An Efficacy and Safety Study to Assess an Inhaled, Fixed-dose, Budesonide/Formoterol Fumarate in Participants Aged 4 to Less Than 12 Years of Age With Moderate Persistent Asthma (SOLAIR)
A 6-week, Double-blind, Randomized, Parallel-group, Multicenter Study to Evaluate the Efficacy and Safety of Symbicort Aerosphere (BFF) 80/4.8 μg 2 Actuations BID Relative to Budesonide (BD) 80 μg 2 Actuations BID, in Participants Aged 4 to < 12 Years With Moderate Persistent Asthma
The purpose of this study is to evaluate whether budesonide and formoterol fumarate (BFF) metered-dose inhaler (MDI) is superior to BD MDI in improving lung function 1 hour post dose at Week 6 in children aged 4 to less than 12 years with moderate persistent asthma. The study will also assess safety of BFF MDI over a 6-week treatment period.
Visão geral do estudo
Status
Status
Condições
Condições
Intervenção / Tratamento
Intervenção / Tratamento
Descrição detalhada
This is a 6-week, parallel-group, active-controlled, multicenter, study comparing BFF MDI 80/4.8 μg, 2 actuations twice daily (BID), to BD MDI 80 μg, 2 actuations BID.
The study will consist of:
- An enrollment visit (Visit 1a)
- A run-in period (beginning at Visit 1b): During the run-in period (2 weeks) participants will receive BD MDI BID as asthma maintenance therapy plus as needed short-acting β2-agonist (SABA) only.
- A randomization visit (Visit 2): At this visit, participants will be randomized in a 1:1 scheme to one of two treatment arms: (i) BFF 80/4.8 μg 2 actuations BID plus as needed SABA (ii) BD 80 μg 2 actuations BID plus as needed SABA.
- Visit 3 (2 weeks post randomization): A telephone call or tele-visit depending on participant convenience and preference to assess asthma status and adherence to study intervention.
- Visit 4 (6 weeks post randomization): At this visit, participants will receive their final dose of study intervention and lung function will be assessed. Following this visit, participants will switch back to their pre-study asthma maintenance therapy.
- Visit 5 (approximately 2 weeks post study completion) is a telephone call or tele-visit to record/follow-up any adverse events (AEs) experienced by the participant and to record any concomitant medications following Visit 5.
Tipo de estudo
Tipo de estudo
Inscrição (Estimado)
Inscrição
Estágio
Estágio
- Fase 3
Contactos e Locais
Contato de estudo
Contato de estudo
- Nome: AstraZeneca Clinical Study Information Center
- Número de telefone: 1-877-240-9479
- E-mail: information.center@astrazeneca.com
Critérios de participação
Critérios de elegibilidade
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
Inclusion Criteria:
- Have a documented clinical diagnosis of asthma as defined by the American Thoracic Society (ATS) for at least 6 months prior to Visit 1a.
- Had no asthma exacerbations requiring an escalation of inhaled medication regimen, systemic corticosteroids or hospitalization in the 6 months prior to Visit 1a.
- Body mass index (BMI) ≤95 percentile for age and sex.
- Female participants who have reached menarche must have a negative urine pregnancy test at all study site visits.
- If receiving immunotherapy per injection or sublingual, a participant must have been on a stable maintenance regimen for at least 6 weeks and be expected to remain on immunotherapy throughout the study.
- Require and are prescribed treatment with a consistent daily dose of inhaled ICS with or without LABA for at least 4 weeks prior to Visit 1a with doses including: Beclometasone dipropionate >200-400 μg/day (standard particle) or >100-200 μg/day (extra fine), BD dipronponate [dry-powder inhaler (DPI), or pressurized metered dose inhaler (pMDI), standard particle, hydrofluoroalkane (HFA)] >200 to 400 μg/day or BD (nebules) >500 to 1000 μg/day, Ciclesonide >80-160 μg/day, Fluticasone furoate 50 μg/day, Fluticasone propionate >100-200 μg/day, or Mometasone furoate 100 μg/day.
- Site-measured FEV1 at morning pre-bronchodilator visit must be ≥60% of the predicted normal, taken at least 6 hours after the last inhaled SABA, and at least 48 hours after the last inhaled LABA prior to Visit 1b. At Visit 2, pre-dose morning FEV1 should be ≥60% predicted normal value. Additionally, the FEV1 should not decrease by more than 10% in absolute value [liter [L]) from measurement at Visit 1b.
- Participants must demonstrate bronchodilator reversibility of ≥10% increase in FEV1 within 15-30 minutes after albuterol/salbutamol administration (90/100 μg per inhalation, 4 actuations with spacer) at the study site (repeatable once if initially failed), OR have historical reversibility of ≥10% within 1 year, OR show 10% FEV1 variability between site visits within 12 months with morning pre-bronchodilator FEV1 ≤95% predicted, OR if bronchodilator response is 7-<10% with post-bronchodilator FEV1 <95% predicted, meet at least one of: positive Methacholine Challenge Test (PC20 ≤16 mg/mL), peak expiratory flow (PEF) daily diurnal variability >13% over 2 weeks, positive exercise challenge test (FEV1 decrease >12%), or fractional exhaled nitric oxide ≥20 ppb despite ICS maintenance.
- Demonstrated ability to use any study devices [MDI with or without spacer, peak expiratory flow meter (PEFM)]. Participants aged 4 to 6 years are mandated to use a spacer. Participants older than 6 years of age must demonstrate adequate MDI technique or use a spacer if failed to demonstrate adequate technique after an objective testing.
- Had discontinued use of all asthma medications, including all formulations of β2-agonists, and used only the run-in medication and rescue medication provided since Visit 1b.
Exclusion Criteria:
- Had been hospitalized at least once or required emergency treatment more than once for an asthma-related condition during the 6 months prior to Visit 1a.
- Had any significant disease or disorder (eg, cardiovascular, pulmonary [other than asthma], gastrointestinal, hepatic, renal, neurological, musculoskeletal, endocrine, metabolic, malignant, psychiatric, major physical impairment) or other disease or condition generally affecting lung function (eg, prematurity, congenital lung anomalies, tracheoesophageal fistula, bronchiectasis, chronic sinusitis).
- Had a known or suspected hypersensitivity to albuterol/salbutamol, or BD, or FF, and/or their excipients and/or have a severe hypersensitivity to milk proteins.
- Had any clinically relevant abnormal findings in physical examination, vital signs, abnormalities in electrocardiogram (ECG) or laboratory results at Visit 1a/Visit 1b.
- Had a respiratory infection or other viral/bacterial illness or were recovering from such an illness at the time of Visit 2.
- Loss of asthma stability between Visit 1 and Visit 2, characterized by ≥6 inhalations of SABA within any 24-hour period, ≥4 inhalations of SABA within any 4-hour period, night-time awakenings due to asthma on ≥2 nights per week, daytime symptoms on >2 days per week or limitation in normal activity on ≥2 days per week, ≥20% decrease in PEF from screening baseline, or any unscheduled physician, urgent care, or emergency department visit for asthma.
- Have a planned hospitalization at any time during the study.
- Receiving treatment with a β-blocker (including eye-drops).
- Had taken any other monoclonal or polyclonal antibody therapy, for any reason within the 6 months prior to Visit 1b.
- Had been treated with systemic corticosteroids (eg oral, parenteral, or rectal).
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Triplo
Número de braços
Armas e Intervenções
Grupo de Participantes / BraçoGrupo de Participantes / Braço |
Intervenção / TratamentoIntervenção / Tratamento |
|---|---|
|
Experimental: Budesonide and formoterol fumarate metered-dose inhaler (BFF MDI)
Participants will receive oral inhalations of BFF MDI 80/4.8 μg as 2 actuations BID. |
BFF pressurized inhalation suspension will be administered as 2 oral actuations.
Outros nomes:
|
|
Comparador Ativo: Budesonide metered-dose inhaler (BD MDI)
Participants will receive oral inhalations of BD MDI 80 μg as 2 actuations BID. |
BD pressurized inhalation suspension will be administered as 2 oral actuations. |
O que o estudo está medindo?
Medidas de resultados primários
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Change from baseline in 1 hour post dose forced expiratory volume in the first second (FEV1) at Week 6
Prazo: At Week 6
|
The effect of BFF MDI 80/4.8 μg 2 actuations BID relative to BD MDI 80 μg 2 actuations BID on post dose lung function at Week 6 in participants 4 to less than 12 years of age with moderate persistent asthma will be assessed. |
At Week 6
|
Medidas de resultados secundários
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Change from baseline in 1 hour post dose FEV1 at Day 1
Prazo: On Day 1
|
The effect of BFF MDI 80/4.8 μg 2 actuations BID relative to BD MDI 80 μg 2 actuations BID on post dose lung function at Day 1 in participants 4 to less than 12 years of age with moderate persistent asthma will be assessed. |
On Day 1
|
|
Change from baseline in 15 minutes post dose FEV1 at Week 6
Prazo: At Week 6
|
The effect of BFF MDI 80/4.8 μg 2 actuations BID relative to BD MDI 80 μg 2 actuations BID on post dose lung function at Week 6 in participants 4 to less than 12 years of age with moderate persistent asthma will be assessed. |
At Week 6
|
|
Change from baseline in morning pre-dose FEV1 at Week 6
Prazo: At Week 6
|
The effect of BFF MDI 80/4.8 μg 2 actuations BID relative to BD MDI 80 μg 2 actuations BID on pre-dose lung function at Week 6 in participants 4 to less than 12 years of age with moderate persistent asthma will be assessed. |
At Week 6
|
Outras medidas de resultado
Outras medidas de resultado
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Number and percentage of participants with adverse events (AEs), serious adverse events (SAEs) and AEs leading to discontinuation (DAEs)
Prazo: From run-in period (Visit 1b) and up to the follow-up telephone call [2 weeks (± 5 days) after last dose of study intervention] (up to 10 weeks after the start of run-in)
|
Safety and tolerability of BFF MDI 80/4.8 μg 2 actuations BID versus BD MDI 80 μg 2 actuations BID in participants 4 to less than 12 years of age with moderate persistent asthma will be compared. |
From run-in period (Visit 1b) and up to the follow-up telephone call [2 weeks (± 5 days) after last dose of study intervention] (up to 10 weeks after the start of run-in)
|
Colaboradores e Investigadores
Patrocinador
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Início do estudo
Conclusão Primária (Estimado)
Conclusão Primária
Conclusão do estudo (Estimado)
Conclusão do estudo
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Primeira postagem
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última Atualização Postada
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
Outros números de identificação do estudo
- D7820C00004
- 5570196 (Outro identificador: Pediatric Study Plan Number)
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Descrição do plano IPD
Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca group of companies sponsored clinical trials via the request portal Vivli.org. All requests 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.
Prazo de Compartilhamento de IPD
AstraZeneca will meet or exceed data availability as per the commitments made to the EFPIA PhRMA Data Sharing Principles. For details of our timelines, please rerefer to our disclosure commitment at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
Critérios de acesso de compartilhamento IPD
When a request has been approved AstraZeneca will provide access to the anonymized individual patient-level data via secure research environment Vivli.org. Signed Data Usage Agreement (non-negotiable contract for data accessors) must be in place before accessing requested information.
Tipo de informação de suporte de compartilhamento de IPD
- PROTOCOLO DE ESTUDO
- SEIVA
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