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Terminated Phase 3 Interventional

Study of Human Monoclonal Antibody to Treat Mycosis Fungoides and Sezary Syndrome

ClinicalTrials.gov ID: NCT00127881

Public ClinicalTrials.gov record NCT00127881. 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 Jul 21, 2026, 9:49 AM EDT

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

Official title

Open Label, Dose Escalation, Followed by Open Label,Single Arm Clinical Trial of HuMax-CD4 in Patients With Mycosis Fungoides Type CTCL (Stage IB-IVB) or Sezary Syndrome Who Are Refractory or Intolerant to Targretin® (Bexarotene) and One Other Standard Therapy

Study identification

NCT ID
NCT00127881
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Emergent Product Development Seattle LLC
Industry
Enrollment
76 participants

Conditions and interventions

Interventions

  • HuMax-CD4 (zanolimumab) Drug

Drug

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
Jun 30, 2005
Primary completion
Jan 31, 2014
Completion
Not listed
Last update posted
Jul 25, 2012

Started 2005

United States locations

U.S. sites
19
U.S. states
16
U.S. cities
18
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama
Stanford University Medical Center Stanford California 94305
University of Colorado Aurora Colorado 80045
H. Lee Moffitt Cancer Center Tampa Florida 33612
The Emory Clinic Atlanta Georgia 30322
Northwestern University Chicago Illinois 60611
Tulane University Health Science Center New Orleans Louisiana 70112
Boston Medical Center Boston Massachusetts 02118
University of Michigan Medical Center Ann Arbor Michigan 48109
New York Medical Center New York New York 10016
Memorial Sloan Kettering New York New York 10021
SUNY Upstate Medical University Syracuse New York 13210
Duke University Medical Center Durham North Carolina 27710
University Hospital of Cleveland Cleveland Ohio 44106
Ohio State University Columbus Ohio 43201
Oregon Health & Science University Portland Oregon 97239
University of Pennsylvania Health System Philadelphia Pennsylvania 19104
Middle Tennessee Research Institute Nashville Tennessee 37212-2637
MD Anderson Cancer Center Houston Texas 77030

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 16 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00127881, 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 Jul 25, 2012 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00127881 live on ClinicalTrials.gov.

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