Pharmacodynamics, Pharmacokinetics and Safety of Two Doses of CHF6001 DPI in Subjects With Moderate, Severe COPD

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

61 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-10-31

Study Completion Date

2017-12-28

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Safety, Tolerability and Efficacy of 28-day Inhaled CHF 6001 DPI in COPD Patients

NCT01730404

COPD

COMPLETED PHASE2

Investigate the Safety, Tolerability and Pharmacokinetics of CHF6523 in Healthy and in COPD Subjects

NCT04032535

COPD

COMPLETED PHASE1

Safety and Tolerability of Inhaled CHF 6001 in Healthy Volunteers (HV)

NCT01703052

Chronic Obstructive Pulmonary Disease (COPD)

COMPLETED PHASE1

A Study to Investigate the Safety, Tolerability and Pharmacokinetics of Inhaled CHF6001

NCT02386761

Chronic Obstructive Pulmonary Disease

COMPLETED PHASE1

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

NCT02815488

Chronic Obstructive Pulmonary Disease

TERMINATED PHASE1/PHASE2

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

COPD

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

CHF 6001 Dose1

CHF6001 via NEXThaler® dry powder inhaler (DPI), b.i.d. for 32 consecutive days.

Group Type EXPERIMENTAL

CHF 6001 Dose1

Intervention Type DRUG

CHF 6001 plus placebo

CHF 6001 Dose 2

CHF6001 via NEXThaler® dry powder inhaler (DPI), b.i.d. for 32 consecutive days.

Group Type EXPERIMENTAL

CHF 6001 Dose2

Intervention Type DRUG

CHF 6001 only (high dose)

Placebo

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

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type OTHER

Placebo only

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

CHF 6001 Dose1

CHF 6001 plus placebo

Intervention Type DRUG

CHF 6001 Dose2

CHF 6001 only (high dose)

Intervention Type DRUG

Placebo

Placebo only

Intervention Type OTHER

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

CHF 6001 CHF 6001

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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).

Minimum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No