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Completed Phase 4 Interventional Results available

Study Evaluating Two Dose Levels of Targretin Capsules in Participants With Refractory Cutaneous T-Cell Lymphoma (CTCL)

ClinicalTrials.gov ID: NCT01007448

Public ClinicalTrials.gov record NCT01007448. 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 Sep 2, 2026, 4:49 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

Phase IV Randomized Study of Two Dose Levels of Targretin® Capsules in Subjects With Refractory Cutaneous T-Cell Lymphoma

Brief summary

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

This is a multicenter, randomized, open-label, Phase IV study to assess the efficacy, tolerability, and safety of 2 initial dose levels of bexarotene capsules in participants with refractory CTCL.

Study identification

NCT ID
NCT01007448
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Bausch Health Americas, Inc.
Industry
Enrollment
59 participants

Conditions and interventions

Interventions

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
Jan 5, 2010
Primary completion
Feb 19, 2014
Completion
Feb 19, 2014
Last update posted
Nov 11, 2019

2010 – 2014

United States locations

U.S. sites
17
U.S. states
15
U.S. cities
17
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35233
Florida Academic Dermatology Centers Miami Florida 33136
Emory University Atlanta Georgia 30322
Rush University Chicago Illinois 60612
Tulane New Orleans Louisiana 70112
University of Michigan Ann Arbor Michigan 48109
University of Minnesota Medical School Minneapolis Minnesota 55455
Washington University St Louis Missouri 63110
University of Rochester Rochester New York 14642
Duke University Durham North Carolina 27710
Wake Forest University Health Winston-Salem North Carolina 27157
University Hospitals-Case Medical Center Cleveland Ohio 44106
University of Pittsburgh Pittsburgh Pennsylvania 15213
Vanderbilt Nashville Tennessee 37206
University of Texas Southwestern Medical Center Dallas Texas 75390
MD Anderson Cancer Center Houston Texas 77030
Huntsman Cancer Institute At the University of Utah Salt Lake City Utah 84112

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01007448, 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 Nov 11, 2019 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01007448 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →