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Trial · NCT07882732

Registered outcomes23

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryIncidence of hospitalizationDay 0 through Day +14Number and percentage of participants hospitalized.
PrimaryTime to hospital admissionDay 0 through Day +14Number of days between infusion and hospital admission, reported as median (IQR) and range.
PrimaryReason for hospitalizationDay 0 through Day +14Number and percent of participants for each hospitalization reason.
PrimaryHospital length of stayDay 0 through Day +14Number of days in hospital (midnight to midnight), reported as median (IQR) and range.
PrimaryIncidence of ICU admissionDay 0 through Day +14Number and percentage of participants admitted to an intensive care unit
PrimaryTime to ICU admissionDay 0 through Day +14Number of days between infusion and ICU admission, reported as median (IQR) and range.
PrimaryReason for ICU admissionDay 0 through Day +14Number and percent of participants for each icu admission reason.
PrimaryICU length of stayDay 0 through Day +14Number of days in ICU (midnight to midnight), reported as median (IQR) and range.
PrimaryIncidence of emergency department visitsDay 0 through Day +14Number and percentage of participants with at least one emergency department visit
PrimaryTime to first emergency department visitDay 0 through Day +14Number of days between infusion and first visit, reported as median (IQR) and range.
PrimaryReason for emergency department visitDay 0 through Day +14Number and percent of emergency department visits for each reason.
PrimaryMortalityDay 0 through Day 14Number and percentage of participants who died.
PrimaryIncidence of Cytokine Release Syndrome (CRS)Day 0 through Day +14Number and percentage of participants with CRS
PrimaryGrade of Cytokine Release Syndrome (CRS)Day 0 through Day +14Distribution of maximum CRS grade (Grade 0-4) per ASTCT consensus criteria (Lee 2019).
PrimaryTime to onset of Cytokine Release Syndrome (CRS)Day 0 through Day +14Days from infusion to CRS onset, reported as median (IQR) and range.
PrimaryIncidence of Immune Effector Cell-Associated Neurotoxicity Syndrome (ICANS)Day 0 through Day +14Number and percentage of participants with ICANS
PrimaryGrade of Immune Effector Cell-Associated Neurotoxicity Syndrome (ICANS)Day 0 through Day +14Distribution of maximum ICANS grade (Grade 0-4) per ASTCT criteria (Lee 2019).
PrimaryTime to onset of Immune Effector Cell-Associated Neurotoxicity Syndrome (ICANS)Day 0 through Day +14Days from infusion to ICANS onset, reported as median (IQR) and range.
PrimaryProphylaxis for CAR T-Related ToxicitiesDay -3 through Day +14Number and percentage of participants receiving prophylaxis (corticosteroids, anakinra, tocilizumab, other) for CAR T-related side effects, overall and by type.
PrimaryTreatment of CAR T-Related ToxicitiesDay 0 through Day +14
Number and percentage of participants receiving treatment for CAR T-related side effects (antipyretics, corticosteroids, anakinra, tocilizumab, transfusion, antibiotics, antiemetics, other), overall and by type.

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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