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Anakinra Rescue Treatment for Moderate Asthma Attacks (ARTMA) (ARTMA)

13 de julho de 2026 atualizado por: University of North Carolina, Chapel Hill

Anakinra Rescue Treatment for Moderate Asthma Attacks (ARTMA) Pilot Study

In this single center, interventional pilot study, 40 participants at high risk for future exacerbation will be randomized to anakinra (v. placebo control) treatment for home administration as part of an asthma action plan (AAP) and monitored through their first moderate asthma exacerbation, triggering treatment dosing over a 26 week period. Key feasibility questions will be assessed in this pilot study to inform trial design and sample size selection for a future multi-site phase II clinical trial testing anakinra as a rescue treatment for moderate asthma exacerbations.

Visão geral do estudo

Descrição detalhada

This pilot study will incorporate early intervention with the IL-1 receptor antagonist (IL-1RA), anakinra, as part of a home-based asthma action plan (AAP) at the start of a moderate exacerbation with the goal of preventing severe exacerbations requiring systemic steroids. The investigators will determine the feasibility of recruitment, enrollment, and retention for a trial that requires self administered injections; adherence to critical protocol operational tasks and rates of moderate exacerbations; and preliminary safety and efficacy of anakinra treatment during a moderate asthma exacerbation, with the goal of these findings supporting the development a hybrid decentralized phase II trial.

40 adults (≥18 years and < 65 years) with persistent asthma that experienced an exacerbation within the prior 12 months requiring systemic steroid treatment will be enrolled, with the aim to randomize 20 women and 20 men. Up to 100 subjects will be screened to randomize 40 subjects.

Patients are to receive anakinra or placebo during a moderate asthma exacerbation (defined by pre-specified criteria). Investigators will monitor symptom scores, lung function measurements, rescue medication use, systemic corticosteroid use, and healthcare utilization during exacerbations. Device training, blood collection, and nasal sample collection will also occur.

Tipo de estudo

Intervencional

Inscrição (Estimado)

60

Estágio

  • Fase 1

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Estude backup de contato

Locais de estudo

    • North Carolina
      • Chapel Hill, North Carolina, Estados Unidos, 27599
        • University of North Carolina Chapel Hill
        • Investigador principal:
          • Michelle Hernandez, MD
        • Contato:
        • Contato:

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  • Provision of signed and dated informed consent form
  • Age ≥18 years
  • A history of physician-diagnosed persistent asthma or symptoms consistent with persistent asthma based on national or international guidelines for diagnosis and management of asthma.
  • Current use of controller therapy such as inhaled corticosteroid (ICS) or ICS in combination with long-acting beta agonist (LABA)
  • Asthma exacerbation requiring systemic corticosteroid therapy in the past 12 months
  • Negative pregnancy test for females who are not s/p hysterectomy with oophorectomy or who have been amenorrheic for 12 months or more.
  • Asthma Impairment and Risk Questionnaire (AIRQ) Score >2

Exclusion Criteria:

  • Clinical contraindications:

    1. Physician diagnosis of other chronic pulmonary disease including cystic fibrosis (CF), chronic obstructive pulmonary disease (COPD), chronic bronchitis, emphysema or congenital disorders of the lungs or airways.
    2. History of undergoing bronchial thermoplasty.
    3. Intubation for asthma in the last 12 months
    4. History of malignancy except non-melanoma skin cancer within the last five years.
    5. Any chronic medical condition considered by the PI as a contraindication to inclusion in the study including significant cardiovascular disease, diabetes, chronic renal disease, chronic thyroid disease, history of chronic or recurrent infections or immunodeficiency.
    6. Mental illness or history of substance abuse that, in the opinion of the investigator, would interfere with the participant's ability to comply with study requirements.
    7. History of smoking: i. Smoking >1 time per week in the past year; ii. If ≥40 years old: Smoked ≥15 pack years; iii. If <40 years old: Smoked ≥10 pack years; iv. Smoking equivalents of 1 pack cigarettes a day for 1 year: 1 cigar or pipe daily for 1 year; Hookah - 1 session per day for 1 year; E-cigarettes or vapes - 1 cartridge/tank/pod per day for 1 year; and active use of smoking/vaping marijuana, specified as once per week in the last year.
    8. Allergy/sensitivity to study drugs or their formulations, including latex
    9. Unwillingness to use reliable contraception if sexually active (IUD, birth control pills/patch, condoms).
    10. Current participation in an interventional trial in which study administration was administered within the past 60 days or within 5 half-lives of the drug (whichever is greater)
  • Pregnancy, plans to get pregnant or nursing a baby. Female volunteers will be asked to use effective birth control (stable regimen of hormonal contraceptive use for at least 6 months, intrauterine device placement, or tubal ligation for at least 6 months through at least one week after study completion) and will provide a urine sample to test for pregnancy on study days. If the test is positive or the participant has reason to believe she may be pregnant, she will be dismissed from the study. Women who have been amenorrheic for 12 months may participate. Male volunteers will be asked to use condoms for the duration of the study through at least one week after study completion.
  • Usage of the following medications:

    1. Use of daily systemic corticosteroid therapy for asthma control
    2. Use of any immunomodulatory therapy within the preceding 12 months, including biologics that are approved for asthma.
    3. Currently receiving allergen immunotherapy
    4. Use of any immunosuppressant therapy within the preceding 12 months will be reviewed by the study physician.
  • Laboratory: Participants who meet the following criteria will be excluded from study:

    1. Positive QuantiFERON-tuberculosis (TB) gold assay. Cases of indeterminate QuantiFERON-TB test results will require a second specimen to be drawn.
    2. Baseline absolute neutrophil count (ANC) <1.0 x 109/L for participants of African descent, <1.5 x 109/L for other participants
  • Allergy/sensitivity to study drugs or their formulations, including latex.
  • History of anaphylaxis requiring epinephrine treatment
  • Inability or unwillingness of a participant to give written informed consent.
  • Inability or unwillingness to self-administer injectable medication (anakinra or placebo).

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Quadruplicar

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador Ativo: Active Treatment
Subjects will be randomized to receive two doses of active study treatment (anakinra) upon meeting orange zone exacerbation criteria.
Active study treatment
Comparador de Placebo: Placebo
Subjects will be randomized to receive two doses of placebo upon meeting orange zone exacerbation criteria.
Placebo

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Study Design Feasibility - Percentage of participants who experience one moderate asthma exacerbation
Prazo: The 6-month period from randomization to the end of study visit
Percent of randomized participants who experience one moderate asthma exacerbation (as defined by the participant's asthma action plan) during the 6-month study period.
The 6-month period from randomization to the end of study visit
Effect of Anakinra on absolute change in morning PEF from baseline during moderate asthma exacerbation
Prazo: Day 1 of treatment through day 10 after treatment
Area under the curve (AUC) of the absolute change from baseline, over the period of treatment day 1 through 10 days post-treatment day 1, calculated using the trapezoidal method, and comparing Anakinra to placebo treatment.
Day 1 of treatment through day 10 after treatment

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Effect of Anakinra on Asthma Index during moderate asthma exacerbation
Prazo: Day 1 of treatment to day 10 after treatment
Asthma Index is a continuous variable that reflects the magnitude and timing of changes in asthma control. Asthma scores are calculated using objective peak expiratory flow (PEF) and subjective symptom score elements over a 48-hour period. Asthma scores will be calculated over the period of treatment day 1 through 10 days post-treatment day 1 and subtracted from the mean Asthma score from a stable baseline 7-day period to obtain the Asthma Index. The area under the curve (AUC) of the Asthma Index will be calculated over the period of treatment day 1 through 10 days post-treatment day 1. Higher Asthma Index AUC values represent a greater cumulative burden of uncontrolled asthma relative to the individual's stable baseline (i.e., worse asthma control), while lower values represent better-maintained asthma control over the assessment period.
Day 1 of treatment to day 10 after treatment
Intervention Feasibility - Mean number of participants enrolled per month
Prazo: 18 months
Mean number of participants completing the screening visit and signing informed consent per month.
18 months
Intervention Feasibility - Mean number of participants randomized per month
Prazo: 18 months
Mean number of participants completing the training and randomization visit per month.
18 months
Intervention Feasibility - Percentage of participants retained through completion of study
Prazo: 24 months
Percentage of total randomized participants who complete visit 9 (end of study visit).
24 months
Study Design Feasibility - Percentage of participants completing daily PEF measurements
Prazo: 24 months
Percentage of randomized participants who complete at least 75% of expected daily PEF measurements.
24 months
Fidelity to Study Intervention - Percentage of prescribed doses of study treatment that are self-administered by the participant
Prazo: 24 months
Percentage of prescribed doses of study treatment that are completed through self-administration by the study participant during treatment visit 1 or treatment visit 2.
24 months
Percentage of participants requiring rescue systemic corticosteroid treatment
Prazo: The 10 day period following the start of treatment for an exacerbation
Among participants who experience an exacerbation event, the percentage who require treatment with systemic corticosteroids for ongoing symptoms and/or PEF reduction.
The 10 day period following the start of treatment for an exacerbation
Percentage of participants with rebound worsening of asthma exacerbation after study treatment
Prazo: The 10 day period following the start of treatment for an exacerbation
Among participants who experience an exacerbation event, the percentage who experience rebound worsening of the asthma exacerbation will be reported. Rebound worsening of asthma exacerbation is defined as an initial improvement in symptoms, short acting beta-agonist (SABA) use and/or peak expiratory flow (PEF) after study treatment with subsequent deterioration shown by a decline in PEF, increased SABA use, or need for systemic corticosteroids during Visits T4-T7.
The 10 day period following the start of treatment for an exacerbation
Percentage of participants experiencing an asthma exacerbation that requires emergency care
Prazo: The 10 day period following the start of treatment for an exacerbation
Among participants who experience an exacerbation event, the percentage who require emergency care, defined as an unscheduled primary care visit, urgent care visit, or emergency department visit, will be reported.
The 10 day period following the start of treatment for an exacerbation
Percentage of participants experiencing an asthma exacerbation that requires hospitalization.
Prazo: The 10 day period following the start of treatment for an exacerbation
Among participants who experience an exacerbation event, the percentage who require hospitalization will be reported
The 10 day period following the start of treatment for an exacerbation
Percentage of participants with post-treatment severe neutropenia.
Prazo: 14 days following the start of treatment for an exacerbation
Among participants who inject study treatment for an exacerbation, the percentage with post-treatment severe neutropenia will be reported. A post treatment complete blood count (CBC) will be performed and severe neutropenia will be defined as an absolute neutrophil count (ANC) < 500 cells/µL.
14 days following the start of treatment for an exacerbation
Percentage of participants experiencing serious infection
Prazo: The 14 day period following the start of treatment for an exacerbation
Among participants who inject study treatment for an exacerbation, the percentage who experience a serious infection (including pneumonia, cellulitis, kidney or neurologic infections, and bacteria or sepsis) will be reported.
The 14 day period following the start of treatment for an exacerbation
Percentage of participants experiencing an injection site reaction
Prazo: The 14 day period following the start of treatment for an exacerbation
Among participants who inject study treatment for an exacerbation, the percentage who experience injection site reactions will be reported.
The 14 day period following the start of treatment for an exacerbation
Percentage of accurately identified participants
Prazo: Up to 24 months
Electronic medical record (EMR)-based data pulls will occur at intervals throughout the enrollment period to identify potentially eligible participants through a computable phenotype. The percentage of potentially eligible participants that were accurately identified through this computable phenotype will be reported.
Up to 24 months

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Investigador principal: Michelle Hernandez, MD, University of North Carolina, Chapel Hill

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de novembro de 2026

Conclusão Primária (Estimado)

1 de janeiro de 2029

Conclusão do estudo (Estimado)

1 de janeiro de 2029

Datas de inscrição no estudo

Enviado pela primeira vez

6 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

14 de maio de 2026

Primeira postagem (Real)

20 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

15 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

13 de julho de 2026

Última verificação

1 de julho de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Descrição do plano IPD

Deidentified individual data that supports the results will be shared beginning 9 and continuing for 36 months following publication provided the investigator who proposes to use the data has approval from an Institutional Review Board (IRB), Independent Ethics Committee (IEC), or Research Ethics Board (REB), as applicable, and executes a data use/sharing agreement with UNC.

Prazo de Compartilhamento de IPD

9 and continuing for 36 months following publication.

Critérios de acesso de compartilhamento IPD

Investigators with approved IRB, IEC, or REB for use of the requested data and who have executed a data use/sharing agreement with UNC.

Tipo de informação de suporte de compartilhamento de IPD

  • PROTOCOLO DE ESTUDO
  • SEIVA
  • CIF

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Sim

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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