Pharmacokinetics and pharmacodynamics of an extrafine fixed pMDI combination of beclometasone dipropionate/formoterol fumarate in adolescent asthma. (1st June 2015)
- Record Type:
- Journal Article
- Title:
- Pharmacokinetics and pharmacodynamics of an extrafine fixed pMDI combination of beclometasone dipropionate/formoterol fumarate in adolescent asthma. (1st June 2015)
- Main Title:
- Pharmacokinetics and pharmacodynamics of an extrafine fixed pMDI combination of beclometasone dipropionate/formoterol fumarate in adolescent asthma
- Authors:
- Kuna, Piotr
Govoni, Mirco
Lucci, Germano
Scuri, Mario
Acerbi, Daniela
Stelmach, Iwona - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="bcp12640-sec-0001" sec-type="section"> <title>Aim</title> <p>The aim was to investigate the pharmacokinetics and pharmacodynamics of an extrafine pressurized metered‐dose inhaler (pMDI) fixed combination of beclometasone dipropionate (BDP)/formoterol fumarate (FF) in adolescent and adult asthma.</p> </sec> <sec id="bcp12640-sec-0002" sec-type="section"> <title>Methods</title> <p>This was a three‐way crossover study, on 30 asthmatic adolescents receiving BDP/FF pMDI with or without a valved holding chamber (VHC) or a free licenced combination of BDP pMDI and FF pMDI plus a parallel arm of 30 asthmatic adults receiving BDP/FF pMDI. All patients received a single dose of BDP and FF of 400 µg and 24 µg, for each treatment, respectively. Assessments were performed over 8 hours.</p> </sec> <sec id="bcp12640-sec-0003" sec-type="section"> <title>Results</title> <p>In adolescents, the 90% confidence intervals (CIs) for the systemic exposure (AUC(0, <italic>t</italic>)) geometric mean ratio of the fixed combination with or without VHC <italic>vs</italic>. the free combination were within the bioequivalence range 0.80–1.25, both for beclometasone‐17‐monopropionate (B17MP, the active metabolite of BDP) and formoterol. Pharmacodynamic variables for plasma potassium and glucose, pulse rate and pulmonary function in adolescents were equivalent between treatments, 95% CI within 0.9, 1.09. The<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="bcp12640-sec-0001" sec-type="section"> <title>Aim</title> <p>The aim was to investigate the pharmacokinetics and pharmacodynamics of an extrafine pressurized metered‐dose inhaler (pMDI) fixed combination of beclometasone dipropionate (BDP)/formoterol fumarate (FF) in adolescent and adult asthma.</p> </sec> <sec id="bcp12640-sec-0002" sec-type="section"> <title>Methods</title> <p>This was a three‐way crossover study, on 30 asthmatic adolescents receiving BDP/FF pMDI with or without a valved holding chamber (VHC) or a free licenced combination of BDP pMDI and FF pMDI plus a parallel arm of 30 asthmatic adults receiving BDP/FF pMDI. All patients received a single dose of BDP and FF of 400 µg and 24 µg, for each treatment, respectively. Assessments were performed over 8 hours.</p> </sec> <sec id="bcp12640-sec-0003" sec-type="section"> <title>Results</title> <p>In adolescents, the 90% confidence intervals (CIs) for the systemic exposure (AUC(0, <italic>t</italic>)) geometric mean ratio of the fixed combination with or without VHC <italic>vs</italic>. the free combination were within the bioequivalence range 0.80–1.25, both for beclometasone‐17‐monopropionate (B17MP, the active metabolite of BDP) and formoterol. Pharmacodynamic variables for plasma potassium and glucose, pulse rate and pulmonary function in adolescents were equivalent between treatments, 95% CI within 0.9, 1.09. The upper level of 90% CIs for AUC(0, <italic>t</italic>) geometric mean ratio adolescents : adults of B17MP and formoterol after treatment with BDP/FF pMDI was lower than 1.25, 90% CI 0.78, 1.04 and 0.86, 1.17, respectively.</p> </sec> <sec id="bcp12640-sec-0004" sec-type="section"> <title>Conclusions</title> <p>In adolescents the pharmacodynamics and the overall systemic exposure to the active ingredients of an extrafine fixed combination of BDP/FF pMDI with or without a VHC was equivalent to that of a free licenced combination of pMDIs of established safety and efficacy profiles. The systemic exposure in adolescents was not higher than in adults. These results support the indication for use of inhaled corticosteroid/long acting β<sub>2</sub>‐adrenoceptor agonist pMDIs in adolescents at the same dosage as in adults.</p> </sec> </abstract> … (more)
- Is Part Of:
- British journal of clinical pharmacology. Volume 80:Number 3(2015:Sep.)
- Journal:
- British journal of clinical pharmacology
- Issue:
- Volume 80:Number 3(2015:Sep.)
- Issue Display:
- Volume 80, Issue 3 (2015)
- Year:
- 2015
- Volume:
- 80
- Issue:
- 3
- Issue Sort Value:
- 2015-0080-0003-0000
- Page Start:
- 569
- Page End:
- 580
- Publication Date:
- 2015-06-01
- Subjects:
- Pharmacology -- Periodicals
Drugs -- Periodicals
615.1 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2125 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/bcp.12640 ↗
- Languages:
- English
- ISSNs:
- 0306-5251
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2307.180000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3476.xml