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A Phase 2b, Multicenter, Single-dose, Blinded, Randomized, Placebo-controlled, Dose-escalation, Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia

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City:   Cincinnati
State:   Ohio
Zip Code:   45229
Conditions:   Hyperbilirubinemia, Neonatal
Purpose:   The purpose of this study is to determine if an experimental drug, Stanate®, is safe and effective in the treatment of hyperbilirubinemia in hemolyzing neonates.
Study Summary:  
Criteria:   Inclusion Criteria: - Term and late preterm subjects - Risk factors for hemolytic disease to include ABO blood type incompatibility or Rh incompatibility (anti-C, c, D, E, or e, or G6PD deficiency - A minimum birth weight of 2500 g (5.5 lbs) - Enrollment within 2 mg/dL below the TSB threshold for PT per the AAP Guidelines at up to 12 hours of age or within 3 mg/dL below the threshold for PT at >12 to 48 hours of age, inclusive - Randomization and treatment cannot take place until the infant is within 1 mg/dl below the threshold for PT per the AAP Guidelines at up to 12 hours of age or within 2 mg/dL below the threshold for PT at >12 to 48 hours of age, inclusive Exclusion Criteria: - Treatment or need for treatment in the neonate with medications that may prolong the QT interval, family history of Long QT syndrome or family history of Sudden Infant Death Syndrome - Risk factors for porphyrias, including family history - Apgar score ≤6 at age 5 minutes - Significant congenital anomalies or infections - Cardiorespiratory distress - Any abnormal auditory or ophthalmologic findings - Any excess risk of requiring surgery or exposure to operating room lights in the foreseeable future - Clinically significant abnormalities on screening laboratory evaluation - Use of photosensitizing drugs or agents - Use of intravenous immunoglobulin (IVIG) or albumins - Other serious morbid conditions, eg, pulmonary disease, cardiovascular disease
NCT ID:   NCT00850993
Primary Contact:   Principal Investigator
M. Jeffrey Maisels, MB, BCh
William Beaumont Hospitals

Warren W. Wasiewski, M.D.
Phone: 267.515.5861
Email: wwasiewski@infacare.com
Backup Contact:   N/A
Location Contact:   Cincinnati, Ohio 45229
United States



There is no listed contact information for this specific location.

Site Status: Withdrawn

Data Source:   ClinicalTrials.gov
Date Processed:   May 23, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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