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NCT00869089 · ClinicalTrials.gov registry record · Phase 2

Safety and Efficacy of CC-10004 for Prurigo Nodularis

A Phase 2 study of Prurigo Nodularis, sponsored by University Hospitals Cleveland Medical Center.

Completed
Registry status
Phase 2
Development phase
5
Enrollment target
1
Study location

NCT00869089 is a Phase 2 study of Prurigo Nodularis that has completed, run by University Hospitals Cleveland Medical Center. The registered enrollment target is 5 participants, below the 229-participant average among 14 other Prurigo Nodularis trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00869089, a Phase 2 study of Prurigo Nodularis, has completed, sponsored by University Hospitals Cleveland Medical Center.

COMPLETED
Registry status
Phase 2
Development phase
5 participants
Enrollment target
1
Study location

Study Summary

This trial will include: * Study period up to 7 months. * Office visits monthly lasting approximately 1 hour. * Blood Draws. * Oral medication that is taken 2 times daily. * Photographs and biopsies if agreed.

Conditions Studied

Interventions

  • DRUG CC-10004

Study Locations (1)

Ohio

  • University Hospitals Cleveland Medical Center - Cleveland

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2008-09
Est. Completion 2011-01
Phase Phase 2

What the Registry Record Tells You About NCT00869089

The ClinicalTrials.gov registry entry for NCT00869089 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 5 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 229-participant average among 14 other Prurigo Nodularis trials with a reported enrollment target (98% lower). The listed sponsor is University Hospitals Cleveland Medical Center, which has 230 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Prurigo Nodularis appearing as the primary indexed condition, and to 1 intervention - of which CC-10004 is the first listed.

NCT00869089 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT00869089 about?

NCT00869089 is a clinical study titled "Safety and Efficacy of CC-10004 for Prurigo Nodularis". This trial will include: * Study period up to 7 months. * Office visits monthly lasting approximately 1 hour. * Blood Draws. * Oral medication that is taken 2 times daily. * Photographs and biopsies if agreed.

What is the current status of trial NCT00869089?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 5 participants. The study started on 2008-09. Estimated completion is 2011-01.

What conditions does trial NCT00869089 study?

This clinical trial studies the following conditions: Prurigo Nodularis.

What interventions are being tested in trial NCT00869089?

The interventions under investigation include: CC-10004 (DRUG).

Who is sponsoring clinical trial NCT00869089?

This trial is sponsored by University Hospitals Cleveland Medical Center, which has 230 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00869089 being conducted?

This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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