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Terminated Phase 2 Interventional Results available

A Safety and Efficacy Trial of Stannsoporfin in Neonates With Hyperbilirubinemia

ClinicalTrials.gov ID: NCT00850993

Public ClinicalTrials.gov record NCT00850993. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 5:30 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

It is a normal process in the human body for red blood cells to die, which makes bilirubin. Bilirubin is cleared away through the liver. Some babies are born with livers that don't work well enough yet, or their red blood cells are dying too fast, so the baby looks yellow (jaundice). This means there is too much bilirubin in the body. It can be dangerous if a baby's bilirubin gets too high. Phototherapy is what they call the lights they shine on newborn babies to help the liver get rid of bilirubin. This study tests an experimental drug to see if it can reduce how much bilirubin is being made in the first place.

Study identification

NCT ID
NCT00850993
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Enrollment
58 participants

Conditions and interventions

Eligibility (public fields only)

Age range
1 Minute to 48 Hours
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 2008 (Type not available)
Primary completion
Jun 2011 (Actual)
Completion
May 2012 (Actual)
Last update posted
Oct 30, 2019

2008 – 2012

United States locations

U.S. sites
9
U.S. states
7
U.S. cities
8
Facility City State ZIP Site status
Arrowhead Regional Med Center Colton California 92324 —
UCSD Medical Center San Diego California 92103 —
Kapi'olani Medical Center for Women and Children Honolulu Hawaii 96826 —
University of Louisville Louisville Kentucky 40202 —
Westchester Medical Center Valhalla New York 10595 —
ECU Brody School of Medicine Greenville North Carolina 27834 —
St. Vincent Mercy Children's Hospital Toledo Ohio 43608 —
Drexel University College of Medicine, Clinical Research Group Philadelphia Pennsylvania 19102 —
Albert Einstein Medical Center Philadelphia Pennsylvania 19141 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 14 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00850993, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 30, 2019 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00850993 live on ClinicalTrials.gov.

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