Efficacy and Safety Study of Tolvaptan to Treat Patients With Cardiac Edema

• ClinicalTrials.gov Identifier: NCT01651156
• Recruitment Status: Completed
• First Posted: July 26, 2012
• Last Update Posted: December 30, 2013
• Sponsor: Otsuka Beijing Research Institute
• Information provided by (Responsible Party): Otsuka Beijing Research Institute

Tracking Information

• First Submitted Date: July 24, 2012
• First Posted Date: July 26, 2012
• Last Update Posted Date: December 30, 2013
• Study Start Date: July 2012
• Actual Primary Completion Date: July 2013 (Final data collection date for primary outcome measure)
• Current Primary Outcome Measures (submitted: July 25, 2012): body weight (change from baseline) [ Time Frame: screening day, Day-3, Day-2, Day-1, Day1, Day2, Day3, Day4, Day5, Day6, Day7, Day8, Day(7+3) ]
• Original Primary Outcome Measures: Same as current
• Current Secondary Outcome Measures (submitted: July 25, 2012): Body weight (percent change from baseline) [ Time Frame: screening day, Day-3, Day-2, Day-1, Day1, Day2, Day3, Day4, Day5, Day6, Day7, Day8, Day(7+3) ]
• Original Secondary Outcome Measures: Same as current
• Current Other Pre-specified Outcome Measures: Not Provided
• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: Efficacy and Safety Study of Tolvaptan to Treat Patients With Cardiac Edema
• Official Title: Randomized, Double-blind, Multicenter, Placebo-controlled, Parallel Phase 3 Study to Evaluate the Efficacy and Safety of Tolvaptan in the Treatment of Patients With Cardiac Edema Based on the Conventional Therapy

Brief Summary

A randomized, double-blind, multicenter, placebo-controlled, parallel study to evaluate the efficacy and safety of Tolvaptan in the treatment of patients with cardiac edema (body fluid retention caused by congestive heart failure) based on the conventional therapy.

To evaluate the efficacy and safety of Tolvaptan 15 mg on congestive heart failure patients with body fluid retention after current diuretic treatment, after continuous treatment of 7 days' oral Tolvaptan 15mg or placebo.

Detailed Description

• A randomized, double-blind, multicenter, placebo-controlled, parallel study
• Study population: The congestive heart failure patients with body fluid retention after received current diuretics therapy
• Number of patients: Patients will be randomly assigned to Tolvaptan and placebo group in 1:1 ratio, 120 patients in each group, 240 patients in total
• Group assignment method: Tolvaptan 15 mg group: conventional therapy + Tolvaptan 15 mg Placebo group: conventional therapy + placebo
• Administration and dosage of the study drug: Once daily, 1 tablet be taken orally after breakfast, for successive 7 days
• Study period:
• Screening period (4 days in minimum, 7 days in maximum), including:

Screening period: from the time the informed consent form is signed to Day -4 Observation period: 3 days before drug administration

• Treatment period: 7 days
• Follow up visits: Day 8 (efficacy evaluation day) and Day 7 (+3) after the last dosing
• Post treatment survey: Day 14 (+3) after the last dosing

• Study Type: Interventional
• Study Phase: Phase 3
• Study Design: Allocation: Randomized; Intervention Model: Parallel Assignment; Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor); Primary Purpose: Treatment
• Condition: Cardiac Edema

Intervention

• Drug: Tolvaptan
  oral taken
  Other Name: Samsca
• Drug: Placebo

Study Arms

• Placebo Comparator: placebo
  Frequency: once per day Duration: 7days
  Intervention: Drug: Placebo
• Experimental: Tolvaptan
  Tolvaptan tablet Frequency: once per day Duration: 7days
  Intervention: Drug: Tolvaptan

• Publications *: Not Provided

Recruitment Information

• Recruitment Status: Completed
• Actual Enrollment (submitted: December 25, 2013): 244
• Original Estimated Enrollment (submitted: July 25, 2012): 240
• Actual Study Completion Date: July 2013
• Actual Primary Completion Date: July 2013 (Final data collection date for primary outcome measure)

Eligibility Criteria

Inclusion Criteria:

• Patients treated with one of the oral diuretic therapy standards （include the patients who will be treated with one of the oral diuretic therapy standards from the beginning of the observation period）:

  1. Only 40 mg/day furosemide taken orally or other oral loop diuretics equivalent to 40 mg/day furosemide note 1)
  2. Combination treatment of oral loop diuretics and thiazide diuretics (no dosage limitation)
  3. Combination treatment of oral loop diuretics and aldosterone antagonists (no dosage limitation)
• Because of the existence of excess body fluid retention, the congestive heart failure patient has at least one of these symptoms (the lower extremity edema, pulmonary congestion note 2), or jugular vein engorgement).
• 20-85 years of age (inclusive) at the time of signing the informed consent document.
• Gender: male or female.
• Inpatients or patient who would be hospitalized from one day before the observation period to the end of efficacy evaluation examination after the last dosing (from Day -4 to the end of efficacy evaluation examination after the last dosing).
• Patient who have signed the informed consent form.

Exclusion Criteria:

• Patients equipped with circulatory assistant device.

• Patients with any of following diseases, complications or symptoms:

  1. Suspected decreased blood volume
  2. Obstructive hypertrophic cardiomyopathy
  3. Severe aortic stenosis
  4. Hepatic coma
• Patients with history of acute myocardial infarction within 30 days prior to screening.
• Patients with diagnosed active myocarditis or amyloid cardiomyopathy.

• Patients with the following diseases, complications or symptoms:

  1. Poorly controlled diabetes with a fasting glucose more than 220 mg/dL (or 12.21 mmol/L)
  2. Anuria
  3. Dysuria caused by urethral stricture, calculus or tumor

• Patients with the following medical history of:

  1. Sustained ventricular tachycardia or ventricular fibrillation within 30 days prior to screening
  2. History of cerebrovascular accident within the past 30 days
  3. Past allergy or hypersensitive reactions to benzodiazepines (e.g. mozavaptan hydrochloride or benazepril hydrochloride)
• Obese patients whose body mass index (BMI = body weight (kg) / height (m)2 ) is more than 35.
• Patients with systolic pressure below 90 mmHg in supine position.

• Patients with any of the following abnormal laboratory test parameters:

  1. Total bilirubin > 2.5 times the upper limits of normal value
  2. Serum creatine > 2.5 times the upper limits of normal value
  3. Serum Na+ > 145 mmol/L (or higher than the upper limits of normal value)
  4. Serum K+ > 5.5 mmol/L
• Patients who unable to take medicine orally.
• Female patients who are pregnant, breast-feeding, at childbearing ages, or with pregnancy plan.
• Patients who participated in clinical trials of other medicine and took other study drugs within 30 days prior to sign the informed consent form.
• Patients who participated in the clinical trial of Tolvaptan and took Tolvaptan previously.
• Patients who have received approved Tolvaptan tablets (Trade name: Samsca) previously.
• Except for the above, patients who were unsuitable to participate in this trial in the investigator's opinion.

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 20 Years to 85 Years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Contacts: Contact information is only displayed when the study is recruiting subjects
• Listed Location Countries: China

Administrative Information

• NCT Number: NCT01651156
• Other Study ID Numbers: 156-12-809-01
• Has Data Monitoring Committee: No
• U.S. FDA-regulated Product: Not Provided
• IPD Sharing Statement: Not Provided
• Responsible Party: Otsuka Beijing Research Institute
• Study Sponsor: Otsuka Beijing Research Institute
• Collaborators: Not Provided

Investigators

• Principal Investigator: Zhang Jian; Fuwai Cardiovascular hospital

• PRS Account: Otsuka Beijing Research Institute
• Verification Date: December 2013