TNF-Alpha Directed Therapy in Asthma
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Purpose
This trial is a randomised, single-center, placebo-controlled, double blind, parallel group study in patients with asthma symptomatic on inhaled steroids.
This trial will examine the efficacy and safety of 5 mg/kg doses of infliximab in patients with inhaled corticosteroid-dependent asthma. The primary objective of this study is to obtain pharmacological evidence for a role of the pro-inflammatory cytokine TNF-alpha in patients with asthma symptomatic on inhaled steroids and to evaluate the safety and tolerability of repeated intravenous administration of infliximab.
| Condition | Intervention | Phase |
|---|---|---|
|
Asthma |
Drug: Study drug administration Procedure: Tuberculin intradermal skin test Procedure: Lung function test for FEV1 Procedure: Asthma symptom scores diary Procedure: Quality of life diary Procedure: Breath nitric oxide Procedure: Breath condensate Procedure: Sputum induction Procedure: Blood sampling Procedure: Urinalysis |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double-Blind Primary Purpose: Treatment |
| Official Title: | A Randomised, Double Blind, Placebo-Controlled, Parallel Group Pilot Study to Determine the Effect of REMICADE on Safety, Efficacy and Biomarkers of Inflammation in Patients With Asthma Receiving Inhaled Corticosteroids |
- Change from baseline (prior to visit 4: days –7 to –1) to week 8 (prior to visit 8: days 49-56) in mean morning PEFR from clinical diaries:
- The morning PEFR for a 7 day period (week 7 to 8) will be compared to the 7 day period prior to first administration (days –7 to –1).
- 1. Evening PEFR
- 2. FEV1 from clinical diaries and on study visits
- 3. Diurnal variation in PEFR
- 4. Symptoms score
- 5. Short-acting beta2-agonist usage = rescue salbutamol
- 6. Exacerbation’s and episode-free days
- 7. Quality of life (St. George’s Respiratory Questionnaire)
- 8. Exhaled breath NO and breath condensates
- 9. Sputum levels of IL-8, TNF-alpha and eotaxin (in supernatant) and differential white cell count
- 10. Peripheral blood eosinophil count, and total IgE
- 11. Expression of mRNA related to inflammation in peripheral blood
| Estimated Enrollment: | 40 |
| Study Start Date: | October 2001 |
| Estimated Study Completion Date: | April 2004 |
Show Detailed Description
Eligibility| Ages Eligible for Study: | 18 Years to 60 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Have a diagnosis of moderate asthma as defined by the American Thoracic Society criteria (NIH, 1997) for > 1 year.
- Men and women, >/= 18 to </= 60 years of age and within 60-140% of desirable height and weight range established by the 1983 Metropolitan Life Insurance Company standards.
- Non-smoker for at least 1 year and less than a 10 pack year history of smoking.
- Screening values for haematology, biochemistry and urinalysis should be within clinically acceptable limits for this patient group.
- Chest radiograph at screening must show no evidence of malignancy, infection, or fibrosis. The chest radiographs should also show no apical scarring, cavitary lesions, or calcified granulomas, as evidence of past tuberculosis infections.
- Serological assays for hepatitis B and C must be negative for active infection.
Exclusion Criteria:
- Are pregnant, nursing, or planning a pregnancy within 12 months of enrolment.
- Diagnosis of chronic obstructive pulmonary disease, cystic fibrosis or other significant respiratory disorder (excluding asthma).
- Exacerbation of asthma symptoms requiring hospitalisation within the previous 12 weeks.
- History of clinically significant seasonal allergies will require that the patient is studied outside the allergy season.
- Have been previously treated with infliximab or any other therapeutic agent targeted at reducing TNF.
- Have been treated with any anti-CD-4 antibody.
- Have been treated with any investigational drug within the previous 3 months or within 5 half-lives, whichever is greater.
- Have previously used cyclophosphamide, nitrogen mustard, chlorambucil, or other alkylating agents.
- Have a history of any clinically significant adverse reaction to murine or chimeric proteins, including but not limited to allergic reactions.
11. Have had a serious infection during the previous 2 months. 12. Have a chronic or recurrent infectious disease 13. Have a history of opportunistic infections 14. Have current signs or symptoms of severe, progressive or uncontrolled renal, hepatic, hematologic, gastrointestinal, endocrine, pulmonary, cardiac, neurologic, or cerebral disease.
15. Have a history of lymphoproliferative disease, including lymphoma 16. Currently have any known malignancy or have a history of malignancy within the previous 5 years.
17. Have had substance abuse (drug or alcohol) problem within the previous 10 years.
18. Use of restricted respiratory medication prior to screening within the following time periods: 1) oral or systemic steroids, 1 month; 2) immunosuppressant therapy, 3 months.
19. Have a history of chronic cough, haemoptysis, weight loss, or pyrexia considered suggestive of possible current tuberculosis infection.
20. Patients with current active tuberculosis (TB) or atypical mycobacterial infection or a previous history of these infections.
21. Be considered at high risk for tuberculosis according to US Centers for Disease Control and Prevention (CDC) criteria, 22. A tuberculin (purified protein derivative, PPD) intradermal skin test > 10mm induration.
23. Have demyelinating disease (multiple sclerosis), autoimmune conditions such as systemic lupus.
Contacts and Locations| United Kingdom | |
| NHLI Clinical Studies Unit | |
| London, United Kingdom, SW3 6HP | |
| Principal Investigator: | Trevor T Hansel, FRCPath PhD | Imperial College London |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00278083 History of Changes |
| Other Study ID Numbers: | C0168T42 |
| Study First Received: | January 17, 2006 |
| Last Updated: | January 17, 2006 |
| Health Authority: | United Kingdom: Research Ethics Committee |
Keywords provided by Imperial College London:
|
Pharmacology Asthma TNF-alpha |
Additional relevant MeSH terms:
|
Asthma Bronchial Diseases Respiratory Tract Diseases Lung Diseases, Obstructive Lung Diseases Respiratory Hypersensitivity Hypersensitivity, Immediate Hypersensitivity Immune System Diseases Nitric Oxide Bronchodilator Agents Autonomic Agents Peripheral Nervous System Agents |
Physiological Effects of Drugs Pharmacologic Actions Anti-Asthmatic Agents Respiratory System Agents Therapeutic Uses Free Radical Scavengers Antioxidants Molecular Mechanisms of Pharmacological Action Neurotransmitter Agents Endothelium-Dependent Relaxing Factors Vasodilator Agents Cardiovascular Agents Protective Agents |
ClinicalTrials.gov processed this record on May 23, 2013