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Completed Phase 3 Interventional Results available

An Open-Labeled, Extended-Use of XERECEPT (hCRF) for Patients in Studies NTI 0302, 0303, or Other Designated Studies

ClinicalTrials.gov ID: NCT00226655

Public ClinicalTrials.gov record NCT00226655. 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 30, 2026, 1:37 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

An Open-Labeled, Extended-Use of Human Corticotropin-Releasing Factor (hCRF) Intended for Patients Who Participate in Dexamethasone-Sparing Studies NTI 0302, NTI 0303, or Other Designated Studies

Brief summary

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

The purpose of this study is to examine the long-term safety and tolerability of human corticotropin-releasing factor (hCRF), XERECEPT®, in patients requiring dexamethasone (Decadron) to treat peritumoral brain edema. This open-label, extended-use study is open to all patients who participate in either of the blinded studies, NTI 0302, NTI 0303, or other designated studies, including patients who may have discontinued blinded study medication early but completed the protocol-stipulated follow-up periods.

Study identification

NCT ID
NCT00226655
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
112 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
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
Jul 2005 (Type not available)
Primary completion
Mar 2009 (Actual)
Completion
Apr 2009 (Actual)
Last update posted
Aug 31, 2012

2005 – 2009

United States locations

U.S. sites
25
U.S. states
13
U.S. cities
23
Facility City State ZIP Site status
Barrow Neurological Institute Phoenix Arizona 85013 —
Hoag Memorial Hospital Presbyterian Newport Beach California 92658 —
Stanford University Medical Center Palo Alto California 94305 —
UC Davis Medical Center, Division of Medical Oncology Sacramento California 95817 —
UC San Diego Cancer Center San Diego California 92037 —
University of Colorado Cancer Center Aurora Colorado 80045 —
Colorado Neurological Institute Center for Brain & Spinal Tumors Englewood Colorado 80113 —
Mayo Clinic Jacksonville Florida 32224 —
Cancer Institute of Orlando Orlando Florida 32804 —
Moffitt Cancer Center Tampa Florida 33612 —
Winship Cancer Institute, Emory University Atlanta Georgia 30322 —
Feinberg School of Medicine, Northwestern University Chicago Illinois 60611 —
Evanston Northwestern Healthcare Evanston Illinois 60201 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Hermelin Brain Tumor Center, Henry Ford Hospital Detroit Michigan 48202 —
Dent Neurologic Institute Amherst New York 14226 —
Memorial Sloan Kettering Cancer Center New York New York 10021 —
Weill Medical College of Cornell University New York New York 10021 —
University Hematology Oncology Care, LLC Cincinnati Ohio 43210 —
Good Samaritan Hospital Cincinnati Ohio 45220 —
The Ohio State University Columbus Ohio 43210 —
Oregon Clinic Portland Oregon 97210 —
Virginia Mason Clinic Seattle Washington 98111 —
University of Wisconsin Madison Wisconsin 53792 —
Medical College of Wisconsin Milwaukee Wisconsin 53226-3596 —

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 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00226655, 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 Aug 31, 2012 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00226655 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →