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Clinical Pharmacology Study to Evaluate the Total Systemic Exposure and Lung Bioavailability of CHF 5993 pMDI Combination in Healthy Volunteers

30. Juni 2021 aktualisiert von: Chiesi Farmaceutici S.p.A.

Cross-over Clinical Pharmacology Study, to Evaluate the Total Systemic Exposure and Lung Bioavailability of CHF 5993 pMDI Combination Across Two Different Dose Strengths, Administered With and Without Activated Charcoal, in Healthy Volunteers

The study is performed to evaluate the total systemic exposure and lung bioavailability of CHF 5993 pMDI combination, in healthy volunteers subjects.

Studienübersicht

Studientyp

Interventionell

Einschreibung (Tatsächlich)

50

Phase

  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

      • Antwerpen, Belgien
        • SGS CPU Antwerpen

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre bis 55 Jahre (Erwachsene)

Akzeptiert gesunde Freiwillige

Ja

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  1. Subject's written informed consent obtained prior to any study related procedure.
  2. Able to understand the study procedures, the risks involved and ability to be trained to use the devices correctly.
  3. Male and female subjects aged 18 to 55 years inclusive.
  4. Body mass index (BMI) within the range of 18 to 30 kg/m2 inclusive.
  5. Non- or ex-smokers who smoked < 5 pack years (pack-years = the number of cigarette packs per day, times the number of years) and stopped smoking > 1 year prior to screening.
  6. Good physical and mental status, determined on the basis of the medical history and a general clinical examination, at screening and before randomization.
  7. Lung function measurements within normal limits (Normal values (according to GINA 2014 document): FEV1/FVC > 0.70 and FEV1 > 80% predicted).
  8. Male subjects: they and/or their partner must be willing to use an approved method of contraception from the time of screening and until 30 days after the last dose of study. Subjects must not donate sperm for 30 days after the last dose of study drug.*
  9. Female subjects: post-menopausal women having at least 12 months of natural (spontaneous) amenorrhea, or women of childbearing potential (defined as all women physiologically capable of becoming pregnant), using an acceptable method of contraception
  10. Surgical sterilization (i.e. bilateral tubal ligation, hysterectomy for females; vasectomy for males)
  11. Hormonal contraception (implantable, injectable, patch, oral)
  12. Double-barrier methods: condom and occlusive cap (diaphragm or cervical/vault caps)
  13. Placement of an intrauterine device (IUD) or intrauterine system (IUS).

Exclusion Criteria:

  1. Blood donation (equal or more than 450 ml) or blood loss, less than 8 weeks before inhalation of the study medication.
  2. Female subjects: pregnant or lactating women (where pregnancy is defined as the state of a female after conception and until the termination of the gestation) confirmed by a positive urine test at screening and randomization.
  3. Positive HIV1 or HIV2 serology.
  4. Positive results from the Hepatitis serology which indicates acute or chronic Hepatitis B or Hepatitis C.
  5. Unsuitable veins for repeated venipuncture.
  6. History of alcohol abuse within 12 months prior to screening.
  7. History of drug abuse within 12 months prior to screening (or positive urine drug test performed at screening).
  8. Subjects who have a positive urine test for cotinine.
  9. Clinically relevant abnormal laboratory values suggesting an unknown disease and requiring further clinical investigation. Note: In case of abnormal laboratory values, the test can be performed again once before randomization.
  10. Clinically relevant and uncontrolled hepatic, gastrointestinal, endocrine, metabolic, neurologic, or psychiatric disorder that may interfere with successful completion of this protocol.
  11. History of glaucoma, symptomatic prostatism or urinary retention.
  12. Subjects who have cardiovascular condition such as, but not limited to, unstable ischemic heart disease, NYHA Class III/IV left ventricular failure, acute ischemic heart disease in the last year prior to study screening, history of sustained cardiac arrhythmias or sustained and non-sustained cardiac arrhythmias diagnosed in the last 6 months (sustained means lasting more than 30 seconds and or ending only with external action, and or leads to hemodynamic collapse; non-sustained means > 3 beats < 30 seconds, and or ending spontaneously, and or asymptomatic), impulse conduction high degree blocks, ICD implant
  13. Abnormal ECG (i.e.: QRS > 120 msec, PR > 220 msec, HR < 40 bpm, HR > 110 bpm, QTcF > 450 ms for males or QTcF > 470 ms for females) at screening.

    Note: In case of abnormal ECG, the test can be performed again once before randomization.

  14. Clinically significant abnormal 24h-Holter monitoring at screening (if necessary the Holter evaluation can be done on another day before randomization).
  15. Abnormal Blood Pressure (Average Diastolic Blood Pressure > 90 mmHg or average Systolic Blood Pressure > 140 mmHg) at screening.

    Note: In case of abnormal blood pressure, measure can be done again once before randomization.

  16. Participation in another clinical trial where investigation drug was received less than 8 weeks prior to screening.
  17. History of hypersensitivity to any of the excipients contained in the formulations used in the trial.
  18. Subject taking any drug treatment, including prescribed or OTC medicines as well as vitamins, homeopathic remedies etc, taken in the 14 days before the screening with the exception of :

    1. Occasional paracetamol (maximum 2 g per day with a maximum of 10 g per 14 days for mild non-excluding conditions);
    2. Hormonal contraceptives;
    3. Hormonal replacement treatment for post-menopausal women.
  19. Subject taking treatment, with enzyme-inducing or enzyme-inhibiting drugs and biologic drugs and with any drug known to have a well-defined potential for hepatotoxicity (e.g. isoniazide, nimesulide, ketoconazole), taken since 3 months before screening until randomization.
  20. Heavy caffeine drinker (> 5 caffeinated beverages e.g., coffee, tea, cola per day).

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Crossover-Aufgabe
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: CHF 5993 HS 200/6/25 pMDI
High Strength fixed combination
Aktiver Komparator: CHF 5993 MS 100/6/25 pMDI
Medium Strength fixed combination
Experimental: CHF 5993 HS 200/6/25 pMDI + Charcoal Block
High Strength fixed combination plus Charcoal Block
Aktiver Komparator: CHF 5993 MS 100/6/25 pMDI + Charcoal Block
Medium Strength fixed combination plus Charcoal Block
Placebo-Komparator: Placebo pMDI
Placebo

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Systemic exposure of B17MP, Formoterol and Glycopyrronium bromide, without charcoal block (To evaluate the total systemic exposure as AUCt and Cmax) Composite outcome measures of PK variables
Zeitfenster: over 32hours after administration
Composite outcome measures of PK variables
over 32hours after administration
Lung exposure of B17MP, Formoterol and Glycopyrronium bromide without charcoal block (To evaluate the lung exposure (as AUCt and Cmax) Composite outcome measures of PK variables
Zeitfenster: over 32hours after administration
Composite outcome measures of PK variables
over 32hours after administration

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Systemic effects of CHF5993 (To evaluate the systemic effects as potassium and glucose levels) Composite outcome measures of PD variables
Zeitfenster: over 24hours after administration
Composite outcome measures of PD variables
over 24hours after administration
Systemic cardiac effects and the general safety (Composite outcome measures of cardiac variables (such as HR, BP, QT) and safety variables (such as AE, SAE)
Zeitfenster: over 24hours after administration
Composite outcome measures of cardiac variables (such as HR, BP, QT) and safety variables (such as AE, SAE)
over 24hours after administration

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. Februar 2015

Primärer Abschluss (Tatsächlich)

1. April 2015

Studienabschluss (Tatsächlich)

1. Juli 2015

Studienanmeldedaten

Zuerst eingereicht

30. Januar 2015

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

9. Februar 2015

Zuerst gepostet (Schätzen)

10. Februar 2015

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

2. Juli 2021

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

30. Juni 2021

Zuletzt verifiziert

1. Juni 2021

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • CCD-05993AB2-01

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

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Klinische Studien zur CHF 5993 HS 200/6/25 pMDI

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