A Thorough QT (TQT) Study of CHF5993 pMDI in Healthy Volunteers (HV)

Asthma Clinical Trial

Official title:

A Randomized, Double-blind, Positive and Placebo-controlled, Single-dose, Crossover Study of the Effects of CHF5993 pMDI (BDP/FF/GB) at the Proposed Therapeutic and Supratherapeutic Doses, on the Cardiovascular Safety in Healthy Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05830071
• Other study ID #: CLI-05993AB7-03
• Status: Completed
• Phase: Phase 1
• Start date: March 29, 2023
• Est. completion date: October 13, 2023

Study information

• Verified date: October 2023
• Source: Chiesi Farmaceutici S.p.A.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the potential for cardiac repolarization, according to electrocardiographic monitoring (including QT and QTc intervals), of two dose levels of CHF5993 pMDI (beclomethasone dipropionate/formoterol fumarate/glycopyrronium bromide (BDP/FF/GB)) and of one dose of CHF5259 (GB) in healthy subjects compared to moxifloxacin and placebo.

Description:

The main purpose of this study is to evaluate the effect of a single supratherapeutic dose of inhaled BDP/FF/GB on cardiovascular safety. The secondary purposes of the study are to: 1) evaluate the effect of a single supratherapeutic dose of inhaled BDP/FF/GB and GB on cardiovascular safety; 2) establish assay sensitivity by demonstrating the effect of a single oral dose of 400 mg moxifloxacin on cardiovascular safety; 3) determine the pharmacokinetics (PK) of single, inhaled therapeutic and supratherapeutic BDP/FF/GB doses and supratherapeutic GB dose; 4) determine if there is a relationship between the duration of the QTc intervals and the plasma concentrations of the B17MP (beclomethasone 17monopropionate active metabolite of BDP), FF and GB following the administration of BDP/FF/GB and GB pMDIs; 5) generate additional safety and tolerability information.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 95
• Est. completion date: October 13, 2023
• Est. primary completion date: October 13, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Key Inclusion Criteria:

• Subject's written informed consent;

• 18-55 years of age;

• Ability to understand the study procedures, the risks involved and ability to be trained to use the inhalers correctly;

• Body Mass Index (BMI) between 18 and 32 kg/m2 extremes inclusive;

• Non- or ex-smokers who smoked < 5 pack years and stopped smoking > 1 year prior to screening;

• Good physical and mental status, determined on the basis of the medical history and a general clinical examination;

• Vital signs within normal limits at screening and prior to randomization: Diastolic BP 40-89 mmHg, Systolic BP 90-139 mmHg extremes included (mean value of three measures). Body temperature < 37.5°C;

• 12 -lead digitized Electrocardiogram (12-lead ECG) in triplicate considered as normal (40 = Heart rate = 110bpm, 120 ms = PR = 220 ms, QRS = 110 ms, QTcF = 450 ms);

• Lung function measurements within normal limits (normal values: forced expiratory volume in the 1st second [FEV1]/forced vital capacity [FVC] > 0.70 and FEV1 > 80% predicted);

• Female subjects of non-child bearing potential or females of child bearing potential with negative pregnancy test; and acceptable contraceptive methods.

Key Exclusion Criteria:

• Participation in another clinical trial where investigational drug was received and last investigations within the last 8 weeks;

• Clinically significant abnormal standard ECG at screening;

• Clinically relevant and uncontrolled respiratory, cardiac, hepatic, gastrointestinal, renal, endocrine, metabolic, neurologic, or psychiatric disorders that may interfere with successful completion of this protocol;

• Subjects with medical diagnosis of narrow-angle glaucoma, prostatic hypertrophy or bladder neck obstruction that in the opinion of the investigator would prevent use of anticholinergic;

• Subjects with history of breathing problems (i.e., history of asthma including childhood asthma);

• Positive urine test for cotinine;

• Intake of non-permitted concomitant medications in the predefined period prior to screening or prior to randomization, or the subject is expected to take non-permitted concomitant medications during the study;

• Presence of any current infection, or previous infection that resolved less than 7 days prior to screening or to randomization;

• Known intolerance and/or hypersensitivity to any of the excipients contained in the formulation used in the trial;

• Women who are pregnant or lactating;

• Use of any kind of smoking electronic devices within 6 months before Screening.

Other inclusion/exclusion criteria as defined by the protocol.

Related Conditions & MeSH terms

• Asthma
• Chronic Obstructive Pulmonary Disease (COPD)
• Lung Diseases, Obstructive
• Pulmonary Disease, Chronic Obstructive

Intervention

Drug:
• CHF5993
BDP/FF/GB 100/6/12.5 µg pMDI
• CHF5259
GB 12.5 µg pMDI
• Moxifloxacin 400mg
400 mg Oral Tablets
• CHF5993 Placebo
placebo pMDI

Locations

Country	Name	City	State
United States	PAREXEL Baltimore Early Phase Clinical Unit	Baltimore	Maryland

Sponsors (1)

Lead Sponsor	Collaborator
Chiesi Farmaceutici S.p.A.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Effect of BDP/FF/GB pMDI at therapeutic dose on the heart rate-corrected QT interval based on the Fridericia's correction (QTcF).	Placebo-adjusted change in QTc interval based on the Fridericia's correction (??QTcF) after dosing CHF5993 pMDI (200/12/25 µg). Through digitised 12-lead ECG, extracted from 12-Lead Holter ECG.	time 0 (pre-dose) to 24 hours
Secondary	Effect of BDP/FF/GB pMDI and GB pMDI at supra-therapeutic dose on the heart rate-corrected QT interval based on the Fridericia's correction (QTcF).	Placebo-adjusted change from baseline in QTc interval based on the Fridericia's correction (??QTcF) after dosing CHF5993 pMDI (800/48/100 µg) and GB pMDI (100 µg). Through digitised 12-lead ECG, extracted from 12-Lead Holter ECG.	time 0 (pre-dose) to 24 hours
Secondary	Assay sensitivity by demonstrating the effect of a single oral therapeutic dose of moxifloxacin on QTcF.	Placebo-adjusted change from baseline in QTc interval based on the Fridericia's correction (??QTcF) after dosing 400 mg of moxifloxacin. Through digitised 12-lead ECG, extracted from 12-Lead Holter ECG	time 0 (pre-dose) to 6 hours
Secondary	Effect of BDP/FF/GB pMDI at therapeutic and supra-therapeutic dose and of GB pMDI at supra-therapeutic dose on Hearth Rate (HR).	Placebo-adjusted change from baseline of HR (??HR) after dosing BDP/FF/GB pMDI (200/12/25 µg and 800/48/100 µg) and GB pMDI (100 µg) will be summarized by means of descriptive statistics at each analysis time point and by treatment. Through digitised 12-lead ECG, extracted from 12-Lead Holter ECG.	time 0 (pre-dose) to 24 hours
Secondary	Effect of BDP/FF/GB pMDI at therapeutic and supra-therapeutic dose and of GB pMDI at supra-therapeutic dose on PR interval (PR).	Placebo-adjusted change from baseline of PR (??PR) after dosing BDP/FF/GB pMDI (200/12/25 µg and 800/48/100 µg) and GB pMDI (100 µg) will be summarized by means of descriptive statistics at each analysis time point and by treatment. Through digitised 12-lead ECG, extracted from 12-Lead Holter ECG.	time 0 (pre-dose) to 24 hours
Secondary	Effect of BDP/FF/GB pMDI at therapeutic and supra-therapeutic dose and of GB pMDI at supra-therapeutic dose on QRS interval (QRS).	Placebo-adjusted change from baseline of QRS (??QRS) after dosing BDP/FF/GB pMDI (200/12/25 µg and 800/48/100 µg) and GB pMDI (100 µg) will be summarized by means of descriptive statistics at each analysis time point and by treatment. Through digitised 12-lead ECG, extracted from 12-Lead Holter ECG.	time 0 (pre-dose) to 24 hours
Secondary	Effect of BDP/FF/GB pMDI at therapeutic and supra-therapeutic dose and of GB pMDI at supra-therapeutic dose on individual-corrected QT interval (QTcI)	Placebo-adjusted change from baseline in individual-corrected QT interval (??QTcI) after dosing BDP/FF/GB pMDI (200/12/25 µg and 800/48/100 µg) and GB pMDI (100 µg). Through digitised 12-lead ECG, extracted from 12-Lead Holter ECG.	time 0 (pre-dose) to 24 hours
Secondary	Effect of moxifloxacin at therapeutic dose on individual-corrected QT interval.	Placebo-adjusted change from baseline in individual-corrected QT interval (??QTcI) after dosing 400 mg of moxifloxacin. Through digitised 12-lead ECG, extracted from 12-Lead Holter ECG.	time 0 (pre-dose) to 6 hours
Secondary	Changes in T-wave morphology and U-wave presence.	Frequency of treatment-emergent changes in T-wave morphology and U-wave presence after dosing BDP/FF/GB pMDI (200/12/25 µg and 800/48/100 µg) and GB pMDI (100 µg). Through digitised 12-lead ECG, extracted from 12-Lead Holter ECG.	time 0 (pre-dose) to 24 hours
Secondary	Analysis of categorical outliers of Hearth Rate (HR), PR interval (PR), QRS interval (QRS) and QTcF interval (QTcF), after BDP/FF/GB pMDI dosing at therapeutic and supra-therapeutic dose, and after GB dosing at supra-therapeutic dose.	Results of categorical outliers will be summarized by treatment in frequency tables reporting: counts and percentages for number of subjects and number of time points with 1) abnormal actual QTcF values, and 2) abnormal change from baseline of HR, PR, QRS and QTcF. Through digitised 12-lead ECG, extracted from 12-Lead Holter ECG.	time 0 (pre-dose) to 24 hours
Secondary	Analysis of Maximum plasma concentration (Cmax), pharmacokinetic parameter of FF, GB, BDP and B17MP	Analysis of Cmax after dosing BDP/FF/GB pMDI (200/12/25 µg and 800/48/100 µg) and GB pMDI (100 µg).	time 0 (pre-dose) to 24 hours
Secondary	Analysis of Area under the curve from 0 to 12 hours post-dose (AUC0-12), pharmacokinetic parameter of FF, GB, BDP and B17MP	Analysis of AUC0-12, after dosing BDP/FF/GB pMDI (200/12/25 µg and 800/48/100 µg) and GB pMDI (100 µg).	time 0 (pre-dose) to 24 hours
Secondary	Analysis of Area under the plasma concentration-time curve from time 0 to time t (AUC0 t), pharmacokinetic parameter of FF, GB, BDP and B17MP	Analysis of AUC0-t after dosing BDP/FF/GB pMDI (200/12/25 µg and 800/48/100 µg) and GB pMDI (100 µg).	time 0 (pre-dose) to 24 hours
Secondary	Analysis of Area under the curve from time 0 to infinity (AUC0-8), pharmacokinetic parameter of FF, GB, BDP and B17MP	Analysis of AUC0-8 after dosing BDP/FF/GB pMDI (200/12/25 µg and 800/48/100 µg) and GB pMDI (100 µg).	time 0 (pre-dose) to 24 hours
Secondary	Analysis of Time to maximum plasma concentration (tmax), pharmacokinetic parameter of FF, GB, BDP and B17MP	Analysis of tmax, after dosing BDP/FF/GB pMDI (200/12/25 µg and 800/48/100 µg) and GB pMDI (100 µg).	time 0 (pre-dose) to 24 hours
Secondary	Analysis of Terminal half-life (t1/2), pharmacokinetic parameter of FF, GB, BDP and B17MP	Analysis of t1/2, after dosing BDP/FF/GB pMDI (200/12/25 µg and 800/48/100 µg) and GB pMDI (100 µg).	time 0 (pre-dose) to 24 hours
Secondary	Incidence of Adverse events	Number and percentage of subjects with at least one event and number of treatment emergent events	from study start through study completion, an average of 4 months
Secondary	Incidence of Adverse Drug Reactions	Number and percentage of subjects with at least one event and number of treatment emergent events	from study start through study completion, an average of 4 months
Secondary	Change of systolic and diastolic blood pressure	Number and percentage of subjects with with abnormal changes from baseline	from study start through study completion, an average of 4 months
Secondary	Body temperature abnormal values	Number and percentage of subjects with at least one event and number of treatment emergent events	from study start through study completion, an average of 4 months
Secondary	Abnormal results of physical examinations	Number and percentage of subjects with at least one event and number of treatment emergent events	from study start through study completion, an average of 4 months
Secondary	Abnormal clinical chemistry and haematology laboratory tests	Number and percentage of subjects with at least one event and number of treatment emergent events	from study start through study completion, an average of 4 months