- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT07600190
Anakinra Rescue Treatment for Moderate Asthma Attacks (ARTMA) (ARTMA)
Anakinra Rescue Treatment for Moderate Asthma Attacks (ARTMA) Pilot Study
Studie Overzicht
Toestand
Interventie / Behandeling
Gedetailleerde beschrijving
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.
Studietype
Inschrijving (Geschat)
Fase
- Fase 1
Contacten en locaties
Studiecontact
- Naam: Chris Brooks
- Telefoonnummer: 919-843-6598
- E-mail: chris_brooks@med.unc.edu
Studie Contact Back-up
- Naam: Corinne Taylor
- Telefoonnummer: 919-962-9841
- E-mail: corinne.lawler@unc.edu
Studie Locaties
-
-
North Carolina
-
Chapel Hill, North Carolina, Verenigde Staten, 27599
- University of North Carolina Chapel Hill
-
Hoofdonderzoeker:
- Michelle Hernandez, MD
-
Contact:
- Corinne Taylor
- Telefoonnummer: 919-962-9841
- E-mail: corinne.lawler@unc.edu
-
Contact:
- Chris Brooks
- Telefoonnummer: (919) 843-6598
- E-mail: Chris_Brooks@med.unc.edu
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Beschrijving
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:
- 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.
- History of undergoing bronchial thermoplasty.
- Intubation for asthma in the last 12 months
- History of malignancy except non-melanoma skin cancer within the last five years.
- 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.
- 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.
- 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.
- Allergy/sensitivity to study drugs or their formulations, including latex
- Unwillingness to use reliable contraception if sexually active (IUD, birth control pills/patch, condoms).
- 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:
- Use of daily systemic corticosteroid therapy for asthma control
- Use of any immunomodulatory therapy within the preceding 12 months, including biologics that are approved for asthma.
- Currently receiving allergen immunotherapy
- 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:
- Positive QuantiFERON-tuberculosis (TB) gold assay. Cases of indeterminate QuantiFERON-TB test results will require a second specimen to be drawn.
- 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).
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Verviervoudigen
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Actieve vergelijker: Active Treatment
Subjects will be randomized to receive two doses of active study treatment (anakinra) upon meeting orange zone exacerbation criteria.
|
Active study treatment
|
|
Placebo-vergelijker: Placebo
Subjects will be randomized to receive two doses of placebo upon meeting orange zone exacerbation criteria.
|
Placebo
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Study Design Feasibility - Percentage of participants who experience one moderate asthma exacerbation
Tijdsspanne: 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
Tijdsspanne: 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
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Effect of Anakinra on Asthma Index during moderate asthma exacerbation
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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.
Tijdsspanne: 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.
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
|
Medewerkers en onderzoekers
Onderzoekers
- Hoofdonderzoeker: Michelle Hernandez, MD, University of North Carolina, Chapel Hill
Studie record data
Bestudeer belangrijke data
Studie start (Geschat)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Pathologische processen
- Ziekten van het immuunsysteem
- Ziekten van de luchtwegen
- Longziekten
- Bronchiale ziekten
- Longziekten, obstructief
- Ademhalingsovergevoeligheid
- Overgevoeligheid, Onmiddellijk
- Overgevoeligheid
- Pathologische aandoeningen, tekenen en symptomen
- Astma
- Ziekte
- Peptiden
- Aminozuren, peptiden en eiwitten
- Eiwitten
- Biologische factoren
- Intercellulaire signaalpeptiden en eiwitten
- Cytokines
- Interleukine 1-receptorantagonisteiwit
Andere studie-ID-nummers
- 25-1995
- R34HL179910 (Subsidie/contract van de Amerikaanse NIH)
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
IPD-tijdsbestek voor delen
IPD-toegangscriteria voor delen
IPD delen Ondersteunend informatietype
- LEERPROTOCOOL
- SAP
- ICF
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .