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Trial · NCT04375397

Results by group53

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Percentage of Participants Alive and Without Respiratory Failure Through Day 28Ibrutinib 420 mg + SOC86.480% Confidence Interval 74.4 to 93.2percentage of participants
Percentage of Participants Alive and Without Respiratory Failure Through Day 28Placebo + SOC79.280% Confidence Interval 66.9 to 87.7percentage of participants
Change in the World Health Organization (WHO)-8 Ordinal Scale From Baseline at Study Day 14Ibrutinib 420 mg + SOC-4 points2Participants
Change in the World Health Organization (WHO)-8 Ordinal Scale From Baseline at Study Day 14Placebo + SOC-4 points3Participants
Change in the World Health Organization (WHO)-8 Ordinal Scale From Baseline at Study Day 14Ibrutinib 420 mg + SOC-3 points12Participants
Change in the World Health Organization (WHO)-8 Ordinal Scale From Baseline at Study Day 14Placebo + SOC-3 points9Participants
Change in the World Health Organization (WHO)-8 Ordinal Scale From Baseline at Study Day 14Ibrutinib 420 mg + SOC-2 points5Participants
Change in the World Health Organization (WHO)-8 Ordinal Scale From Baseline at Study Day 14Placebo + SOC-2 points7Participants
Change in the World Health Organization (WHO)-8 Ordinal Scale From Baseline at Study Day 14Ibrutinib 420 mg + SOC-1 point0Participants
Change in the World Health Organization (WHO)-8 Ordinal Scale From Baseline at Study Day 14Placebo + SOC-1 point2Participants
Change in the World Health Organization (WHO)-8 Ordinal Scale From Baseline at Study Day 14Ibrutinib 420 mg + SOC0 points1Participants
Change in the World Health Organization (WHO)-8 Ordinal Scale From Baseline at Study Day 14Placebo + SOC0 points1Participants
Change in the World Health Organization (WHO)-8 Ordinal Scale From Baseline at Study Day 14Ibrutinib 420 mg + SOC1 point1Participants
Change in the World Health Organization (WHO)-8 Ordinal Scale From Baseline at Study Day 14Placebo + SOC1 point1Participants
Change in the World Health Organization (WHO)-8 Ordinal Scale From Baseline at Study Day 14Ibrutinib 420 mg + SOC3 points1Participants
Change in the World Health Organization (WHO)-8 Ordinal Scale From Baseline at Study Day 14Placebo + SOC3 points1Participants
Median Reduction in Days Spent on Supplemental OxygenIbrutinib 420 mg + SOC5.0Full Range 1 to 28days
Median Reduction in Days Spent on Supplemental OxygenPlacebo + SOC6.5Full Range 1 to 21days
All-Cause Mortality at Study Days 7, 14, 21, and 28Ibrutinib 420 mg + SOCDay 7080% Confidence Interval 0.0 to 6.9percentage of participants
All-Cause Mortality at Study Days 7, 14, 21, and 28Placebo + SOCDay 7080% Confidence Interval 0.0 to 6.4percentage of participants

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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