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Comparison · NCT05288504-038e1166

AVTX-002 vs Placebo: The Ability of AVTX-002 to Improve Asthma Control in Subjects With Poorly Controlled Non-eosinophilic Asthma (NEA) Based on the Percentage of Patients Who Experience Asthma Related Events.

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. AVTX-002 vs Placebo: The Ability of AVTX-002 to Improve Asthma Control in Subjects With Poorly Controlled Non-eosinophilic Asthma (NEA) Based on the Percentage of Patients Who Experience Asthma Related Events. Trial comparisons, record NCT05288504-038e1166. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05288504-038e1166

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.2670.160.41wilson
Risk in group 20.3110.1950.457wilson
Risk difference, group 1 minus group 2-0.0444-0.2250.14newcombe hybrid score
Risk ratio, group 1 over group 20.8570.4471.64log
Odds ratio, group 1 over group 20.8050.3232.01log
Number needed to treat, for one fewer participant with the outcome on AVTX-002 than on Placebo22.5from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1AVTX-002AVTX-002: Dose of 600 mg administered subcutaneously three times during the study.1245OG000
Group 2PlaceboPlacebo: Placebo sourced as normal saline administered subcutaneously three times during the study.1445OG001

Outcome

Type
PRIMARY
Title
The Ability of AVTX-002 to Improve Asthma Control in Subjects With Poorly Controlled Non-eosinophilic Asthma (NEA) Based on the Percentage of Patients Who Experience Asthma Related Events.
Description
Percentage of patients who experience any of the following asthma related events:~* ≥6 additional reliever puffs of Short-Acting Beta-Agonist (compared to baseline) in a 24-hour period on 2 consecutive days or,~* increase in inhaled corticosteroid dose ≥4 times than the dose at baseline or,~* a decrease in peak flow of 30% or more (compared to baseline) on 2 consecutive days of treatment, or~* an asthma exacerbation requiring the use of systemic corticosteroids (tablets, suspension, or injection) for at least 3 days, or~* a hospitalization or emergency room visit because of an asthma exacerbation
Time frame
Through Week 14
Population
Full Analysis Set

Source ClinicalTrials.gov

Trial

Title
A Study to Evaluate the Safety and Efficacy of AVTX-002 for the Treatment of Poorly Controlled Non-Eosinophilic Asthma.
NCT number
NCT05288504
Phases
PHASE2
Conditions
Non-Eosinophilic Asthma
Interventions
AVTX-002, Placebo
Lead sponsor
Avalo Therapeutics, Inc.
Results first posted
2024-09-05

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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