Knemometry Study to Compare the Systemic Safety of Flutiform pMDI, Fluticasone pMDI and Beclometasone Autohaler in Paediatric Subjects Aged 5 to Less Than 12 Years.

NCT02063139 | Completed Phase 2

• 2 other identifiers: FLT25042013-004719-32
• Study Type: interventional
• Target: 48
• Locations: 1 country
• Sites: 1

Brief Summary

Aim of the study is to investigate the short-term growth in children with asthma aged 5-11 years in treatment with fluticasone propionate / formoterol spray (flutiform®) 200/20 micrograms per day

Conditions

Mild Persistent Asthma

Keywords

Knemometry

Outcome Measures

Primary Outcomes (1)

• To show non-inferiority of flutiform pMDI 50/5 µg (2 puffs bid) versus fluticasone pMDI 50 µg (2 puffs bid) based on the mean lower leg growth rates.

  Lower leg length will be measured in the afternoon, between 13:00 and 19:00h. Each individual subject will have their knemometry measurements performed at the same time of day (+/- 1 hour).

  Change from baseline in growth rate during the each treatment and washout period which is 2 weeks

Secondary Outcomes (1)

• To compare the safety of flutiform pMDI 50/5 µg (2 puffs bid) versus fluticasone pMDI 50 µg based on overnight urinary free cortisol (corrected for creatinine).

  every two weeks for duration of study which is two months.

Study Arms (3)

Flutiform 50/5 ug (2 puffs bid) pMDI

EXPERIMENTAL

Flutiform 50/5 ug (2 puffs bid) pMDI

Drug: Flutiform 50/5 ug (2 puffs bid) pMDI

Fluticasone 50 ug (2puffs bid) pMDI

ACTIVE COMPARATOR

Fluticasone 50 ug (2puffs bid) pMDI

Drug: Fluticasone 50 ug (2puffs bid) pMDI

Beclometasone Autohaler 50 ug (2 puffs bid)

OTHER

Active control

Drug: Beclometasone Autohaler 50 ug (2 puffs bid)

Interventions

Flutiform 50/5 ug (2 puffs bid) pMDI DRUG

Flutiform 50/5 ug (2 puffs bid) pMDI

Fluticasone 50 ug (2puffs bid) pMDI DRUG

Fluticasone 50 ug (2puffs bid) pMDI

Beclometasone Autohaler 50 ug (2 puffs bid) DRUG

Beclometasone Autohaler 50 ug (2 puffs bid)

Eligibility Criteria

• Age: 5 Years - 12 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17)

You may qualify if:

• Subjects to be included in the study are those who meet all of the following criteria:
• Male and Female subjects 5 to \<12 years old. Female subjects must be pre-menarche to be eligible.
• Subjects must be pre-adolescent without any signs of puberty (acc. to Tanner scale).
• Subjects are in normal range for their age in height and weight. Weight and height measurements should fall within the percentile range 3-97-% of normal values for age according to Danish growth charts.
• Known history of mild intermittent or persistent reversible asthma for ≥ 3 months prior to the screening visit.
• Require:
• only inhaled SABA therapy (e.g. Bricanyl Turbuhaler) on an as required basis, and/or
• Regular non-ICS controller medications for asthma (e.g., cromones or leukotriene receptor antagonists) at a stable dose for ≥ 3 months prior to the screening visit.
• No ICS for \>2 weeks prior to the screening visit.
• Demonstrates adequate spirometry technique and able to use a home PEFR meter.
• Demonstrated FEV1 of ≥ 80% predicted value at visit 1following appropriate withholding of asthma medications (if applicable) (no SABA use within 6 hours of the PFT).
• Demonstrated satisfactory technique in the use of the pMDI plus spacer and Autohaler devices.
• Must be continent of urine and willing to perform (with parental/guardian help) overnight urine collections.
• Willing and able to complete morning and evening PEFR measures with the help of a parent or guardian, if necessary, and attend all study visits.
• Willing and able to substitute pre-study prescribed inhaled asthma medication for the entire duration of the study with study medication.

You may not qualify if:

• Subjects to be excluded from the study are those who meet any of the following criteria:
• Require medications other than inhaled SABAs and/or regular non-ICS controller medications (e.g., cromones or leukotriene receptor antagonists) to maintain asthma control.
• ICS use within ≤ 2 weeks prior to the screening visit.
• Any asthma exacerbation of any severity for at least 3 months prior to the screening visit.
• Any fracture in the leg to be measured by knemometry ≤6 months prior to the screening visit.
• Any metabolic disorders or other diseases that may impact on normal growth patterns.
• Near fatal or life-threatening asthma within the past year.
• Hospitalisation or an emergency visit for asthma within the past 6 months.
• History of oral or injectable corticosteroid medication ≤3 months prior to the screening visit.
• Evidence of a clinically unstable disease, as determined by medical history, clinical laboratory tests, and physical examination that, in the Investigator's opinion, preclude entry into the study. "Clinically significant" is defined as any disease that, in the opinion of the Investigator, would put the subject at risk through study participation, or which would affect the outcome of the study.
• No major surgery requiring general anesthesia for at least 3 months prior to the screening visit.
• No febrile illnesses with temperature \> 39°C within a week of the screening visit.
• In the Investigator's opinion a clinically significant upper or lower respiratory infection within 4 weeks prior to the screening visit.
• Significant, non-reversible active pulmonary disease (e.g. cystic fibrosis, bronchiectasis, tuberculosis).
• Subjects who have taken β- blocking agents, tricyclic antidepressants, monoamine oxidase inhibitors, astemizole (Hismanal), quinidine type antiarrythmics, or potent CYP 3A4 inhibitors such as ketoconazole within 1 week prior to the screening visit.

Sponsors & Collaborators

• Mundipharma Research Limited: lead

Study Sites (1)

Asthma and Allergy Children's Clinic

Randers, Denmark

Location

Related Publications (1)

• Wolthers OD, Mersmann S, Dissanayake S. A Pilot Study of the Normative Range of Overnight Urinary Free Cortisol Corrected for Creatinine in Children. Clin Drug Investig. 2018 Apr;38(4):313-318. doi: 10.1007/s40261-017-0609-x.

  PMID: 29256049 DERIVED

Related Links

• Results available on register

MeSH Terms

Interventions

fluticasone-formoterol; Fluticasone

Intervention Hierarchy (Ancestors)

Androstadienes; Androstenes; Androstanes; Steroids; Fused-Ring Compounds; Polycyclic Compounds

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: CROSSOVER
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: February 11, 2014
• First Posted: February 14, 2014
• Study Start: February 1, 2014
• Primary Completion: June 1, 2014
• Study Completion: January 1, 2015
• Last Updated: October 24, 2018

Record last verified: 2018-10

Locations

DK (1)