Efficacy Study of Humira in the Treatment of Cutaneous Sarcoidosis

NCT00731757 · Status: WITHDRAWN · Phase: PHASE2 · Type: INTERVENTIONAL

Last updated 2022-02-15

No results posted yet for this study

Summary

The purpose of this study is to determine the safety and efficacy of Humira in the treatment of cutaneous sarcoidosis.

Conditions

  • Sarcoidosis
  • Cutaneous Sarcoidosis

Interventions

DRUG

Humira

80 mg at week 0, then 40 mg weekly from week 1-week 23.

Sponsors & Collaborators

Principal Investigators

  • Michael P Heffernan, MD · Wright State University

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-05-31
Primary Completion
2010-12-31
Completion
2010-12-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00731757 on ClinicalTrials.gov