Alicaforsen (ISIS 2302) in Patients With Active Crohn's Disease

NCT ID: NCT00048295

Last Updated: 2022-08-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

150 participants

Study Classification

INTERVENTIONAL

Study Start Date

2002-05-31

Brief Summary

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ISIS 2302 is an antisense oligonucleotide drug that reduces the production of a specific protein called intercellular adhesion molecule (ICAM-1), a substance that plays a significant role in the increase of inflammation. People with Crohn's disease have been shown to over-produce ICAM-1 in their gut tissues. Alicaforsen works by blocking ICAM-1 messenger RNA, the "instruction" molecule that is required for the production of ICAM-1 protein. This trial will examine effects of alicaforsen delivered by 2-hour intravenous infusion over a four-week period, compared to a placebo. Patients may remain on stable background 5-ASA, antibiotic, or immunosuppressive drugs, and prednisone (or equivalent) at \</= 30 mg per day.

Detailed Description

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Conditions

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Crohn's Disease

Study Design

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Allocation Method

RANDOMIZED

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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Alicaforsen

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

1. Age \>/= 12 years
2. Weight \>/= 36 kg
3. CDAI score of 220 - 400
4. Documentation of Crohn's disease activity by endoscopy, biopsy or imaging in the last 2 years
5. No TNF-α inhibitor treatment for three months prior to first study drug infusion

Exclusion Criteria

1. Known severe, fixed, symptomatic stenosis of the small or large intestine with significant dilation
2. Extensive external fistulization (\> 3 external fistulae which are expressible with gentle compression); colostomy or ileostomy
3. Active infection, including infectious colitis, or infection with HIV, Hepatitis B or Hepatitis C
4. Malignancy within 3 years or poorly controlled medical illness
5. Requires intravenous heparin therapy or with a history of a bleeding problem
Minimum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ionis Pharmaceuticals, Inc.

INDUSTRY

Sponsor Role lead

Locations

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Kortrijk, , Belgium

Site Status

Roeselare, , Belgium

Site Status

Hradic Kralove 2, , Czechia

Site Status

Olomouc, , Czechia

Site Status

Prague, , Czechia

Site Status

Ústí nad Orlicí, , Czechia

Site Status

Minden, , Germany

Site Status

Münster, , Germany

Site Status

Torino, , Italy

Site Status

Krakow, , Poland

Site Status

Szczecin, , Poland

Site Status

Warsaw, , Poland

Site Status

Wroclaw, , Poland

Site Status

Barcelona, , Spain

Site Status

Valencia, , Spain

Site Status

Countries

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Belgium Czechia Germany Italy Poland Spain

Related Links

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http://www.centerwatch.com

Type "ISIS 2302" in search box

http://www.acurian.com

Type "ISIS 2302" in search box, then click on "Crohn's Disease Alicaforsen Investigation"

Other Identifiers

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ISIS 2302-CS21

Identifier Type: -

Identifier Source: org_study_id

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