Asthma Trial, Recruiting NCT06422078 Sponsor: AstraZeneca Condition: Asthma
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Asthma Trial, Recruiting

NCT06422078
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults aged 18 or older, of any gender
  • People with a confirmed diagnosis of severe eosinophilic asthma (a type of asthma involving high levels of certain immune cells), as defined by major respiratory medical guidelines, who are already being treated with high-dose inhaled steroids plus a long-acting bronchodilator
  • People for whom a doctor has already prescribed benralizumab (a biologic asthma medication) based on standard prescribing and reimbursement criteria — the treatment decision must have been made before and separately from this study
  • People who are able and willing to read and understand written instructions
  • People who have signed a consent form showing they understand the study's purpose and procedures and agree to take part
  • People who are willing to report on their asthma symptoms every 4 weeks and record their medication use weekly

Who may not be able to join:

  • People currently taking part in another observational study that the trial investigators believe could affect this study's results, or who took part in a randomised clinical trial within the last 3 months
  • People with a history of a severe allergic reaction (anaphylaxis) to any biologic medication
  • People who have received any biologic therapy for asthma within the last 3 months
  • People currently using any other biologic therapy for asthma at the same time
  • People diagnosed with a parasitic worm (helminth) infection within the past 24 weeks that has not been successfully treated
  • People with a lung condition other than asthma that, in the investigator's view, could affect how the study results are interpreted
  • People with any ongoing or long-term condition that, in the investigator's view, could limit their ability to complete questionnaires or participate fully in the study
  • People with a history of cancer within the last 5 years — with two exceptions: cervical carcinoma in situ where treatment is complete and the person has been in remission for at least 12 months, or certain minor skin cancers (basal cell carcinoma or superficial squamous cell skin cancer)
  • People who are pregnant or breastfeeding (the investigator is required to ask about this)
  • People with any other condition that, in the investigator's opinion, could put their safety at risk

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 1-877-240-9479

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Registry
ClinicalTrials.gov
Start date
25 July 2024
Est. completion
31 December 2027

Where this trial is recruiting

🇩🇪 Germany

Primary endpoints

Change in Asthma Control Test (ACT) total score in patients from baseline to week 12, 24 and 52 after first benralizumab dose; Proportion of responders at baseline, week 12, 24 and 52 after first benralizumab dose, using ACT; Change in daily doses of prescribed inhaled corticosteroids (ICS) intake from baseline to week 12, 24 and 52 after first benralizumab dose; Change in daily doses of patient-reported inhaled corticosteroids (ICS) intake from baseline to week 12, 24 and 52 after first benralizumab dose; Reduction (in percentage) in prescribed daily ICS dose intake from baseline to week 52 a...

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov