Tämä sivu käännettiin automaattisesti, eikä käännösten tarkkuutta voida taata. Katso englanninkielinen versio lähdetekstiä varten.

A Treatment Effectiveness Study Among SLE Patients Receiving Anifrolumab in Routine Clinical Practice. (ASTER)

maanantai 21. syyskuuta 2026 päivittänyt: AstraZeneca

ASTER: Anifrolumabitutkimus hoidon tehokkuudesta todellisessa maailmassa Monikansallinen, havainnollinen, lanseerauksen jälkeinen tehokkuustutkimus SLE-potilailla, jotka saavat anifrolumabia rutiinikliinisissä käytännöissä

Anifrolumab Study of Treatment Effectiveness in the Real World (ASTER) study will collect real world data to obtain a good understanding of the (sustained) clinical effect and patient quality of life outcomes among diagnosed SLE patients who initiate anifrolumab treatment. ASTER will generate critical real-world evidence on the benefits of adding anifrolumab to standard of care treatment for SLE in routine clinical practice, to inform physicians, payers and patients.

Tutkimuksen yleiskatsaus

Tila

Aktiivinen, ei rekrytointi

Ehdot

Interventio / Hoito

Yksityiskohtainen kuvaus

ASTER is a multi-country, single-arm, prospective, observational study. The study will be initiated on a country-by country basis following the commercial launch of anifrolumab. ASTER is a cohort study, with 1-year retrospective baseline data and up to 5 years of follow-up data.

The minimum enrolment period is anticipated to be 18 months (± 5 months) per country, but it may be extended, if necessary, to reach the overall study target.

In general, patients will enter the study between the first anifrolumab prescription and infusion (index), with follow-up until death, loss to follow-up, patient discontinuing the study, or end of study period (whichever occurs first). Data collection will continue for all patients including those who have discontinued anifrolumab during the study, unless the patients have withdrawn their consent for participation in the study. Relevant clinical data collection will continue for the entire follow up while patient reported outcome (PRO) data collection will continue only up to the 3-year follow up.

The study will use clinical assessments that are relevant for SLE-treating physicians in routine clinical practice, as well as introduce a specific measure for skin manifestations to affirm the potency of anifrolumab in treating SLE-related skin manifestations.

The eCRFs will be accessed through secure web-based portals and will be used to ensure consistent data collection for each healthcare provider involved in this study.

Electronic data collection will be the only method of data collection in this study.

Opintotyyppi

Havainnollistava

Ilmoittautuminen (Todellinen)

551

Yhteystiedot ja paikat

Tässä osiossa on tutkimuksen suorittajien yhteystiedot ja tiedot siitä, missä tämä tutkimus suoritetaan.

Opiskelupaikat

  • Belgia
      • Leuven, Belgia, 3000
        • Research Site
    • Li Ge
      • Liège, Li Ge, Belgia, 4000
        • Research Site
  • Israel
    • Central District
      • Kfar Saba, Central District, Israel, 4428164
        • Research Site
      • Tel Hashomer, Central District, Israel, 5211401
        • Research Site
    • Galilee
      • Tiberias, Galilee, Israel, 15208
        • Research Site
    • Haifa District
      • Haifa, Haifa District, Israel, 3109601
        • Research Site
      • Haifa, Haifa District, Israel, 3436212
        • Research Site
    • Jerusalem
      • Jerusalem, Jerusalem, Israel, 91120
        • Research Site
    • Northern District
      • Afula, Northern District, Israel, 18101
        • Research Site
    • Tel Aviv
      • Ramat Gan, Tel Aviv, Israel, 52621
        • Research Site
      • Tel Aviv, Tel Aviv, Israel, 6423906
        • Research Site
  • Italia
      • Ancona, Italia, 60126
        • Research Site
      • Bari, Italia, 70124
        • Research Site
      • Florence, Italia, 50134
        • Research Site
      • Milan, Italia, 20122
        • Research Site
      • Milan, Italia, 20132
        • Research Site
      • Pisa, Italia, 56126
        • Research Site
      • Roma, Italia, 168
        • Research Site
      • Roma, Italia, 161
        • Research Site
    • Campania
      • Naples, Campania, Italia, 80131
        • Research Site
    • Emilia-Romagna
      • Cona, Emilia-Romagna, Italia, 44124
        • Research Site
    • Friuli Venezia Giulia
      • Udine, Friuli Venezia Giulia, Italia, 33100
        • Research Site
    • Lazio
      • Rome, Lazio, Italia, 149
        • Research Site
    • Lombardy
      • Brescia, Lombardy, Italia, 25100
        • Research Site
      • Milan, Lombardy, Italia, 20122
        • Research Site
    • Piedmont
      • Turin, Piedmont, Italia, 10126
        • Research Site
    • Sardinia
      • Cagliari, Sardinia, Italia, 9042
        • Research Site
  • Itävalta
      • Vienna, Itävalta, 1180
        • Research Site
    • Tyrol
      • Innsbruck, Tyrol, Itävalta, 6020
        • Research Site
    • Upper Austria
      • Linz, Upper Austria, Itävalta, 4020
        • Research Site
  • Kanada
    • Alberta
      • Calgary, Alberta, Kanada, T2N 4N1
        • Research Site
    • Manitoba
      • Winnipeg, Manitoba, Kanada, RR149
        • Research Site
    • Ontario
      • Hamilton, Ontario, Kanada, L8N 3Z5
        • Research Site
      • Orillia, Ontario, Kanada, L3V 1T5
        • Research Site
      • Toronto, Ontario, Kanada, M5T 2S9
        • Research Site
    • Quebec
      • Rimouski, Quebec, Kanada, G5L 5T1
        • Research Site
      • Sherbrooke, Quebec, Kanada, J1G 2E8
        • Research Site
      • Ste-Foy, Quebec, Kanada, G1V 4G2
        • Research Site
  • Ranska
      • Paris, Ranska, 75020
        • Research Site
      • Paris, Ranska, 75014
        • Research Site
      • Paris, Ranska, 75013
        • Research Site
      • Paris, Ranska, 75475
        • Research Site
      • Paris, Ranska, 14033
        • Research Site
    • Alpes-Maritimes
      • Nice, Alpes-Maritimes, Ranska, 6000
        • Research Site
    • Auvergne-Rh ne-Alpes
      • Clermont-Ferrand, Auvergne-Rh ne-Alpes, Ranska, 63000
        • Research Site
    • Bas-Rhin
      • Strasbourg, Bas-Rhin, Ranska, 67098
        • Research Site
    • Brest Cedex
      • Finist Re, Brest Cedex, Ranska, 29609
        • Research Site
    • C te-d'Or
      • Dijon, C te-d'Or, Ranska, 21079
        • Research Site
    • Gironde
      • Bordeaux, Gironde, Ranska, 33076
        • Research Site
    • Is Re
      • Grenoble, Is Re, Ranska, 38043
        • Research Site
    • La R Union
      • Saint-Denis, La R Union, Ranska, 97405
        • Research Site
    • Loire-Atlantique
      • Nantes, Loire-Atlantique, Ranska, 44093
        • Research Site
    • Lyon
      • Bouches-du-Rh Ne, Lyon, Ranska, 69003
        • Research Site
    • Martinique
      • FORT de France Cedex, Martinique, Ranska, 97261
        • Research Site
    • Nord
      • Lille, Nord, Ranska, 59037
        • Research Site
    • Rouen
      • Seine-Maritime, Rouen, Ranska, 76230
        • Research Site
  • Ruotsi
    • N Rke
      • Örebro, N Rke, Ruotsi, 70185
        • Research Site
    • Uppland
      • Stockholm, Uppland, Ruotsi, 171 76
        • Research Site
  • Saksa
      • Berlin, Saksa, 10117
        • Research Site
    • Baden-W Rttemberg
      • Heidelberg, Baden-W Rttemberg, Saksa, 69120
        • Research Site
    • Baden-Wurttemberg
      • Heidelberg, Baden-Wurttemberg, Saksa, 69120
        • Research Site
    • Bavaria
      • Erlangen, Bavaria, Saksa, 91054
        • Research Site
    • Free and Hanseatic City of Hamburg
      • Bad Bramstedt, Free and Hanseatic City of Hamburg, Saksa, 24576
        • Research Site
    • L Beck
      • Schleswig-Holstein, L Beck, Saksa, 23562
        • Research Site
    • Mecklenburg-Vorpommern
      • Greifswald, Mecklenburg-Vorpommern, Saksa, 17493
        • Research Site
    • North Rhine-Westphalia
      • Cologne, North Rhine-Westphalia, Saksa, 51149
        • Research Site
      • D Sseldorf, North Rhine-Westphalia, Saksa, 40225
        • Research Site
      • Herne, North Rhine-Westphalia, Saksa, 44649
        • Research Site
    • Rhineland-Palatinate
      • Mainz A. Rhein, Rhineland-Palatinate, Saksa, 55131
        • Research Site
    • Saxony-Anhalt
      • Magdeburg, Saxony-Anhalt, Saksa, 39104
        • Research Site
    • Vorpommern-Greifswald
      • Greifwald, Vorpommern-Greifswald, Saksa, 17489
        • Research Site
  • Yhdistyneet Arabiemiirikunnat
      • Abu Dhabi, Yhdistyneet Arabiemiirikunnat
        • Research Site
    • Dubayy
      • Dubai, Dubayy, Yhdistyneet Arabiemiirikunnat, 7272
        • Research Site
    • Emirate of Sharjah
      • Sharjah city, Emirate of Sharjah, Yhdistyneet Arabiemiirikunnat, 72772
        • Research Site

Osallistumiskriteerit

Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.

Kelpoisuusvaatimukset

Opintokelpoiset iät

18 vuotta - 130 vuotta (Aikuinen, Vanhempi Aikuinen)

Hyväksyy terveitä vapaaehtoisia

Ei

Sukupuolet, jotka voivat opiskella

Kaikki

Näytteenottomenetelmä

Ei-todennäköisyysnäyte

Tutkimusväestö

All patients aged ≥18 years diagnosed with SLE who initiate anifrolumab as prescribed by their healthcare provider (HCP) per the approved country-specific label and are treated at the study sites will be eligible for inclusion.

Kuvaus

Inclusion Criteria:

  • Fulfilled the 2019 EULAR (European League Against Rheumatism)/ACR (American College of Rheumatology) criteria for SLE at the time of study entry.
  • Prescribed anifrolumab for their SLE treatment for the first time, according to approved country-specific label.
  • The Physician's decision to prescribe anifrolumab must occur prior to any study-related discussion.
  • In countries where prescription reimbursements are authorised on a case-by-case basis, authorisation (ie, patient access to treatment) will be required for study entry.

Exclusion Criteria:

  • Currently participating in an anifrolumab early access/compassionate use program or an interventional clinical trial with an investigational product.
  • Any previous exposure to anifrolumab (including as part of a clinical trial or early access programme).
  • Documented diagnosis of severe or rapidly progressive Class III or IV glomerulonephritis requiring induction therapy (mycophenolate mofetil [MMF]/cyclophosphamide [CYC] + high dose steroids), isolated Class V lupus nephritis (in absence of other SLE manifestations, ie. skin/joint involvement), or active severe or unstable neuropsychiatric lupus.
  • Any other condition which the investigator deems to limit a patient's ability to understand the informed consent.

Opintosuunnitelma

Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.

Miten tutkimus on suunniteltu?

Suunnittelun yksityiskohdat

  • Havaintomallit: COHORT
  • Aikanäkymät: PROSPECTIVE

Kohortit ja interventiot

Ryhmä/Kohortti
Interventio / Hoito
Prospective Cohort

All patients aged ≥18 years diagnosed with SLE who initiate anifrolumab as prescribed by their healthcare provider (HCP) per the approved country-specific label and are treated at the study sites will be eligible for inclusion.
Muut: None (Observational study)

Not Applicable since Observational Study

Muut nimet:
  • Havaintotutkimus

Mitä tutkimuksessa mitataan?

Ensisijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Disease activity assessed by the Physician Global Assessment (PGA)
Aikaikkuna: From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation

The PGA is a single-item visual analogue scale that describes the physician assessment of a patient's disease and its impact on daily functioning at the time of assessment. The scale ranges from 0 (asymptomatic disease and no limitation of normal activities) to 3 (severe disease and limitation of normal activities).
From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation
Disease activity assessed by Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K)
Aikaikkuna: From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation

The SLEDAI-2K is a global index and includes 24 clinical symptoms and laboratory variables that are weighted by the type of manifestation, but not by severity or dynamic of the individual item. The SLEDAI-2K includes scoring for antibodies and low complement, as well as some renal and hematologic parameters. The total score ranges between 0 and 105, with higher scores representing increased disease activity.
From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation
Proportion of patients attaining the composite endpoint of lupus low disease activity (LLDAS)
Aikaikkuna: From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation

The proportion of patients attaining the composite endpoint of LLDAS will be assesed.
From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation

Toissijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Proportion of patients attaining Definition of Remission in SLE (DORIS)
Aikaikkuna: From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation

The proportion of patients attaining the Definition of Remission in SLE will be assesed.
From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation
Clinical SLE Flares assessment by modified revised Safety of Estrogens in Lupus National Assessment-Systemic Lupus Erythematosus Disease Activity Index (SELENA-SLEDAI) flare index (rSFI)
Aikaikkuna: From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation

Flare will be defined as any one criterion present either the Mild/Moderate Flare or Severe Flare categories. New or worsened manifestation will only be reported for manifestation of SLE.
From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation
Proportion of patients with irreversible organ damage, using the Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index (SDI).
Aikaikkuna: From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation

The proportion of patients with irreversible organ damage, using the Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index will be assessed. The irreversible, accumulated organ damage from either the disease process or disease treatment, which has been present for at least 6 months, in 12 organ systems will be measured.
From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation
SLE treatment patterns prior to, concomitant with and after anifrolumab
Aikaikkuna: From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation

SLE treatment patterns will be analyzed through prevalence and incidence in respect to time to discontinuation.
From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation
Functional Assessment of Chronic Illness Therapy - Fatigue Scale (FACIT-Fatigue)
Aikaikkuna: From Baseline (1 year pre-anifrolumab) until follow-up 3 years post-anifrolumab initiation

The FACIT-Fatigue is a 13-item questionnaire formatted for self-administration that assesses patient-reported fatigue and its impact upon daily activities and function over the past 7 days. Patients will be asked to answer each question using a 5-point verbal rating scale, with total scores ranging from 0 (most fatigued) to 52 (least fatigued).
From Baseline (1 year pre-anifrolumab) until follow-up 3 years post-anifrolumab initiation
Lupus Quality of Life (LupusQoL)
Aikaikkuna: From Baseline (1 year pre-anifrolumab) until follow-up 3 years post-anifrolumab initiation

The LupusQoL is a validated SLE-specific HRQoL (health-related quality of life) instrument consisting of 34 items across 8 domains (Physical health, Emotional health, Body image, Pain, Planning, Fatigue, Intimate relationships, and Burden to others). The LupusQoL has a 5-point verbal rating scale, and uses a 4-week recall period. The mean raw domain score is transformed to scores ranging from 25 (worst HRQoL) to 125 (best HRQoL) by dividing by 4 and then multiplying by 100.
From Baseline (1 year pre-anifrolumab) until follow-up 3 years post-anifrolumab initiation
Patient Global Assessment (PtGA)
Aikaikkuna: From Baseline (1 year pre-anifrolumab) until follow-up 3 years post-anifrolumab initiation

The PtGA is a single-item question that takes into account all the ways in which illness and health conditions may affect the patient at this time. The patient should consider the previous week when answering this question. Responses range from 0 (Very Well) to 100 (Very Poorly) on a visual analogue scale (VAS).
From Baseline (1 year pre-anifrolumab) until follow-up 3 years post-anifrolumab initiation
EuroQol 5-Dimension Health Questionnaire 5 Level (EQ-5D-5L)
Aikaikkuna: From Baseline (1 year pre-anifrolumab) until follow-up 3 years post-anifrolumab initiation

The EQ-5D-5L is a general health status measure comprising a descriptive system and the EQ VAS. The descriptive system comprises 5 dimensions: Mobility, Self-care, Usual activities, Pain/discomfort and Anxiety/depression. Patients are asked to rate their current health and functional status on a 5-point verbal rating scale for each of the 5 domains. Responses are converted into an overall quality of life score via a preference-based statistical mapping algorithm. The scores on these 5 dimensions can be presented as a health profile or can be converted to a single summary index number (utility) reflecting preferability compared to other health profiles. Additionally, patients are asked to indicate how they rate their current overall health on a visual analog scale (EQ-VAS) ranges from 100 for best imaginable health state to 0 for worst imaginable health state.
From Baseline (1 year pre-anifrolumab) until follow-up 3 years post-anifrolumab initiation
Work Productivity and Activity Impairment - Lupus (WPAI:lupus)
Aikaikkuna: From Baseline (1 year pre-anifrolumab) until follow-up 3 years post-anifrolumab initiation

The WPAI:Lupus is an SLE-specific, self-administered questionnaire, that assesses the impact of disease on productivity. The WPAI:Lupus consists of 6 items and has a recall period of the past 7 days. The WPAI:Lupus is divided into 4 domains: Absenteeism (work time missed), Presenteeism (VAS [scored from 0 to 10] rating of impairment while working), Working Productivity Loss (overall work impairment/absenteeism plus presenteeism), and Activity Impairment (VAS [scored from 0 to 10] rating of daily activity, other than work at a job). Scores for each domain are expressed as impairment percentages, with higher scores indicating greater productivity impairment.
From Baseline (1 year pre-anifrolumab) until follow-up 3 years post-anifrolumab initiation
Pain Numerical Rating Scale (NRS)
Aikaikkuna: From Baseline (1 year pre-anifrolumab) until follow-up 3 years post-anifrolumab initiation

The pain NRS will measure the pain severity in the past seven days on a scale of 0-10 (0: no pain; 10: worst pain imaginable).
From Baseline (1 year pre-anifrolumab) until follow-up 3 years post-anifrolumab initiation
Number of outpatient hospital and emergency room visits and procedures
Aikaikkuna: From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation

The healthcare resource utilisation (HCRU) for SLE after anifrolumab initiation as recorded in medical records will be assessed. The number of outpatient hospital and emergency room visits and procedures.
From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation
Number of hospital admissions and inpatient hospital procedures
Aikaikkuna: From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation

The HCRU for SLE after anifrolumab initiation as recorded in medical records will be assessed. The number of hospital admissions and inpatient hospital procedures (including duration of hospital stay and reason for hospitalization, stratified by admission to an intensive care unit [ICU] vs non-ICU) will be assessed.
From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation
Number of rheumatologist visits and procedures
Aikaikkuna: From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation

The HCRU for SLE after anifrolumab initiation as recorded in medical records will be assessed. The number of rheumatologist visits and procedures (including SLE-related laboratory tests) will be assessed.
From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation
Number of dialysis appointments
Aikaikkuna: From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation

The HCRU for SLE after anifrolumab initiation as recorded in medical records will be assessed. The number of dialysis appointments will be assessed.
From Baseline (1 year pre-anifrolumab) until follow-up 5 years post-anifrolumab initiation

Yhteistyökumppanit ja tutkijat

Täältä löydät tähän tutkimukseen osallistuvat ihmiset ja organisaatiot.

Sponsori

AstraZeneca

Yhteistyökumppanit

Parexel

Julkaisuja ja hyödyllisiä linkkejä

Tutkimusta koskevien tietojen syöttämisestä vastaava henkilö toimittaa nämä julkaisut vapaaehtoisesti. Nämä voivat koskea mitä tahansa tutkimukseen liittyvää.

Yleiset julkaisut

Opintojen ennätyspäivät

Nämä päivämäärät seuraavat ClinicalTrials.gov-sivustolle lähetettyjen tutkimustietueiden ja yhteenvetojen edistymistä. National Library of Medicine (NLM) tarkistaa tutkimustiedot ja raportoidut tulokset varmistaakseen, että ne täyttävät tietyt laadunvalvontastandardit, ennen kuin ne julkaistaan ​​julkisella verkkosivustolla.

Opi tärkeimmät päivämäärät

Opiskelun aloitus (Todellinen)

Maanantai 27. helmikuuta 2023

Ensisijainen valmistuminen (Arvioitu)

Maanantai 30. joulukuuta 2030

Opintojen valmistuminen (Arvioitu)

Maanantai 30. joulukuuta 2030

Opintoihin ilmoittautumispäivät

Ensimmäinen lähetetty

Torstai 24. marraskuuta 2022

Ensimmäinen toimitettu, joka täytti QC-kriteerit

Torstai 24. marraskuuta 2022

Ensimmäinen Lähetetty (Todellinen)

Maanantai 5. joulukuuta 2022

Tutkimustietojen päivitykset

Viimeisin päivitys julkaistu (Todellinen)

Torstai 24. syyskuuta 2026

Viimeisin lähetetty päivitys, joka täytti QC-kriteerit

Maanantai 21. syyskuuta 2026

Viimeksi vahvistettu

Tiistai 1. syyskuuta 2026

Lisää tietoa

Tähän tutkimukseen liittyvät termit

Avainsanat

Muita asiaankuuluvia MeSH-ehtoja

Muut tutkimustunnusnumerot

  • D3461R00043

Yksittäisten osallistujien tietojen suunnitelma (IPD)

Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?

JOO

IPD-suunnitelman kuvaus

Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca group of companies sponsored clinical trials via the request portal. All request 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.

IPD-jaon aikakehys

AstraZeneca will meet or exceed data availability as per the commitments made to the EFPIA Pharma Data Sharing Principles. For details of our timelines, please rerefer to our disclosure commitment at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.

IPD-jaon käyttöoikeuskriteerit

When a request has been approved AstraZeneca will provide access to the deidentified individual patient-level data in an approved sponsored tool. Signed Data Sharing Agreement (non-negotiable contract for data accessors) must be in place before accessing requested information. Additionally, all users will need to accept the terms and conditions of the SAS MSE to gain access. For additional details, please review the Disclosure Statements at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.

Lääke- ja laitetiedot, tutkimusasiakirjat

Tutkii yhdysvaltalaista FDA sääntelemää lääkevalmistetta

Ei

Tutkii yhdysvaltalaista FDA sääntelemää laitetuotetta

Ei

Nämä tiedot haettiin suoraan verkkosivustolta clinicaltrials.gov ilman muutoksia. Jos sinulla on pyyntöjä muuttaa, poistaa tai päivittää tutkimustietojasi, ota yhteyttä register@clinicaltrials.gov. Heti kun muutos on otettu käyttöön osoitteessa clinicaltrials.gov, se päivitetään automaattisesti myös verkkosivustollemme .

Tilaa