseases
Poisoning
Substance-Related Disorders

ClinicalTrials.gov processed this record on April 14, 2014