A Study to Investigate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single and Repeat Doses of CHF6297 in Healthy Subjects and Patients With COPD (CHF6297 FIH)

Chiesi

Status and phase: Terminated; Phase 2; Phase 1

Conditions: Chronic Obstructive Pulmonary Disease

Treatments: Drug: CHF6297 (Part 1 - SAD); Drug: CHF6297 (Part 3); Drug: CHF6297 (Part 2 - MAD); Drug: Placebo (Part 3); Drug: CHF6297 (Part 4); Drug: Placebo (Part 4); Drug: Placebo (Part 1 - SAD); Drug: Placebo (Part 2 - MAD)

Study type: Interventional

Funder types: Industry

Identifiers

NCT02815488

CCD-06297AA1-01

2015-003075-30 (EudraCT Number)

Details and patient eligibility

About

CHF6297 is a potent and selective inhibitor of human MAP kinase p38 being developed as an anti-inflammatory agent for the treatment of inflammatory airways diseases. The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of single and repeat doses of CHF6297 as dry powder formulation in healthy subjects and in COPD patients. This study is the first administration in humans.

The study will comprise four parts:

Part 1 will consist of two cohorts of healthy male subjects to assess the safety, tolerability and pharmacokinetics of Single Ascending Dose (SAD) of CHF6297.

Part 2 will consist of four cohorts of healthy male subjects to assess the safety, tolerability and pharmacokinetics of Multiple Ascending Dose (MAD) of CHF6297.

Part 3 will consist of one cohort of COPD patients to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of a repeat dose of CHF6297

Part 4 will consist of one cohort of healthy subjects to assess the anti-inflammatory effect of a repeat dose of CHF6297 after LPS challenge.

Enrollment: 118 patients

Sex: All

Ages: 18 to 75 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

Part 1, Part 2, Part 4 (Healthy subjects):

• Male subjects aged 18-55 years;
• Non smokers
• Lung function above 80% of predicted normal value
• Healthy subjects based on medical evaluation including medical history, physical examination, laboratory tests and cardiac testing
• ability to produce an adequate induced sputum sample (study part 4 only)

Part 3 (COPD patients):

• Males and females aged 40-75 years
• Current or past smokers
• stable patients with a post-bronchodilator FEV1 between 40 and 80% of predicted normal value and FEV1/FVC ratio <0.7
• Ability to produce a spontaneous and an adequate induced sputum sample

Exclusion criteria

Parts 1,2, 4 (Healthy subjects):

• Any clinically relevant abnormalities and/or uncontrolled diseases
• Abnormal laboratory values
• Recent respiratory tract infection
• Hypersensitivity to the drug or excipients
• Positive serology results
• Positive cotinine, alcohol, drug of abuse tests

Part 3 (COPD patients):

• Females of childbearing potential
• History of asthma
• Unstable concomitant diseases
• Abnormal relevant Holter ECG parameters
• Recent acute exacerbations of COPD or respiratory tract infection
• Hypersensitivity to the drug or excipients
• Positive serology results

Trial design

118 participants in 2 patient groups, including a placebo group

CHF6297 Active

Experimental group

Treatment:

Drug: CHF6297 (Part 3)

Drug: CHF6297 (Part 1 - SAD)

Drug: CHF6297 (Part 2 - MAD)

Drug: CHF6297 (Part 4)

Placebo

Placebo Comparator group

Treatment:

Drug: Placebo (Part 4)

Drug: Placebo (Part 1 - SAD)

Drug: Placebo (Part 3)

Drug: Placebo (Part 2 - MAD)