Phase 2 Asthma Trial, Recruiting NCT07282886 Sponsor: University of Alabama at Birmingham Condition: Asthma
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Phase 2 Asthma Trial, Recruiting

NCT07282886
Recruiting Phase 2

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:

  • People aged 18 to 75 years old
  • People with a confirmed asthma diagnosis, with a documented history of asthma for at least 1 year, where the diagnosis was made before age 40, and/or whose lung function test results fall within a specific range (confirm with trial site)
  • People whose asthma symptoms are not well controlled despite using a combination inhaler (containing both a steroid and a long-acting reliever), as measured by a standard asthma control score below 20
  • People who have not had a severe asthma episode in the past 3 months that required steroid tablets, an emergency department visit, or a hospital stay
  • People who are able to learn and correctly use two types of inhalers (a pressurised metered dose inhaler and a dry powder inhaler)
  • People who are willing and able to follow study procedures, including lung function tests performed sitting and lying down, and who understand the risks involved
  • Women who could potentially become pregnant and who are willing to use a highly effective form of contraception from the time of signing the consent form until the follow-up visit, or whose partner has been confirmed by a doctor to be unable to father children (in which case contraception is not required)
  • Women who cannot become pregnant, defined as those who have gone through menopause (no periods for 12 or more consecutive months without another medical cause) or who have had a permanent sterilisation procedure such as removal of the uterus, fallopian tubes, or ovaries
  • People who give written consent before any study-related procedures take place

Who may not be able to join:

  • People who are pregnant or breastfeeding
  • People who had a significant worsening of asthma symptoms in the 3 months before the first study visit that required steroid tablets, antibiotics, or hospitalisation
  • People who are unable to complete lung function tests or follow the study procedures and treatment requirements
  • People with a history of a life-threatening asthma attack or a past stay in an intensive care unit for asthma, where the trial doctor judges this may place the person at undue risk
  • People who have used steroid tablets, injections, or slow-release steroid medications within a certain period before screening (4 weeks for regular steroids, 12 weeks for slow-release forms)
  • People who have been diagnosed with a chronic lung disease known as COPD
  • People with a history of cystic fibrosis, bronchiectasis, alpha-1 antitrypsin deficiency, or any other significant lung condition that could interfere with study results
  • People who currently smoke or use e-cigarettes, or who have a significant smoking history (10 or more pack-years), or who stopped smoking within one year before the screening visit
  • People with a clinically significant heart condition, including moderate-to-severe heart failure, a recent heart attack (within the past year), certain heart rhythm problems diagnosed in the last 6 months, significant electrical conduction problems in the heart, or a type of irregular heartbeat called atrial fibrillation (confirm specific details with trial site)
  • People who are unable to undergo CT or MRI scans, or who have a known intolerance to Xenon gas
  • People who have taken part in another clinical treatment trial within the past 6 months
  • People who have an allergy to milk protein

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 22 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 205-975-5294

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
Phase 2
Registry
ClinicalTrials.gov
Start date
15 March 2026
Est. completion
31 December 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Evaluate the effect of extrafine beclomethasone dipropionate/formoterol fumarate /glycopyrrolate compared with non-extrafine fluticasone furoate/ umeclidinium/vilanterol on ventilation defect percentage utilizing 129Xenon MRI.

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: 22 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