Resumen

El objetivo de este estudio es evaluar el potencial de los pacientes tratados con tezepelumab (administración subcutánea) para reducir el tratamiento de mantenimiento sin pérdida del control del asma en adolescentes y adultos con asma grave. Los detalles del estudio incluyen: 1. La duración del estudio será de hasta 72 semanas. 2. La duración del tratamiento será de hasta 68 semanas. 3. La frecuencia de visitas será una vez cada 4 semanas (Q4W).

Descripción detallada

Se trata de un estudio multicéntrico, aleatorizado, abierto, de grupos paralelos y de fase IIIb para evaluar el potencial de los pacientes tratados con tezepelumab para (1) reducir el tratamiento de mantenimiento sin pérdida del control del asma en la Semana 56, entre aquellos que demostraron control del asma o biomarcadores bajos en la Semana 24, y (2) tener control del asma y presentar características de remisión clínica en la Semana 24. Aproximadamente 65 centros en 10 países incluirán pacientes adultos y adolescentes con asma grave no controlada. El estudio se divide en 5 fases tal como se describe a continuación: * Fase de cribado/rodaje (desde la Semana -4 hasta la Semana 0, hasta 4 semanas) * Fase de inducción del tratamiento (Semana 0 a Semana 4) * Fase de continuación del tratamiento (Semana 4 a Semana 24) * Fase de tratamiento con tezepelumab con o sin terapia de reducción de dosis de ICS (Semana 24 a Semana 56) * Fase de mantenimiento (Semana 56 a Semana 72)

Elegibilidad

Edad mínima: 12 YearsEdad máxima: 80 YearsSexo: ALL

Criterios de inclusión

Informed Consent
Provision of signed and dated written ICF prior to any mandatory study-specific procedures, sampling, and analyses for patients who are at or over the age of majority (as per local law). For patients who are less than the age of majority, in addition to providing their informed consent, the patients' legally authorised representative must also provide their informed assent (Appendix A 3).
Age
Patients must be 12 to 80 years of age inclusive, at the time of signing the ICF.
Type of Patient and Disease Characteristics
Documented medical record history for at least 12 months prior to Visit 1.
Documented physician-diagnosed severe asthma within 10 years prior to Visit 1 (ie, severe asthma was not diagnosed more than 10 years prior) consisting of any of the following:
FEV1 \> 12% reversibility, OR
Evidence of airflow variability (to show that lung function is altered over time): FEV1 ≥ 400 mL variability over time, OR
Challenge tests that are positive on one of the below:
(i) Methacholine - PD20 ≤ 8 mg/mL (ii) Mannitol - PD15 15% drop on FEV1 out of dose \< than 635 mg of inhaled mannitol (iii) Exercise - 10% fall of FEV1
ACQ-5 ≥ 1.5 and \< 3.
History of physician-diagnosed asthma that requires continuous treatment with high-dose ICS (as defined by GINA or highest approved dose per posology per country) plus a LABA for at least 6 months prior to Visit 1 (Appendix I). The ICS and LABA can be contained within a combination product or given by separate inhalers.
Note: Additional maintenance asthma controller medications (eg, LTRAs, tiotropium, cromone, theophylline) are allowed.
Pre-brochodilator FEV1 \> 60% predicted and evidence of FEV1 reversibility of \> 12% within 6 months prior to screening or at screening. Patients with normal lung function (FEV1 \> 80%) need evidence of airflow variability as per inclusion criterion 4.
Documented history of at least one asthma exacerbation requiring OCS bursts or requiring hospitalization within 12 months prior to Visit 1. An asthma exacerbation will be defined as a worsening of asthma symptoms that leads to any of the following:
A temporary bolus/burst of systemic corticosteroids for at least 3 consecutive days to treat symptoms of asthma worsening; a single depo-injectable dose of corticosteroids will be considered equivalent to a 3-day bolus/burst of systemic corticosteroids
Or, an ER visit (defined as evaluation and treatment for \< 24 hours in ER) due to asthma that required systemic corticosteroids (as per above)
Or, an in-patient hospitalisation (defined as admission to an inpatient facility and/or evaluation and treatment in a healthcare facility for ≥ 24 hours).
Sex and Contraceptive/Barrier Requirements
Male or female.
Female patients:
Contraceptive use by women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies. Women of nonchildbearing potential are defined as women who are either permanently sterilised (hysterectomy, bilateral oophorectomy, or bilateral salpingectomy) or who are postmenopausal. Women will be considered postmenopausal if they have been amenorrhoeic for 12 months prior to the planned start date of the induction phase without an alternative medical cause.
The following age-specific requirements apply:
Women \< 50 years old would be considered postmenopausal if they have been amenorrhoeic for 12 months or more following cessation of exogenous hormonal treatment and follicle-stimulating hormone levels in the postmenopausal range.
Women ≥ 50 years old would be considered postmenopausal if they have been amenorrhoeic for 12 months or more following cessation of all exogenous hormonal treatment.
Adolescents: if patient is female and has reached menarche or has reached Tanner stage 3 breast development (even if not having reached menarche), the patient will be considered a WOCBP.
WOCBP must be willing to use one of the methods of contraception described hereafter, from the time of signing the ICF throughout the study and 16 weeks after last tezepelumab administration:
Combined (oestrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation: oral, intravaginal, transdermal
Progestogen-only hormonal contraception associated with inhibition of ovulation: oral, injectable, implantable
Intrauterine device
Intrauterine hormone-releasing system
Bilateral tubal occlusion
Vasectomised partner (vasectomised partner is a highly effective birth control method provided that the partner is the sole sexual partner of the WOCBP patient and that the vasectomised partner has received medical assessment of the surgical success)
Sexual abstinence: it is considered a highly effective method only if defined as refraining from heterosexual intercourse during the entire period of risk associated with the study treatments. The reliability of sexual abstinence needs to be evaluated in relation to the duration of the study and the preferred and usual lifestyle of the patient.
Cessation of contraception after this point should be discussed with a responsible physician
Before dosing with tezepelumab at Week 0, patients should fulfil the following criteria:
ACQ-5 ≥ 1.5 and \< 3.
Demonstrated proper inhaler technique (patients with improper technique at screening may be trained during screening, but must demonstrate proper technique before enrollment).
No excessive SABA use (should be \< 5 puffs/day) or for patients using SMART therapy outside the US, no excessive use of SYMBICORT (should be ≤ 8 inhalations/day) or for US patients, no excessive use of AIRSUPRA (should be ≤ 12 inhalations/day).

Criterios de exclusión

Medical Conditions
Any clinically important pulmonary disease other than asthma (eg, active lung infection, chronic obstructive pulmonary disease, bronchiectasis, pulmonary fibrosis, cystic fibrosis, hypoventilation syndrome associated with obesity, lung cancer, alpha 1 anti-trypsin deficiency, and primary ciliary dyskinesia) or pulmonary or systemic diseases, other than asthma, that are associated with elevated peripheral EOS counts (eg, allergic bronchopulmonary aspergillosis/mycosis, Churg-Strauss syndrome, hypereosinophilic syndrome).
Any disorder, including, but not limited to, cardiovascular, gastrointestinal, hepatic, renal, neurological, musculoskeletal, infectious, endocrine, metabolic, haematological, psychiatric, or major physical impairment that is not stable in the opinion of the investigator and could:
Affect the safety of the patient throughout the study
Influence the findings of the study or the interpretation
Impede the patient's ability to complete the entire duration of study.
A helminth parasitic infection diagnosed within 6 months prior to Visit 1 that has not been treated with, or has failed to respond to, standard of care therapy.
Current smokers or patients with smoking history ≥ 10 pack-years and patients using vaping products, including electronic cigarettes. Former smokers with a smoking history of \< 10 pack-years and users of vaping or e-cigarette products must have stopped for at least 6 months prior to Visit 1 to be eligible.
History of chronic alcohol or drug abuse within 12 months prior to Visit 1.
Tuberculosis requiring treatment within the 12 months prior to Visit 1.
History of known immunodeficiency disorder including a positive human immunodeficiency virus test at Visit 1, or the patient taking antiretroviral medications as determined by medical history and/or patient's verbal report.
Major surgery within 8 weeks prior to Visit 1 or planned surgical procedures requiring general anaesthesia or inpatient status for \> 1 day during the conduct of the study.
Evidence of COVID-19 within 4 weeks prior to screening or ongoing clinically significant COVID-19 sequelae.
Prior/Concomitant Therapy
Receipt of any marketed or investigational biologic agent within 4 months or 5 half-lives (whichever is longer) prior to Visit 1 or receipt of any investigational nonbiologic agent within 30 days or 5 half-lives (whichever is longest) prior to Visit 1.
OCS-dependent patients (received chronic OCS therapy \[prednisone ≥ 5 mg/day or equivalent\]) for at least 3 months preceding Visit 1.
Daily use of maintenance corticosteroids for any reason.
Treatment with systemic immunosuppressive/immunomodulating drugs (eg, methotrexate, cyclosporine, etc.), except for OCS used in the treatment of asthma/asthma exacerbations, within the last 12 weeks or 5 half-lives (whichever is longer) prior to Visit 1.
Receipt of immunoglobulin or blood products within 30 days prior to Visit 1.
Receipt of live attenuated vaccines 30 days prior to the date of Visit 1 and during the study.
Patients that have been treated with bronchial thermoplasty in the last 12 months prior to Visit 1.
Prior/Concurrent Clinical Study Experience
Known history of sensitivity to any component of the tezepelumab formulation or a history of drug or other allergy that, in the opinion of the investigator or medical monitor, contraindicates their participation.
History of anaphylaxis or documented immune complex disease (Type III hypersensitivity reactions) following any biologic therapy.
Concurrent enrolment in another clinical study involving an IMP.
Diagnostic Assessments
Any clinically meaningful abnormal finding in physical examination, haematology, clinical chemistry at Visit 1 which, in the opinion of the investigator, may put the patient at risk because of his/her participation in the study, or may influence the results of the study, or the patient's ability to complete the entire duration of the study.
Evidence of active liver disease, including jaundice or AST, ALT, or ALP \> 2 times the ULN at Visit 1.
Positive hepatitis B surface antigen, hepatitis C virus antibody serology at screening, or a positive medical history for hepatitis B or C. Patients with a history of hepatitis B vaccination without a history of hepatitis B are allowed to participate.
Other Exclusions
Involvement in the planning and/or conduct of the study (applies to AstraZeneca staff and/or site staff), or patients employed by or relatives of the employees of the site or AstraZeneca.
Judgement by the investigator that the patient should not participate in the study if the patient is unlikely to comply with study procedures, restrictions, and requirements.
For women only: Pregnant, breastfeeding, or lactating women. A serum β-HCG pregnancy test must be drawn for WOCBP at the screening visit. If the results of the serum β-HCG cannot be obtained prior to dosing of the IMP, a patient may be enrolled on the basis of a negative urine pregnancy test, though serum β-HCG must still be obtained. If either test is positive, the patient should be excluded. Since urine and serum tests may miss a pregnancy in the first days after conception, relevant menstrual history and sexual history, including methods of contraception, should be considered. Any patient whose menstrual and/or sexual history suggests the possibility of early pregnancy should be excluded.

Intervenciones

combination_product

Tezepelumab

IMP. Subcutaneous injection. Unit dose strengths 210 mg.

combination_product

Budesonide/formoterol

AxMP. Oral inhalation. High-dose: 160 μg/4.5 μg per inhalation; Medium and Low-dose: 80 μg/4.5 μg per inhalation

combination_product

Albuterol/budesonide (AIRSUPRA®)

AxMP. Oral inhalation. Reliever only. Unit dose strengths 90 μg/80 μg per inhalation In US only.

combination_product

Mannitol

NIMP. Oral nebulization. Unit dose strengths: Graduated doses of 0 mg, 5 mg, 10 mg, 20 mg and 40 mg capsules

combination_product

Salbutamol

AxMP. Used outside the US only. Oral inhalation. Unit dose strengths: 100 μg per inhalation

Ubicaciones

Research Site

Berazategui, Argentina

Research Site

CABA, Argentina

Research Site

Concepción del Uruguay, Argentina

Research Site

Mendoza, Argentina

Research Site

Mendoza, Argentina

Research Site

Quilmes, Argentina

Research Site

Rosario, Argentina

Research Site

Rosario, Argentina

Research Site

San Miguel de Tucumán, Argentina

Research Site

Santa Fe, Argentina

Estudio multicéntrico, aleatorizado, abierto, de grupos paralelos y de fase IIIb para evaluar el potencial de los pacientes tratados con tezepelumab con asma grave para reducir el tratamiento de fondo manteniendo el control del asma y la remisión clínica

Resumen

Descripción detallada

Elegibilidad

Criterios de inclusión

Criterios de exclusión

Intervenciones

Tezepelumab

Budesonide/formoterol

Albuterol/budesonide (AIRSUPRA®)

Mannitol

Salbutamol

Ubicaciones

Research Site

Research Site

Research Site

Research Site

Research Site

Research Site

Research Site

Research Site

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Research Site

Patrocinadores