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Deland, Florida 32720


Purpose:

The proposed study aims to compare the pharmacokinetics and bioavailability of intravenous and subcutaneous Furosemide. Although these regimens are not intended to be bioequivalent, they are both expected to achieve therapeutic plasma levels and induce effective diuresis. The test formulation in this study is a buffered solution, Furosemide Injection Solution at 8 mg/mL at pH 7.4 (range 7.0 to 7.8) and is intended for SC injection according to the instructions in the protocol. A commercial formulation of Furosemide Injection, USP will serve as the reference drug in this study, which will be administered by IV bolus. It contains furosemide 10 mg/mL in solution at alkaline pH of 8.0 to 9.3 and is marketed for IV and IM injection. The objectives of this study are: - To characterize the pharmacokinetics of furosemide administered by continuous subcutaneous infusion using a biphasic delivery profile. - To estimate the absolute bioavailability of furosemide administered by continuous subcutaneous infusion compared with an equivalent dose of furosemide administered by intravenous bolus administration.


Study summary:

This study will be an open-label, single-center, single-dose, randomized, two-way (two-period) crossover study in 16 adult subjects previously diagnosed with mild to moderate heart failure (NYHA class II/III) being treated concomitantly with oral furosemide therapy at a dose of ≥ 40 mg/day. Each subject will complete Screening, Baseline, Treatment, and Follow-Up Phases. The Screening Phase will be conducted on an outpatient basis between 14 and 3 days prior to Baseline. Subjects will be instructed to maintain a < 2 gm sodium diet within 3 days prior to Baseline. Baseline (Day 0) consists of clinical research unit (CRU) admission and final qualification assessments. The Treatment Phase will comprise two crossover periods separated by a 7-day outpatient fluid re-equilibration washout. Following CRU admission, subjects will discontinue oral furosemide at least 24 hours prior to administration of study drug for each Crossover Period. Subjects will be randomly assigned in a 1:1 ratio to 1 of 2 treatment sequences to receive both intravenous (IV) and subcutaneous (SC) furosemide in Crossover Periods (i.e., IV followed by SC or vice versa). Subjects will remain domiciled in the CRU for each Crossover Period during the Treatment Phase through 24 hours after administration of study drug, after which time they will be discharged if safety parameters are acceptable to the Investigator. Oral furosemide therapy will be re-initiated at discharge after Crossover Period 1 (i.e., during the 7-day fluid re-equilibration washout) and after Crossover Period 2. The Follow-Up Phase will occur 7 days (± 1) after discharge from the CRU following Crossover Period 2, completing subjects' study participation.


Criteria:

Inclusion Criteria: - An Institutional Review Board (IRB) approved informed consent is signed and dated prior to any study-related activities. - Male and female subjects ≥18 years of age, with body volume and weight <130 kg and body mass index (BMI) <38 kg/m2 - Females will be non-pregnant, non-lactating, and post-menopausal, surgically sterile (e.g., tubal ligation, hysterectomy), or use TWO (2) of the following forms of contraception: IUD, IUD with spermicide, female condom with spermicide, contraceptive sponge with spermicide, an intravaginal system, diaphragm with spermicide, cervical cap with spermicide, a male sexual partner who agrees to use a male condom with spermicide, a sterile sexual partner, OR abstinence - History of at least 3 months treated heart failure (NYHA class II/III) with presence of symptoms of chronic volume overload requiring ongoing treatment with oral furosemide at a dose of ≥ 40 mg per day for at least 30 days prior to baseline - NT-proBNP > 300 pg/mL or BNP > 100 pg/mL - Agrees to abstain from using alcohol, caffeine-containing products, and tobacco-/nicotine-containing products through CRU discharge (period 2). - Able to participate in the study in the opinion of the investigator - Has the ability to understand the requirements of the study and is willing to comply with all study procedures Exclusion Criteria: - Acute Decompensated Heart Failure (ADHF) or recent history of hospitalization for heart failure in the last 4 weeks - Worsening of signs or symptoms of heart failure in the two weeks prior to the Screening, or those expected to require intravenous loop diuretics or in-patient treatment for heart failure during the study - Systolic BP (SBP) < 90 mm Hg - Temperature > 38°C (oral or equivalent) or sepsis or active infection requiring IV anti-microbial treatment - Serum sodium < 130 mEq/L and Serum potassium < 3.0 mEq/L - Significant other cardiac abnormalities which may interfere with study participation or study assessments - Current or planned treatment during the study with any IV therapies, including inotropic agents, vasopressors, levosimendan, nesiritide or analogues; or mechanical support (intra-aortic balloon pump, endotracheal intubation, mechanical ventilation, or any ventricular assist device) - Diagnosed with Type I diabetes mellitus or Type II diabetes requiring insulin therapy - Presence or need for urinary catheterization, urinary tract abnormality, or disorder interfering with urination - Impaired renal function, defined as an estimated glomerular filtration rate (eGFR) on admission < 45 mL/min/1.73m2, calculated using the simplified Modification of Diet in Renal Disease (sMDRD) equation - Indication of moderate-to-severe hepatic dysfunctions as determined by the investigator - Administration of intravenous radiographic contrast agent within 72 hours prior to Screening or acute contrast-induced nephropathy at the time of Screening - Major surgery within 30 days prior to Screening - Administration of an investigational drug or implantation of investigational device, or participation in another interventional trial, within 30 days prior to Screening - Any surgical or medical condition which in the opinion of the investigator may interfere with participation in the study or which may affect the outcome of the study - Positive test for hepatitis B, hepatitis C, or HIV at Screening - Positive urine drug screen at Screening or Baseline - Concomitant use of any drugs known to interact with furosemide - History of alcohol abuse within 6 months prior to screening, as determined by the Investigator - Positive alcohol breath test on admission to the CRU - History of severe allergic or hypersensitivity reactions to furosemide - Donation of greater than 100 mL of either whole blood or plasma within 30 days prior to study drug administration


NCT ID:

NCT02329834


Primary Contact:

Principal Investigator
Bruce G. Rankin, DO, CPI, MRO, FACOFP
Avail Clnical Research, LLC


Backup Contact:

N/A


Location Contact:

Deland, Florida 32720
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 22, 2017

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