Trial · NCT04191304
Registered outcomes13
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 13 of 13
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Time to First HES Worsening/Flare During the DB Treatment Period | DB period (Baseline to Week 24) | The time to first HES worsening/flare is calculated as: start date of the first HES worsening - date of randomisation + 1. For participants who do not experience a HES worsening/flare, the time to first HES worsening/flare is right censored at the end of the DB period corresponding to the earliest date (date of the first of Benra open label dose, study day 183, date of last contact, and data cut-off date). The number of participants with events and censored observations is presented. |
| Secondary | Proportion of Patients Who Experience an HES Worsening/Flare During the DB Treatment Period | DB period (Baseline to Week 24) | The proportion of participants who experience an HES worsening/flare or who withdraw from the study prior to completing the 24-week DB treatment period. The proportion is calculated as the number of participants with an HES worsening/flare or withdrawal divided by the total number of participants in the analysis population. The number and proportion (expressed as percentage) or participants who experienced HES worsening/flare is presented. |
| Secondary | Number of HES Worsenings/Flares (Annualised Rate) During the DB Period | DB period (Baseline to Week 24) | The annualised rate of HES worsening/flare events was analysed using a negative binomial regression model adjusted for region, with the logarithm of follow-up time included as an offset variable. Annualized flare rates are model estimated marginal rates. A separate HES worsening/flare is considered if the start date of an HES worsening/flare is at least 14 days apart from the stop date of a preceding HES worsening/flare. |
| Secondary | Time to First Haematologic Relapse (AEC ≥ 1000 Cells/μL) During the DB Period | DB period (Baseline to Week 24) | Time to first haematologic relapse is calculated as start date of the first haematologic relapse - date of randomisation + 1. Haematologic relapse is defined as the first occurrence of an absolute eosinophil count (AEC) ≥ 1000 cells/μL post-baseline. For participants who do not experience haematologic relapse, the time to first haematologic relapse is right censored at the end of the DB period corresponding to the earliest date of (date of the first of Benra open label dose, study day 183, date of last contact, and data cut-off date). The number of participants with events and censored observations is presented. |
| Secondary | Fatigue Severity (PROMIS Fatigue Short Form 7a) at Week 24 | Week 24 | Fatigue severity was assessed using the Patient-Reported Outcomes Measurement Information System (PROMIS) Fatigue Short Form 7a questionnaire. Each item is scored on a 5-point Likert scale (1 to 5), and the total raw score is converted to a T-score. T-scores are standardized such that 50 represents the population mean with a standard deviation of 10. Standardized T-score range is from 29.4 to 83.2, with higher scores indicating more severe fatigue. A reduction in T-score indicates an improvement in fatigue severity. The least squares (LS) mean (95% CI) change from baseline in T-score at Week 24 is presented. |
| Secondary | Proportion of Patients Who Have Haematologic Relapse During the DB Treatment Period | DB period (Baseline to Week 24) | The proportion of patients who have a haematologic relapse or withdraw from the study over the DB treatment period is defined as the number of participants who have a first haematologic relapse or withdraw prior to completing in the DB period divided by the number of participants in the the analysis. Haematologic relapse is defined when AEC post baseline is ≥ 1,000 cells/Ul for the first time. The number and proportion (expressed as percentage) of participants who experienced haematologic relapse is presented. |
| Secondary | Proportion of Patients Who Have AEC < 500 Cells/μL for 24 Weeks | DB period (Baseline to Week 24) | The proportion of participants who maintained an AEC of \< 500 cells/µL throughout the 24-week DB treatment period. The proportion is defined as the number of participants who maintained AEC \< 500 cells/µL divided by the total number of participants in the analysis population. The number and proportion (expressed as percentage) of participants who maintained AEC \< 500 cells/µL is presented. |
| Secondary | Proportion of Patients Who Require an Increase in Corticosteroid Dose From Baseline at Any Point in the DB Treatment Period | DB period (Baseline to Week 24) | The proportion of patients who required an increase in systemic corticosteroids (SCS) from baseline during the 24-week DB treatment period. An increase in SCS includes an increase of at least 1 mg prednisone equivalent for participants receiving oral corticosteroids at baseline, or initiation of a new or additional course of systemic corticosteroids for treatment of HES or a closely related condition. Baseline is defined as the last valid value on or prior to randomisation. The number and proportion (expressed as percentage) of participants who require an increase in SCS from baseline. |
| Secondary | Health-Related Quality of Life (HRQoL) (Short Form-36 Version 2 [SF-36v2]) | DB period (Baseline to Week 24) | HRQoL was assessed using the 36 Item Short Form Health Survey, version 2 (SF 36v2). Change from baseline in HRQoL was evaluated using the Physical Component Summary (PCS) and Mental Component Summary (MCS) scores at Week 12 and Week 24 during the DB treatment period. PCS and MCS scores are norm-based and standardized to a general population with a mean of 50 and a standard deviation of 10, with higher scores indicating better HRQoL. Scores generally range from 0 to 100. PCS and MCS scores are derived from weighted combinations of domain scores using standard scoring algorithms. An increase in score indicates an improvement. LS mean (95% CI) changes from baseline for PCS and MCS scores are presented. |
| Secondary | Patient Global Impression of Severity (PGI-S) | DB period (Baseline to Week 24) | Patient Global Impression of Severity (PGI-S) is a single-item, participant-reported assessment of disease severity during the DB treatment period. PGI-S captures the participant's perception of overall symptom severity at the time of assessment using categorical response options ranging from "No symptoms" to "Very severe". The number and percentage of participants in each response category are presented at each timepoint. |
| Secondary | Patient Global Impression of Change (PGI-C) | DB period (Baseline to Week 24) | Patient Global Impression of Change (PGI-C) is a single-item, participant-reported assessment that captures the participant's overall evaluation of response to treatment during the DB treatment period. PGI-C reflects the participant's perception of change in disease status compared with baseline using categorical response options ranging from "Much better" to "Much worse." The number and percentage of participants in each response category are presented at each time point. |
| Secondary | Serum Benralizumab Concentrations | DB period (Baseline to Week 24) | Serum concentrations of benralizumab measured over time during the DB period to characterise the pharmacokinetics of benralizumab in participants with HES. Baseline is defined as the last valid value on or prior to the date of randomisation. |
| Secondary | Anti-Benralizumab Antibodies and Neutralizing Antibodies (nAbs) | DB period (Baseline to Week 24) | Immunogenicity of benralizumab, as assessed by the incidence and prevalence of anti-drug antibodies (ADA), including nAbs, measured from baseline through the 24-week DB treatment period in participants with HES. |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
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
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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