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PK of BDP/FF/GB Single-inhaler Triple Therapy in Japanese vs. Caucasians

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ClinicalTrials.gov Identifier: NCT03859414
Recruitment Status : Recruiting
First Posted : March 1, 2019
Last Update Posted : March 21, 2019
Sponsor:
Information provided by (Responsible Party):
Chiesi Farmaceutici S.p.A.

Brief Summary:
The purpose of conducting this study is to obtain PK data of Beclometasone Dipropionate (BDP)/Beclometasone-17-MonoPropionate (B17MP), Formoterol Fumarate (FF) and Glycopyrronium Bromide (GB) after inhalation of CHF 5993 in Japanese as well as Caucasian healthy subjects under the same setting.

Condition or disease Intervention/treatment Phase
Asthma Chronic Obstructive Pulmonary Disease Drug: Therapeutic Dose 1 Drug: Therapeutic Dose 2 Drug: Supra-therapeutic Dose Drug: Placebo Phase 1

Detailed Description:

The Study is single-centre, randomized, double-blind, single-dose, 4-way cross-over, placebo-controlled.

The safety, tolerability, PD and PK of CHF 5993 will be assessed in Japanese and Caucasian healthy volunteers.

A total of 32 healthy male and female volunteers are planned to be included where they will receive four different treatments (study drug or placebo) over four treatment periods.

Standard safety assessments will be conducted during the study, including safety blood and urine laboratory tests, liver function tests, vital signs, physical examinations, ECGs, 24-hour Holter and observations of any adverse events. Blood samples will also be collected for PK analysis. Blood and urine samples will be collected for pharmacodynamics analysis.


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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 32 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Intervention Model Description: 4-way Crossover Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Other
Official Title: A Single-center, Randomized, Double-blind, Single Dose, 4-way Cross-over, Placebo-controlled Ethnic Sensitivity Study to Assess the Pharmacokinetics (PK), Pharmacodynamics (PD), Safety, and Tolerability of Different Dosages of CHF 5993 Pressurized Metered Dose Inhaler (pMDI) in Caucasian and Japanese Healthy Subjects
Actual Study Start Date : March 18, 2019
Estimated Primary Completion Date : November 2019
Estimated Study Completion Date : November 2019

Arm Intervention/treatment
Active Comparator: Therapeutic Dose 1
Single dose administration of CHF 5993 100/6/12.5 µg pMDI 2 inhalations. Total dose of CHF 5993 pMDI = 200/12/25 µg
Drug: Therapeutic Dose 1
CHF 5993 100/6/12.5 µg pMDI, fixed combination of BDP 100 µg + FF 6 µg + GB 12.5 µg.

Active Comparator: Therapeutic Dose 2
Single dose administration of CHF 5993 200/6/12.5 µg pMDI 2 inhalations. Total dose of CHF 5993 pMDI = 400/12/25 µg
Drug: Therapeutic Dose 2
CHF 5993 200/6/12.5 µg pMDI, fixed combination of BDP 200 µg + FF 6 µg + GB 12.5 µg.

Active Comparator: Supra-therapeutic Dose
Single dose administration of CHF 5993 100/6/12.5 µg pMDI 8 inhalations Total dose of CHF 5993 pMDI = 800/48/100 µg
Drug: Supra-therapeutic Dose
CHF 5993 200/6/12.5 µg pMDI, fixed combination of BDP 200 µg + FF 6 µg + GB 12.5 µg.

Placebo Comparator: Placebo
Single dose administration of CHF 5993 pMDI placebo
Drug: Placebo
CHF 5993 placebo pMDI




Primary Outcome Measures :
  1. Area Under the Curve (AUC) of B17MP, formoterol and GB [ Time Frame: Over 24 hours after administration for B17MP and FF, over 48 hours after administration for GB ]
    Area under the plasma concentration versus time curve after a single-dose administration of CHF 5993 pMDI

  2. Maximum of Concentration (Cmax) of B17MP, FF and GB [ Time Frame: Over 24 hours after administration for B17MP and FF, over 48 hours after administration for GB ]
    Peak Plasma Concentration after a single-dose administration of CHF 5993 pMDI


Secondary Outcome Measures :
  1. Number of Adverse Events (AEs) [ Time Frame: through study completion, an average of 13 weeks ]
    Assessment of the general safety and tolerability in terms of number of Treatment Emergent Adverse Event (TEAEs), Adverse Drug Reaction (ADRs), serious TEAEs, severe TEAEs and TEAEs leading to study discontinuation and to death.

  2. Number of subjects with Adverse Events [ Time Frame: through study completion, an average of 13 weeks ]
    Assessment of the general safety and tolerability in terms number of subjects with TEAEs, ADRs, serious TEAEs, severe TEAEs and TEAEs leading to study discontinuation and to death.

  3. Percentage of subjects with Adverse Events [ Time Frame: through study completion, an average of 13 weeks ]
    Assessment of the general safety and tolerability in terms of incidence of TEAEs, ADRs, serious TEAEs, severe TEAEs and TEAEs leading to study discontinuation and to death.

  4. Clinical laboratory parameters (biochemistry) [ Time Frame: Over 24 hours after administration ]
    Assessment of PD profile in terms of plasma cortisol, serum potassium and serum glucose after a single-dose administration of CHF 5993 pMDI

  5. Clinical laboratory parameters (urinalysis) [ Time Frame: Over 24 hours after administration ]
    Assessment of PD profile in terms of urine cortisol and creatinine excretion after a single-dose administration of CHF 5993 pMDI

  6. Heart rate [ Time Frame: Over 24 hours after administration ]
    Assessment of PD profile in terms of the Heart Rate after a single-dose administration of CHF 5993 pMDI

  7. 12-lead ECG parameters [ Time Frame: Over 24 hours after administration ]
    Assessment of pharmacodynamics profile in terms of 12-lead ECG parameters extracted from Holter after a single-dose administration of CHF 5993 pMDI

  8. Vital signs [ Time Frame: Over 24 hours after administration ]
    Assessment of pharmacodynamics profile in terms of vital signs (systolic and diastolic blood pressure) after a single-dose administration of CHF 5993 pMDI



Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years to 55 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Subject's written informed consent obtained prior to any study related procedure;
  • Healthy male and female subjects aged 20 to 55 years inclusive;
  • For Japanese subjects: must be a Japanese subject who has resided outside Japan for no more than 5 years, born in Japan and holding a Japanese passport, with all 4 grandparents Japanese, as confirmed by interview;
  • Subject must be willing and able to adhere to the prohibitions and restrictions specified in this protocol and to comply with the correct use of the devices specified in this protocol;
  • Body mass index within the range of 18.0 to 25.0 kg/m2 inclusive;
  • Non-smokers or ex-smokers who smoked <5 pack years and stopped smoking >1 year prior to screening;
  • Subject must be healthy on the basis of physical examination, medical history, vital signs, and 12 -lead digitised Electrocardiogram (12-lead ECG);
  • Vital signs (Blood pressure and body temperature) within normal limits;
  • 12-lead ECG considered as normal;
  • Lung function measurements within normal limits;
  • Women of non-childbearing potential (WONCBP) and women of childbearing potential (WOCBP) fulfilling one of the following criteria: a) WOCBP with fertile male partners: they and/or their partner must be willing to use a highly effective birth control method from the signature of the informed consent and until the follow-up visit or b) WOCBP with non-fertile male partners: (contraception is not required in this case).
  • Female subject, except if postmenopausal, must have a negative serum beta-human chorionic gonadotropin at screening and a negative urine pregnancy test at Day -1 prior the first drug administration;
  • Subjects must agree not to donate sperm or ova from the time of the first administration of study medication until three months after the end of the systemic exposure of the study drug or until the last follow-up visit, whichever occurs later;
  • Males fulfilling one of the following criteria: a) Males with pregnant or non-pregnant WOCBP partners: they must be willing to use male condom from the signature of the informed consent and until the follow-up visit or b) Non-fertile male subjects (contraception is not required in this case) or c) Males with partner not of childbearing potential (contraception is not required in this case).

Exclusion Criteria:

  • Participation in another clinical trial with an investigational drug in the 90 days or 5 half-lives of non-biological entities of that investigational drug (whichever is longer) preceding the administration of the study drug;
  • Clinically relevant and uncontrolled respiratory, cardiac, hepatic, gastrointestinal, renal, endocrine, metabolic, neurologic, or psychiatric disorders that may interfere with successful completion of this study;
  • Any other abnormal findings on vital signs, ECG, physical examination or laboratory evaluation of blood and urine samples that the investigator judges as likely to interfere with the study or pose an additional risk in participating;
  • Medical diagnosis of narrow-angle glaucoma, prostatic hypertrophy or bladder neck obstruction that in the opinion of the investigator would prevent use of anticholinergic;
  • History of asthma, including childhood asthma, Chronic Obstructive Pulmonary Disease (COPD) or any other chronic pulmonary diseases or condition;
  • Positive HIV1 or HIV2 serology;
  • results from the Hepatitis serology at screening which indicates acute or chronic Hepatitis (i.e. positive HB surface antigen (HBsAg), HB core antibody (anti-HBc), or Hepatitis C (positive HCV antibody);
  • Blood donation or blood loss (equal or more than 450 mL), less than 2 months prior to randomisation;
  • Abnormal haemoglobin level defined as <12.0 g/dL in females and <14.0 g/dL in males;
  • Positive urine test for cotinine at screening or prior to randomisation;
  • Unsuitable veins for repeated venepuncture;
  • History or clinical evidence of drug and/or alcohol abuse within 12 months prior to screening and randomisation;
  • Known intolerance/hypersensitivity to any of the excipients/components contained in any of the formulations used in the trial;
  • Taking any drug treatment, including prescribed or Over the Counter (OTC) medicines as well as homeopathic remedies etc., in the 14 days before the screening and prior randomisation, with the exception of occasional paracetamol (maximum 3 g per day with a maximum of 10 g per 14 days for mild non-exclusionary conditions), hormonal contraceptives; hormonal replacement treatment for post-menopausal women, occasional ibuprofen (maximum 1.2 g per day, not to exceed 12 g in the 14 days before the screening);
  • Taking enzyme-inducing drugs, enzyme-inhibiting drugs, biologic drugs or any drug known to have a well-defined potential for hepatotoxicity (e.g. isoniazide, nimesulide, ketoconazole) in the 3 months before screening or prior to randomisation;
  • Heavy caffeine drinker >28 cups/week of coffee or similar caffeinated beverages e.g., tea, cola per day);
  • Bacterial or viral respiratory tract, sinus or middle ear infection affecting health status within 4 weeks prior to randomisation;
  • Night shift workers with night shifts within 8 weeks prior to randomisation and during the study.

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): NCT03859414


Contacts
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Contact: Chiesi Clinical Trial Info +39 0521 2791 clinicaltrials_info@chiesi.com

Locations
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United Kingdom
Richmond Pharmacology Ltd Recruiting
London, Tooting, United Kingdom, SW17 0RE
Contact: Lihn Schram    +44 (0)20 7042 5800    l.schram@richmondpharmacology.com   
Principal Investigator: Jorg Taubel, MD         
Sponsors and Collaborators
Chiesi Farmaceutici S.p.A.

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Responsible Party: Chiesi Farmaceutici S.p.A.
ClinicalTrials.gov Identifier: NCT03859414     History of Changes
Other Study ID Numbers: CLI-05993AB4-01
First Posted: March 1, 2019    Key Record Dates
Last Update Posted: March 21, 2019
Last Verified: March 2019

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
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Lung Diseases
Lung Diseases, Obstructive
Pulmonary Disease, Chronic Obstructive
Respiratory Tract Diseases