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Completed

NCT Number: NCT02787967

Clinical Pharmacology of 35/4 NEXThaler® in Children 5-11 Years Old

The study will be conducted in asthmatic children aged 5 to 11 years and is based on a single-dose, open-label, randomized, 2-way cross-over design where a Dry Powder Inhaler (DPI) fixed combination of beclometasone dipropionate (BDP) 35 μg plus formoterol fumarate (FF) 4 μg is compared with the free combination of licensed BDP DPI and FF DPI

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Key information

Age range

5 year–11 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

BørneAstmaKlinikken, Hans Knudsens Plads 1A,

Copenhagen, Denmark

About this study

This is a pharmacokinetic comparison of NEXThaler 35/4 μg versus the free combination of Beclomethasone DPI and Formoterol DPI in children (5 to 11 years old) of a formulation already approved in adults.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male/female children with asthma stable enough, according to paediatrician opinion, to allow a wash out period from steroids of 3 days before study treatments.
  • Male/female children with asthma on regular treatment with ICS or using short-acting inhaled 2-agonist as reliever to control asthma symptoms.
  • Age ≥ 5 < 12 years (8 to 10 children in the age range 5-8 years old).
  • Children with a forced expiratory volume in one second (FEV1)>70% of predicted values (% pred) after withholding 2-agonists treatment for a minimum of 4 h prior to screening and to each study treatment.
  • A cooperative attitude and ability to be trained about the proper use of DPI, ability to use correctly the medical devices and compliant to study procedures

Exclusion criteria

  • Past or present diagnosis of cardiovascular, renal or liver disease.
  • Known hypersensitivity to the active treatmen
  • Exacerbation of asthma symptoms within 4 weeks prior to screening.
  • Inability to perform the required breathing technique and blood sampling.
  • Hospitalization due to exacerbation of asthma within 1 month prior to screening (Visit 1).
  • Lower respiratory tract infection within 1 month prior to screening (Visit 1).
  • Disease (other than asthma) which might influence the outcome of the study.
  • Obesity, i.e. > 97% weight percentile by local standards

Treatment and study plan

CHF 1535 35/4µg NEXThaler®

Drug

4 (four) inhalations (total dose: BDP/FF 140/16 µg)

free comb. beclomethasone DPI and formoterol DPI

Drug

2 (two) inhalations BDP 100 µg DPI + 4 (four) inhalations FF 6 µg DPI (total dose: BDP 200 µg + FF 24 µg

Primary outcomes

  1. Plasma Area Under Curve (AUC0-t) for B17MP, active metabolite of BDP

    Time frame: predose, 15,30min, 1,2,4,6,8 hours post dose

    B17MP: Profile of Pharmacokinetics

Secondary outcomes

  1. B17MP Cmax

    Time frame: predose, 15min,30min,1,2,4,6,8 hours post dose

    17MP: profile of pharmacokinetics

  2. BDP Area Under Curve (AUC)

    Time frame: predose, 15min,30min,1,2,4,6,8 hours post dose

    BDP: profile of Pharmacokinetics

  3. Formoterol Area Under Curve (AUC), Cmax, Tmax, T1/2 [

    Time frame: predose, 15min, 30 min, 1,2,4,6,8 hours postdose

    Formoterol: profile of pharmacokinetics

  4. Formoterol Cmax

    Time frame: predose, 15min, 30 min, 1,2,4,6,8 hours postdose

    Formoterol: profile of pharmacokinetics

  5. Formoterol Tmax

    Time frame: predose, 15min, 30 min, 1,2,4,6,8 hours postdose

    Formoterol: profile of pharmacokinetics

  6. Formoterol T1/2

    Time frame: predose, 15min, 30 min, 1,2,4,6,8 hours postdose

    Formoterol: profile of pharmacokinetics

  7. plasma potassium Area Under Curve (AUC)

    Time frame: predose, 15min, 30min, 1, 2, 4, 6, 8 hours postdose

    plasma potassium to evaluate drug systemic effect

  8. plasma potassium Cmin

    Time frame: predose, 15min, 30min, 1, 2, 4, 6, 8 hours postdose

    plasma potassium to evaluate drug systemic effect

  9. plasma potassium Tmin

    Time frame: predose, 15min, 30min, 1, 2, 4, 6, 8 hours postdose

    plasma potassium to evaluate drug systemic effect

  10. Urinary Cortisol: Amount excreted in 0-8hours (Ae),8h cortisol urinary excretion normalized for 8h creatinine excretion (Ae/Aecreat).

    Time frame: from predose up to 8 hours postdose

    Urinary cortisol to evaluate drug systemic effect

  11. B17MP Tmax

    Time frame: predose, 15min,30min,1,2,4,6,8 hours post dose

    BDP: profile of pharmacokinetics

  12. B17MP T1/2

    Time frame: predose, 15min,30min,1,2,4,6,8 hours post dose

    BDP: profile of pharmacokinetics

  13. BDP Cmax

    Time frame: predose, 15min,30min,1,2,4,6,8 hours post dose

    BDP: profile of pharmacokinetics

  14. BDP Tmax

    Time frame: predose, 15min,30min,1,2,4,6,8 hours post dose

    BDP: profile of pharmacokinetics

  15. BDP T1/2

    Time frame: predose, 15min,30min,1,2,4,6,8 hours post dose

    BDP: profile of pharmacokinetics

Sponsors and collaborators

Lead sponsor

Chiesi Farmaceutici S.p.A.

Industry

Registry information

Official study title

A Single-dose, Open-label, Randomized, 2-way Cross-over Study of CHF 1535 35/4 NEXThaler® (Fixed Combination of Beclometasone Dipropionate (BDP) 35 μg Plus Formoterol Fumarate (FF) 4 μg Versus the Free Combination of Licensed BDP DPI (Dry Powder Inhaler) and FF DPI in Asthmatic Children

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Jun 2, 2016
Registry last updated
Feb 5, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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