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A Study to Assess the Pharmacokinetics (PK), Pharmacodynamics (PD) and Safety of 2-Week Treatment With Inhaled AZD7594 in Adolescents (12 to 17 Years) With Asthma

27. januar 2021 oppdatert av: AstraZeneca

An Open-Label, Multi-Centre, Phase I Study to Assess the Pharmacokinetics, Pharmacodynamics and Safety of 2-Week Treatment With Inhaled AZD7594 in Adolescents (12 to 17 Years) With Asthma

This is an open-label, multi-centre, Phase I study to assess the PK, PD and safety of 2 week treatment with inhaled AZD7594 in adolescent patients with asthma.

The study is planned to be conducted at 4-10 study sites in the United States. The study intends to include 24 patients (12 to 17-year-old patients). For each patient, the duration of participation in the study will be approximately 5 to 7 weeks (37 to 52 days).

Studieoversikt

Status

Fullført

Forhold

Intervensjon / Behandling

Detaljert beskrivelse

This is an open-label, multi-centre, Phase I study to assess the PK, PD and safety of 2 week treatment with inhaled AZD7594 in adolescent patients with asthma.

The study is planned to be conducted at 4-10 study sites in the United States. Eligible 12 to 17-year-old patients with asthma controlled on Global Initiative for Asthma (GINA) step 2 medication (ie, low dose inhaled corticosteroid [ICS] or leukotriene receptor antagonist [LTRA]), as evidenced by an asthma control questionnaire (ACQ-5) score ≤1.5, will be asked to stop their ongoing asthma maintenance treatment. After a washout period (14 to 21 days), all patients with confirmed reversibility will start study treatment, consisting of inhalations of AZD7594 (360 µg, delivered dose, via dry powder inhaler [DPI]) once daily for 15 to 16 days.

The study intends to include 24 patients in order to have 18 evaluable patients, enrolled in equal proportion in the age group of 12 to 14 years (inclusive), and the age group of 15 to 17 years (inclusive), with at least 7 patients in each subgroup.

For each patient, the duration of participation in the study will be approximately 5 to 7 weeks (37 to 52 days)

Studietype

Intervensjonell

Registrering (Faktiske)

36

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • California
      • Rolling Hills Estates, California, Forente stater, 90274
        • Research Site
    • Florida
      • Miami, Florida, Forente stater, 33165
        • Research Site
      • Miami Lakes, Florida, Forente stater, 33015
        • Research Site
    • Maryland
      • Bethesda, Maryland, Forente stater, 20814
        • Research Site
    • Missouri
      • Kansas City, Missouri, Forente stater, 64114
        • Research Site
    • Ohio
      • Columbus, Ohio, Forente stater, 43207
        • Research Site
    • Oklahoma
      • Oklahoma City, Oklahoma, Forente stater, 73106
        • Research Site
    • Texas
      • Boerne, Texas, Forente stater, 78006
        • Research Site
      • Dallas, Texas, Forente stater, 75225
        • Research Site
    • Utah
      • Murray, Utah, Forente stater, 84107
        • Research Site

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

12 år til 17 år (Barn)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  1. Provision of signed and dated informed consent form (ICF) prior to any study-specific procedures from patient's parents/legal guardians is required and signed and dated informed assent from the patient.
  2. Patient must be 12 to 17 years of age inclusive, at the time of signing the ICF/assent.
  3. A minimum of 6-month documented history of asthma treated (daily or intermittently) for at least 3 months before screening (Visit 1) with either low dose inhaled corticosteroid (ICS) monotherapy or leukotriene receptor antagonist (LTRA) monotherapy.
  4. Pre-bronchodilator FEV1 ≥70% of the predicted normal value at screening (Visit 1).
  5. An ACQ-5 score <1.5 at screening (Visit 1).
  6. Be non-smoker or ex-smoker who has stopped smoking (or using other nicotine products) for >6 months prior to screening (Visit 1).
  7. Body mass index (BMI) above the 5th percentile for the patient's age and gender and a minimum weight of 30 kg at screening (Visit 1).
  8. Male or female
  9. Negative pregnancy test (urine or serum) for post-menarcheal female patients at screening (Visit 1).
  10. Post-menarcheal female patients must be willing to use a highly effective method of contraception which results in a low failure rate (ie, less than 1% per year). Sexual abstinence will be accepted as an effective method of contraception, provided a discussion occurred between the subject and investigator to confirm this lifestyle.

    After the washout period, patients are eligible to enter the treatment period only if all of the following inclusion criteria apply:

  11. Negative pregnancy test (urine or serum) for post-menarcheal female patients at baseline (Visit 4).
  12. FEV1 increase of at least 12% and 200 mL from baseline 15 to 30 minutes after 400 μg salbutamol (or albuterol equivalent of 360 µg) documented in the patient's medical history within 6 months of Visit 1, or confirmed at Visit 1 or Visit 2. In 12 to 14-year-old patients (who are likely to have a smaller forced vital capacity), positive reversibility testing could be based solely on the relative post bronchodilator response (at least 12%).

Exclusion Criteria:

Patients are eligible to enter the washout period if none of the following exclusion criteria apply:

Medical conditions

  1. Any clinically significant disease or disorder (eg, cardiovascular, pulmonary other than asthma, gastrointestinal, liver, renal, neurological, musculoskeletal including bone fractures, endocrine including adrenal insufficiency, metabolic, malignant, psychiatric, major physical impairment, severe obesity including weight-related health problems) which, in the opinion of the Investigator, may either put the patient at risk because of participation in the study, or influence the result of the study, or the patient's ability to participate in the study.
  2. Any clinically relevant abnormal findings in physical examination, clinical chemistry, haematology, urinalysis, vital signs, at screening (Visit 1), which, in the opinion of the Investigator, may put the patient at risk because of his/her participation in the study.
  3. Prolonged QT interval corrected using Fridericia's formula (QTcF) ≥440 msec based on ECG at screening (Visit 1) or pre-dose at Visit 4, or family history of long QT syndrome.
  4. Prolonged PR interval (>180 msec for ≤16-year-old patients and >200 msec for >16 year old patients) at screening (Visit 1) or pre-dose at Visit 4.
  5. Heart rate <50 beats per minute (bpm) or >110 bpm.
  6. History of or current alcohol or drug abuse (including marijuana), as judged by the Investigator.
  7. Patients who are positive for hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibody or human immunodeficiency virus (HIV) at screening (Visit 1).
  8. Hospitalisation due to asthma exacerbation or asthma exacerbation within 1 month prior to screening (Visit 1).
  9. Lower respiratory tract infection within 1 month prior to screening (Visit 1).

    Prior/concomitant therapy

  10. Patient who, in the opinion of the Investigator, is unable to abstain from protocol-defined prohibited medications during the study.

    Prior/concurrent clinical study experience

  11. Participation in another clinical study with an investigational drug administered in the last 3 months before Visit 1, or participation in a method development study (no drug) 1 month prior to Visit 1.

    Note: Participation is identified as the completion of a treatment related visit.

  12. A definite or suspected personal history of intolerance or hypersensitivity to drugs and/or their excipients, judged to be clinically relevant by the Investigator.

    Other exclusions

  13. Inability to perform the required spirometry assessments, to use the AZD7594 inhaler or the short-acting beta agonist (SABA) inhaler, or to undergo blood sampling.
  14. Parent/legal guardian involvement in the planning and/or conduct of the study (applies to both AstraZeneca staff and/or staff at the study site).
  15. Judgement by the Investigator that the patient should not participate in the study if the patient is unlikely to comply with study procedures, restrictions and requirements.
  16. Previous enrolment in the present study.
  17. For post-menarcheal female patients only - currently pregnant, breastfeeding, or planning to become pregnant during the study.

After the washout period, patients are eligible to enter the treatment period if none of the following exclusion criteria apply:

  1. An ACQ-5 score ≥3 at Visit 4.
  2. SABA use of ≥12 puffs/day for ≥3 consecutive days during the washout period.
  3. An asthma exacerbation that required treatment with ICSs or systemic steroids during the washout period.
  4. A <70% compliance in completing asthma symptom score during the last 7 days of the washout period (ie, <5 out of 7 days with both morning and evening assessments completed).

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Cohort 1
The study will include adolescent patients of 12 to 17 years of age, with subgroups of 12-14 years age and 15-17 years age.
During treatment period, AZD7594 (360 µg per day) will be administered as oral inhalation via dry powder inhaler or DPI (SD3FL inhaler).

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Maximum observed plasma concentration at steady state (Cmax,ss) at Day 15 as part of PK evaluation
Tidsramme: Pre-dose and 15, 30 minutes, 2, 4, 6, 8, 12 hours post-dose at Day 15
To assess the PK profile of AZD7594 at steady state following daily inhalations for 2 weeks in adolescent patients with asthma
Pre-dose and 15, 30 minutes, 2, 4, 6, 8, 12 hours post-dose at Day 15
Minimum observed plasma concentration at steady state (Cmin,ss) at Day 15 as part of PK evaluation
Tidsramme: Pre-dose and 15, 30 minutes, 2, 4, 6, 8, 12 hours post-dose at Day 15
To assess the PK profile of AZD7594 at steady state following daily inhalations for 2 weeks in adolescent patients with asthma.
Pre-dose and 15, 30 minutes, 2, 4, 6, 8, 12 hours post-dose at Day 15
Observed trough plasma concentration at end of dosing interval (τ) (Ctrough) at Day 15 as part of PK evaluation
Tidsramme: Pre-dose and 15, 30 minutes, 2, 4, 6, 8, 12 hours post-dose at Day 15
To assess the PK profile of AZD7594 at steady state following daily inhalations for 2 weeks in adolescent patients with asthma
Pre-dose and 15, 30 minutes, 2, 4, 6, 8, 12 hours post-dose at Day 15
Time of maximum observed plasma concentration at steady state (tmax,ss) at Day 15 as part of PK evaluation
Tidsramme: Pre-dose and 15, 30 minutes, 2, 4, 6, 8, 12 hours post-dose at Day 15
To assess the PK profile of AZD7594 at steady state following daily inhalations for 2 weeks in adolescent patients with asthma.
Pre-dose and 15, 30 minutes, 2, 4, 6, 8, 12 hours post-dose at Day 15
Area under the plasma concentration-time curve over a dosing interval (τ) at steady state (AUCτ) at Day 15 as part of PK evaluation
Tidsramme: Pre-dose and 15, 30 minutes, 2, 4, 6, 8, 12 hours post-dose at Day 15
To assess the PK profile of AZD7594 at steady state following daily inhalations for 2 weeks in adolescent patients with asthma.
Pre-dose and 15, 30 minutes, 2, 4, 6, 8, 12 hours post-dose at Day 15
Area under the plasma concentration curve from time zero to 12 hours post-dose (AUC0-12) under plasma concentration at Day 15 as part of PK evaluation
Tidsramme: Pre-dose and 15, 30 minutes, 2, 4, 6, 8, 12 hours post-dose at Day 15
To assess the PK profile of AZD7594 at steady state following daily inhalations for 2 weeks in adolescent patients with asthma.
Pre-dose and 15, 30 minutes, 2, 4, 6, 8, 12 hours post-dose at Day 15
Apparent total body clearance after extravascular administration at steady state (CLss/F) at Day 15 as part of PK evaluation
Tidsramme: Pre-dose and 15, 30 minutes, 2, 4, 6, 8, 12 hours post-dose at Day 15
To assess the PK profile of AZD7594 at steady state following daily inhalations for 2 weeks in adolescent patients with asthma.
Pre-dose and 15, 30 minutes, 2, 4, 6, 8, 12 hours post-dose at Day 15

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Relative change from baseline in plasma cortisol area under the effect curve from time zero to 12 hours post-dose (AUEC0-12) on Day 15 as part of PD evaluation
Tidsramme: Pre-dose and 2, 4, 6, 8, 12 hours post-dose at Day 15
To evaluate the PD of AZD7594 following daily inhalations for 2 weeks in adolescent patients with asthma.
Pre-dose and 2, 4, 6, 8, 12 hours post-dose at Day 15
Change from baseline in morning trough forced expiratory volume in 1 second (FEV1) on Day 15 as part of PD evaluation
Tidsramme: At screening, Day 1 (pre-dose and 5, 15, 60 minutes post dose), Day 15 (pre-dose) and at end of study
To evaluate the PD of AZD7594 following daily inhalations for 2 weeks in adolescent patients with asthma.
At screening, Day 1 (pre-dose and 5, 15, 60 minutes post dose), Day 15 (pre-dose) and at end of study
Change from baseline in asthma control questionnaire (ACQ-5) on Day 15 as part of PD evaluation
Tidsramme: At screening, Day 1 (pre-dose) and Day 15 (pre-dose)
To evaluate the PD of AZD7594 following daily inhalations for 2 weeks in adolescent patients with asthma. ACQ-5 is a 5 item questionnaire that scores symptoms on a 0-6 scale (where 0=none/no symptoms and 6=worst symptoms) . The form is completed by the patient during visits.
At screening, Day 1 (pre-dose) and Day 15 (pre-dose)

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Number of patients with adverse events and abnormal findings in vital signs, clinical laboratory parameters, physical examination, and electrocardigram (ECG)
Tidsramme: From screening to follow-up (7-14 days)
To evaluate the tolerability and safety of inhaled AZD7594
From screening to follow-up (7-14 days)

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Samarbeidspartnere

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

24. juli 2019

Primær fullføring (Faktiske)

9. juli 2020

Studiet fullført (Faktiske)

9. juli 2020

Datoer for studieregistrering

Først innsendt

5. juni 2019

Først innsendt som oppfylte QC-kriteriene

5. juni 2019

Først lagt ut (Faktiske)

6. juni 2019

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

29. januar 2021

Siste oppdatering sendt inn som oppfylte QC-kriteriene

27. januar 2021

Sist bekreftet

1. januar 2021

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

JA

IPD-planbeskrivelse

Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca group of companies sponsored clinical trials via the request portal. All request will be evaluated as per the AZ disclosure commitment: https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.

Yes, indicates that AZ are accepting requests for IPD, but this does not mean all requests will be shared.

IPD-delingstidsramme

AstraZeneca will meet or exceed data availability as per the commitments made to the EFPIA Pharma Data Sharing Principles. For details of our timelines, please rerefer to our disclosure commitment at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.

Tilgangskriterier for IPD-deling

When a request has been approved AstraZeneca will provide access to the de-identified individual patient-level data in an approved sponsored tool . Signed Data Sharing Agreement (non-negotiable contract for data accessors) must be in place before accessing requested information. Additionally, all users will need to accept the terms and conditions of the SAS MSE to gain access. For additional details, please review the Disclosure Statements at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Ja

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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