Effect of Anti-Inflammatory Agents on Biological Responses to Endotoxin Inhalation in Healthy Subjects

• Status: Completed
• Trial end date: 2009-07-01
• Target enrollment: 0
• Participant gender: All

Summary

The main objective of this study is to characterize the biological responses elicited by endotoxin inhalation applied to healthy subjects, and to assess the effect of standard anti-inflammatory agents (i.e. adalimumab and methylprednisolone) on these biological responses.

• Phase: Early Phase 1
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Brugmann University Hospital
• Treatments: Adalimumab; Anti-Inflammatory Agents; Methylprednisolone; Methylprednisolone Acetate; Methylprednisolone Hemisuccinate; Prednisolone; Prednisolone acetate; Prednisolone hemisuccinate; Prednisolone phosphate

Criteria

Inclusion Criteria:

1. Male or female aged 18 to 49 years, inclusive.

2. Responsive to inhaled endotoxin; defined as a reduction of 10% or greater in forced expiratory volume in 1 second (FEV1) following inhalation of 20 µg equivalent of Clinical Center Reference Endotoxin.

3. Have a body weight greater than 65 kg and a body mass index (BMI) below 30.

4. Have normal lung function, defined as:

• Forced vital capacity (FVC) > 80% of that predicted value;

• FEV1 > 80% of that predicted value; and

• FEV1/FVC ratio > 80% of predicted values.

5. Have vital signs within the normal range, as follows:

• Oral body temperature: 35.0 to 36.5 °C.

• Blood pressure (BP):

• After at least 3 minutes of rest, measured in the supine position:

• Systolic BP: 90 to 140 mm Hg.

• Diastolic BP: 50 to 90 mm Hg.

• Then, after 1 minute standing:

• Systolic BP: no more than a 20 mmHg decrease.

• Diastolic BP: no more than a 10 mm Hg decrease.

• Heart rate: after at least 3 minutes of rest and measured in the supine position:

40 to 90 beats per minute (bpm).

6. Have a hemoglobin level of 12.0 g/dL or more.

7. Have been a non-smoker for the preceding 12 months.

8. Willing and able to give written informed consent and to comply with the requirements of the study.

9. Female subjects must not be pregnant or lactating.

10. All subjects who are sexually active must use a medically acceptable and highly effective method of birth control for the duration of the study, and continue for 90 days after the end of treatment.

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Exclusion Criteria:

1. Have any condition, including findings in the medical history or in the pre-study assessments, which, in the opinion of the investigator, constitute a risk or contraindication for the participation of the subject to the study, or that could interfere with the study objectives, conduct, or evaluation including, but not limited to:

• Any clinically significant abnormality in the results of pre-study safety laboratory tests.

• A positive test for drugs of abuse or alcohol breath test.

• Positive results from serum tests for Hepatitis B surface antigen (not due to vaccination), Hepatitis C, or Human Immunodeficiency Virus.

• History or presence of lung disease including asthma, chronic obstructive lung disease, or emphysema.

• History of atopy, including hay fever or atopic dermatitis.

• History or presence of liver disease.

• Hyperthyroidism, hypoglycemia, hyperglycemia, or diabetes mellitus.

• History or presence of autoimmune disorders including myositis, hepatitis, idiopathic thrombocytopenic purpura, psoriasis, rheumatoid arthritis, interstitial nephritis, Sjögren's syndrome, thyroiditis, or systemic lupus erythaematosus.

• Occurrence of any acute infection within the last 2 weeks before dosing.

2. Presence or history of any severe allergic reactions; or history of allergy to any medications that may be used or prescribed in the course of this study (eg, albuterol, prednisolone, acetaminophen, aspirin or other non-steroidal anti-inflammatory agents, or adalimumab).

3. History or presence of drug or alcohol abuse. (i;e. average daily intake of 3 units or a maximum weekly intake of greater than 21 units (1 unit equals 340 milliliters [ml] of beer, 115 ml of wine, or 43 ml of spirits).

4. History or active manifestation of a serious psychiatric illness including depression, suicidal ideation, or psychosis.

5. Positive test for latent tuberculosis.

6. Loss or donation of blood within 12 weeks prior to entry into the study, or plasma donation within 1 week prior to entry into the study.

7. Use of any prescription drugs within 2 weeks or over-the-counter medication, including herbal supplements or multivitamins, within 1 week before drug administration without prior approval from the investigator.

8. Use of any medication that may impact the results of any of the challenges, interfere with any other medications potentially used in the study, including steroids, beta blockers, or non-steroidal anti-inflammatory agents.

9. Previous participation in this study, or administration of any investigational drug within 12 weeks prior to entry into the study.

10. Exposure to endotoxin, within 12 weeks of signing the informed consent for this study.

11. History of exposure to keyhole limpet hemocyanin (KLH), dog rabies vaccine, or history of immunization with inactivated Hepatitis A virus.

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