Study of STA-5326 Mesylate in Patients With Moderate to Severe Crohn's Disease

NCT00234741 | Completed Phase 2

• 1 other identifier: 5326-11
• Study Type: interventional
• Target: 12
• Locations: 1 country
• Sites: 1

Brief Summary

STA-5326 is an oral experimental drug that has been shown to block the release of interleukin-12 from peripheral blood mononuclear cells. Given this activity on the immune system, STA-5326 mesylate is a potential treatment for various autoimmune diseases, such as Crohn's disease, that are mediated by the inappropriate expression of Th1 cytokines. This study is evaluating the use of STA-5326 mesylate in patients with moderate to severe, active Crohn's disease. Study visits include a screening visit, 4 treatment period visits over 4 weeks and a follow-up visit that will occur 7 days following the end of treatment. Subjects may continue treatment for an additional 4 weeks of open label STA-5326 mesylate administration that includes an additional 2 treatment period visits. Subjects will undergo a colonoscopy with biopsy collection at baseline, at the end of the 4 week blinded phase and at the end of the 4 week open label phase.

Conditions

Crohn's Disease

Outcome Measures

Primary Outcomes (1)

• To measure the changes from predose in peripheral blood and mucosal cytokines in subjects with active CD after administration of STA-5326 mesylate or placebo for 4 weeks

Secondary Outcomes (9)

• To measure changes in other immunologic parameters.

• To explore the level of cell-surface markers and specific gene expression patterns.

• To measure changes in laboratory surrogate efficacy markers.

• To measure the proportion of subjects in clinical remission at Day 29.

• To measure the proportion of subjects with a clinical response at Day 29.

Interventions

STA-5326 mesylate DRUG

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Is male or female aged 18 through 75 years.
• Has Crohn's disease diagnosed definitively prior to Screening (based upon clinical, endoscopic, radiologic imaging, or histological assessments).
• Has a CDAI score of 220 to 450, inclusive at Baseline.

You may not qualify if:

• Has any clinically significant disease (eg, renal, hepatic, neurological, cardiovascular, pulmonary, endocrinologic, psychiatric, hematologic, urologic, or other acute or chronic illness) that in the opinion of the investigator would make the subject an unsuitable candidate for this study.
• Is a woman who has a positive pregnancy test, who is breast-feeding, or who is sexually active without using birth control during the course of the study and Follow-up period.
• Is a woman of childbearing potential or a man who does not agree to use 2 forms of contraception during the course of the study and Follow-up period.
• Has clinically significant hematologic, hepatic or renal laboratory abnormalities.

Sponsors & Collaborators

• Synta Pharmaceuticals Corp.: lead
• National Institute of Allergy and Infectious Diseases (NIAID): collaborator
• National Institutes of Health (NIH): collaborator

Study Sites (1)

Nih/Niaid

Bethesda, Maryland, 20892, United States

Location

MeSH Terms

Conditions

Crohn Disease

Interventions

apilimod

Condition Hierarchy (Ancestors)

Inflammatory Bowel Diseases; Gastroenteritis; Gastrointestinal Diseases; Digestive System Diseases; Intestinal Diseases

Study Officials

• Peter Mannon, MD

  National Institute of Allergy and Infectious Diseases (NIAID)

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY

Study Record Dates

• First Submitted: October 5, 2005
• First Posted: October 7, 2005
• Study Start: November 1, 2005
• Last Updated: December 4, 2008

Record last verified: 2008-12

Locations

US (1)