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Trial record 1 of 1 for:    NCT03004417
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Pharmacodynamics, Pharmacokinetics and Safety of Two Doses of CHF6001 DPI in Subjects With Moderate, Severe COPD

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ClinicalTrials.gov Identifier: NCT03004417
Recruitment Status : Completed
First Posted : December 28, 2016
Last Update Posted : February 18, 2019
Sponsor:
Collaborator:
SGS S.A.
Information provided by (Responsible Party):
Chiesi Farmaceutici S.p.A.

Brief Summary:
Effect of CHF 6001 on biomarkers of inflammation in induced sputum and in blood, on pulmonary function and on symptoms benefits in comparison with placebo.

Condition or disease Intervention/treatment Phase
COPD Drug: CHF 6001 Dose1 Drug: CHF 6001 Dose2 Other: Placebo Phase 2

Detailed Description:
The purpose of this study is to obtain information on the effects of two doses of CHF6001 on sputum and blood biomarkers of inflammation in subjects with symptomatic COPD with moderate, severe airflow limitation and with chronic bronchitis. The efficacy of the treatment will also be measured using forced oscillometry technique and spirometry. Safety, tolerability and pharmacokinetics will be evaluated.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 61 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: A Randomised, Double-blind,Placebo Controlled, Repeated Dose, Three-way Crossover Study to Evaluate the Pharmacodynamics, Pharmacokinetics and Safety of Two Doses of CHF6001 DPI in Subjects With Moderate, Severe COPD
Actual Study Start Date : October 31, 2016
Actual Primary Completion Date : December 28, 2017
Actual Study Completion Date : December 28, 2017

Arm Intervention/treatment
Experimental: CHF 6001 Dose1
CHF6001 via NEXThaler® dry powder inhaler (DPI), b.i.d. for 32 consecutive days.
Drug: CHF 6001 Dose1
CHF 6001 plus placebo
Other Name: CHF 6001

Experimental: CHF 6001 Dose 2
CHF6001 via NEXThaler® dry powder inhaler (DPI), b.i.d. for 32 consecutive days.
Drug: CHF 6001 Dose2
CHF 6001 only (high dose)
Other Name: CHF 6001

Placebo Comparator: Placebo
Matching placebo via NEXThaler® dry powder inhaler (DPI), b.i.d. for 32 consecutive days.
Other: Placebo
Placebo only




Primary Outcome Measures :
  1. Sputum biomarkers [ Time Frame: Change from baseline to end of treatment (mean Day 20, 26 and 32 values) at each period; ]
    - IL-6, IL-8 (CXCL-8), IL-1β, TNF-α, MIP1β, MCP-1, MyeloPerOxidase (MPO), Neutrophil Elastase (NE), MMP9, Acetyl-proline-glycine-proline (AcPGP), leukotriene B4 (LTB4), eosinophil cationic protein (ECP) and α2‐macroglobulin.

  2. Sputum biomarkers [ Time Frame: Predose and end of treatment at Day 32 of each period ]
    Sputum gene expression analysis

  3. Sputum cell count [ Time Frame: Change from baseline to end of treatment (mean Day 20, 26 and 32 values) at each period; ]
    • Total cell count
    • Absolute and percent of neutrophils, eosinophils, macrophages and lymphocytes differential cell count.

  4. Blood Biomarkers [ Time Frame: Change from baseline to Day 32 of each period; ]
    Blood Biomarkers

  5. Blood Biomarkers [ Time Frame: Predose and end of treatment at Day 32 of each period ]
    Blood gene expression analysis

  6. Lung function: Spirometry [ Time Frame: Change from baseline to Day 20 Day 26 and 32 of each period ]
    pre-dose FEV1, FVC and IC

  7. Lung function: Oscillometry [ Time Frame: Change from baseline to Day 32 of each period ]
    R5, R19, R5-R19, X5, EFL index

  8. PK: AUC0-12h,ss [ Time Frame: on Day 32 (steady state) of each period. ]
  9. PK: Cmax [ Time Frame: on Day 32 (steady state) of each period. ]


Information from the National Library of Medicine

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Ages Eligible for Study:   40 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Male and female aged ≥40 years
  • A female is eligible to enter the study if she is of non-childbearing potential i.e. physiologically incapable of becoming pregnant Women physiologically capable of becoming pregnant (i.e. women of childbearing potential) are eligible to enter the study if they have negative pregnancy test at screening and agree to use one or more of the following highly effective contraceptive measures
  • Subjects with an established diagnosis of COPD (according to GOLD guidelines, update 2015) at least 12 months prior to the screening visit
  • With a smoking history of at least 10 pack-years [pack-years=number of cigarettes per day x number of years/20]. Current and ex- smokers are eligible. With a BMI in the range of 18-35 Kg/m2 With a post-bronchodilator FEV1 ≥30% and ≤70%
  • Subjects must be receiving daily maintenance with triple therapy (ICS plus LABA plus LAMA) at stable dose and dosing regimen, for at least 2 months prior to screening
  • With a history of chronic bronchitis defined as chronic cough and sputum production for more than three months per year for two or more years and known as 'spontaneous sputum producer' subject
  • Subjects must be symptomatic at screening defined as having a CAT score ≥10
  • Subjects must be able to be trained to correctly use the DPI inhalers and They must have a cooperative attitude and ability to perform the required outcome measurements (e.g. spirometry testing, induced sputum...).

Exclusion Criteria:

  • Pregnant or lactating female subject
  • Subjects with a current diagnosis of asthma
  • Subjects with a moderate or severe COPD exacerbation [i.e. resulting in the use of systemic (oral/IV/IM corticosteroids) and/or antibiotics or in hospitalisation] or a lower respiratory tract infection within 6 weeks prior to study entry or during the screening period
  • Subjects on maintenance bronchodilators therapy only (LABA alone, LAMA alone, dual LABA/LAMA alone) or maintenance dual therapy only (ICS/LABA or ICS plus LAMA) within 2 months prior to study entry
  • Subjects on PDE4 inhibitors (e.g. roflumilast) within 2 months prior to study entry
  • Subjects requiring long-term (at least 12 hours daily) oxygen therapy for chronic hypoxemia; participating to a pulmonary rehabilitation programme or completing such a programme within the last 6 weeks prior to study entry
  • Subjects with known respiratory disorders other than COPD...
  • Subjects have lung cancer or a history of lung cancer or with active cancer or a history of cancer (other than lung) with less than 5 years disease free survival time
  • Subjects with a known history of hypersensitivity to beta2-agonist, PDE4 inhibitors or any of the excipients contained in any of the formulations used in the trial
  • Subjects with a diagnosis of depression associated with suicidal ideation or behaviour or with a diagnosis of generalised anxiety disorder that in the investigator's opinion would place the patient at risk
  • Subjects who have known history of clinically significant cardiovascular conditions such as, but not limited to, unstable or acute ischemic heart disease within one year prior to study entry, NYHA Class III/IV heart failure, known history of sustained and non-sustained cardiac arrhythmias or history of atrial fibrillation diagnosed in the last 6 months prior to study entry and not controlled with therapy rate control strategy
  • Subjects who have unstable concurrent disease
  • Subjects with clinically significant laboratory abnormalities
  • Current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones)
  • Subjects receiving treatment with any drug known to have a well-defined potential for hepatotoxicity (e.g. isoniazide, nimesulide, ketoconazole) within the previous 3 months prior to the study entry and during the screening period
  • Subjects have experienced excessive weight loss recently (which cannot be explained by the natural course of COPD or known background conditions).
  • Subjects with a history of alcohol abuse and/or substance/drug abuse within 12 months prior to screening visit
  • Subjects having received any other investigational drug within the preceding 30 days (60 days for biologics).

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03004417


Locations
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United Kingdom
Medicines Evaluation Unit Ltd
Manchester, United Kingdom, M23 9QZ
Sponsors and Collaborators
Chiesi Farmaceutici S.p.A.
SGS S.A.
Investigators
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Principal Investigator: Dave Singh, MD MEU - Manchester - UK

Additional Information:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Chiesi Farmaceutici S.p.A.
ClinicalTrials.gov Identifier: NCT03004417     History of Changes
Other Study ID Numbers: CCD-06001AA1-10
2015-005550-35 ( EudraCT Number )
First Posted: December 28, 2016    Key Record Dates
Last Update Posted: February 18, 2019
Last Verified: February 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No