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| ID | Type | Description | Link |
|---|---|---|---|
| 2015-003075-30 | EudraCT Number |
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Very poor recruitment in the Part 4 of the study
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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| CHF6297 Active | Experimental |
| |
| Placebo | Placebo Comparator |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| CHF6297 (Part 1 - SAD) | Drug | Single doses of CHF6297 at each period (for up to 3 periods per subject) |
|
| Measure | Description | Time Frame |
|---|---|---|
| Adverse events | Treatment-related Adverse events | Part 1 from Day 1 until Day 4, Part 2 from Day 1 until Day 8, Part 3 from Day 1 until Day 17, Part 4 from Day 1 until Day 8 |
| Change in Vital signs | Blood pressure | Part 1 from Day 1 until Day 4, Part 2 from Day 1 until Day 8, Part 3 from Day 1 until Day 17 |
| Change in Holter ECG parameters | HR, QTcF, PR, QRS + holter recording abnormalities | Part 1 Day 1-2, Part 2 Day 1-2 and Day 7-8, Part 3 Day 1-2 and Day 14-15 |
| Change in FEV1 | Forced exhalation volume in the first second | Part 1 Day 1-2, Part 2 Day 1 and Day 7-8, Part 3 Day 1, Day 10 and Day 14 |
| Change in Laboratory parameters | Clinical chemistry and haematology + urinalysis | Part 1 Day 1 and Day 4, Part 2 Day 1 and Day 8, Part 3 Day 1 and Day 15 |
| Measure | Description | Time Frame |
|---|---|---|
| Area under the plasma concentration vs time curve | Part 1 Day 1 until Day 4, Part 2 Day 1 and Day 7, Part 3 Day 1 and Day 14 | |
| Peak plasma concentration (Cmax) | maximum plasma concentration of CHF6297 |
| Measure | Description | Time Frame |
|---|---|---|
| Part 3: markers of inflammation (exploratory) | Blood and sputum biomarkers | after 14 days of dosing |
| Part 4: markers of inflammation (exploratory) | Blood and sputum biomarkers |
Inclusion criteria:
Part 1, Part 2, Part 4 (Healthy subjects):
Part 3 (COPD patients):
Exclusion Criteria:
Parts 1,2, 4 (Healthy subjects):
Part 3 (COPD patients):
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| Name | Affiliation | Role |
|---|---|---|
| Stuart Mair, MD | Quotient Clinical | Principal Investigator |
| Dave Singh, MD | Medicines Evaluation Unit | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Quotient Clinical | Ruddington | Nottingham | NG11 6JS | United Kingdom | ||
| Medicines Evaluation Unit |
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| Label | URL |
|---|---|
| Study Record on EU Clinical Trials Register including results | View source |
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| Placebo (Part 1 - SAD) | Drug | Single doses of placebo matching CHF6297 at each period (for up to 3 periods per subject) |
|
| CHF6297 (Part 2 - MAD) | Drug | Twice daily doses of CHF6297 for 7 days |
|
| Placebo (Part 2 - MAD) | Drug | Twice daily doses of placebo matching CHF6297 for 7 days |
|
| CHF6297 (Part 3) | Drug | Twice daily doses of CHF6297 for 14 days |
|
| Placebo (Part 3) | Drug | Twice daily doses of placebo matching CHF6297 for 14 days |
|
| CHF6297 (Part 4) | Drug | Twice daily doses of CHF6297 for 7 days |
|
| Placebo (Part 4) | Drug | Twice daily doses of placebo matching CHF6297 for 7 days |
|
| Part 1 Day 1 until Day 4, Part 2 Day 1 and Day 7, Part 3 Day 1 and Day 14 |
| Time to reach the maximum plasma concentration (tmax) | Part 1 Day 1 until Day 4, Part 2 Day 1 and Day 7, Part 3 Day 1 and Day 14 |
| Elimination half-life (t1/2) | Part 1 Day 1 until Day 4, Part 2 Day 1 and Day 7, Part 3 Day 1 and Day 14 |
| Clearance (CL/F) | Absolute plasma clearance | Part 1 Day 1 until Day 4, Part 2 Day 1 and Day 7, Part 3 Day 1 and Day 14 |
| Volume of distribution (Vz/F) | plasma volume of distribution | Part 1 Day 1 until Day 4, Part 2 Day 1 and Day 7, Part 3 Day 1 and Day 14 |
| Urinary excretion (Ae) | Amount of CHF6297 excreted in urine | Part 1 from Day 1 to Day 4, Part 2 Day 1 and Day 7 |
| fraction excreted (fe) | Percentage of drug excreted in urine | Part 1 from Day 1 to Day 4, Part 2 Day 1 and Day 7 |
| Renal clearance (CLr) | Part 1 from Day 1 to Day 4, Part 2 Day 1 and Day 7 |
| after 7 days of dosing |
| Manchester |
| M23 9QZ |
| United Kingdom |
| ID | Term |
|---|---|
| D029424 | Pulmonary Disease, Chronic Obstructive |
| ID | Term |
|---|---|
| D008173 | Lung Diseases, Obstructive |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D002908 | Chronic Disease |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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