A Clinical Trial Evaluating the Safety and Effectiveness of Golimumab in Patients With Severe, Persistent Asthma

NCT ID: NCT00675649

Last Updated: 2015-04-10

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE2
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-05-31

Brief Summary

The purpose of this study is to assess the safety and effects (good and bad) of golimumab therapy in patients with severe, persistent asthma.

Detailed Description

Golimumab is a type of tumor necrosis factor (TNF) inhibitor. TNF is a naturally occurring substance in the body and this substance may cause long-term inflammation. Golimumab may help treat this disease by blocking the activity of TNF in the body and reducing the symptoms of severe, persistent asthma.This study will assess the safety and effectiveness of subcutaneously (under the skin) administered golimumab and determine if there is a reduction of signs and symptoms in patients with active severe, persistent asthma. The effect of subcutaneously (SC) administered golimumab on the quality of life in patients with severe, persistent asthma will also be assessed. About 200 patients will take part in the study at approximately 60 centers worldwide. Participation in the study will last for about 42 weeks. The study consists of 3 phases: the screening phase (lasting between 1 and 4 weeks), the treatment phase (20 weeks), and the follow-up phase (20 weeks). Visits are scheduled to occur once every 4 weeks during the treatment and follow-up phases of the study. Patients eligible to take part in this study will be randomly placed into one of the following study groups: Group 1: Placebo (an inactive or dummy treatment that looks the same as the study drug, golimumab, but does not contain any active medication) from Week 0 through Week 20. Group 2: Golimumab 100 mg from Week 0 through Week 20. This study is "blinded." This means that neither patient nor study doctor will know in which group a patient is placed. However, if needed for safety or health reasons, the study doctor can find out a patient's study group at any time.

Patients will receive an injection (under the skin) of placebo (Group 1) or golimumab 100 mg (Group 2) every 4 weeks from Week 0 through Week 20.

Conditions

Asthma

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

001

Group Type: EXPERIMENTAL

CNTO 148 / Golimumab

Intervention Type: BIOLOGICAL

100 mg sc injection every 4 weeks from week 0 to week 20

002

Group Type: PLACEBO_COMPARATOR

placebo

Intervention Type: BIOLOGICAL

placebo sc injection every 4 weeks from week 0 to week 20

Interventions

CNTO 148 / Golimumab

100 mg sc injection every 4 weeks from week 0 to week 20

Intervention Type: BIOLOGICAL

placebo

placebo sc injection every 4 weeks from week 0 to week 20

Intervention Type: BIOLOGICAL

Eligibility Criteria

Inclusion Criteria

• Physician diagnosis of asthma for >= 3 years and a diagnosis of severe, persistent asthma for >= 1 year prior to screening
• Reversible airway obstruction
• Continuous treatment with high dose inhaled corticosteroids and long-acting Beta2-agonist for at least 3 months prior to screening
• At least 1 occasion in the previous 6 months when worsening of asthma required treatment with additional steroids (intravenous or oral)
• Score of >= 2 points on the Asthma Control Questionnaire (ACQ) at screening

Exclusion Criteria

• Diagnosis of chronic obstructive pulmonary disease (COPD), cystic fibrosis, or other significant respiratory disorder
• Life-threatening asthma attack requiring intubation in the 6-month period prior to screening
• Steroid use at a dose > 20 mg of prednisone at the screening visit
• Known malignancy or history of malignancy
• Previous exposure to anti-TNF therapies

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Centocor, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Centocor, Inc. Clinical Trial

Role: STUDY_DIRECTOR

Centocor, Inc.

Other Identifiers

C0524T26

Identifier Type: -

Identifier Source: secondary_id

EudraCT No.: 2007-005699-15

Identifier Type: -

Identifier Source: secondary_id

CR014980

Identifier Type: -

Identifier Source: org_study_id