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Trial · NCT04370834

Tocilizumab for Patients With Cancer and COVID-19 Disease

NCT04370834, Phase 2, Terminated, National Cancer Institute (NCI); results first posted 2021-06-04

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Tocilizumab for Patients With Cancer and COVID-19 Disease. Trials, record NCT04370834. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04370834

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Tocilizumab for Patients With Cancer and COVID-19 Disease
NCT number
NCT04370834
Status
Terminated
Phases
Phase 2
Enrollment
1 participants, actual
Lead sponsor
National Cancer Institute (NCI)
Conditions
Hematopoietic and Lymphoid Cell Neoplasm, Malignant Solid Neoplasm, Pneumonia, Pneumonitis, Severe Acute Respiratory Distress Syndrome, Symptomatic COVID-19 Infection Laboratory-Confirmed
Interventions
Tocilizumab
First posted
2020-05-01
Last updated
2025-02-04
Results first posted
2021-06-04
Limitations and caveats
Early termination as randomized data did not support continuation.

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryNumber of Participants With at Least 1 Point Reduction in Score on 7-category Clinical Status Ordinal ScaleDay 14 after tocilizumab administration
7-category Clinical Status Ordinal Scale: 1. Discharge 2. Non-ICU, hospital ward, No O2 3. Non-ICU, hospital ward, on O2 4. ICU or non-ICU, requires non-invasive ventilatory support or high flow O2 5. ICU requires mechanical or imminent ventilation/intubation 6. ICU requires ECMO and additional O2 support and organ support, e.g. vasopressors, renal replacement therapy 7. Death

Outcomes1

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYNumber of Participants With at Least 1 Point Reduction in Score on 7-category Clinical Status Ordinal ScaleDay 14 after tocilizumab administrationNo patients were accrued to Cohorts A2, B1, or B2.ParticipantsCOUNT_OF_PARTICIPANTS

Results by group1

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With at Least 1 Point Reduction in Score on 7-category Clinical Status Ordinal ScaleCohort A11Participants

Participant flow3

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDOther (Tocilizumab)1
Overall StudyCOMPLETEDOther (Tocilizumab)1
Overall StudyNOT COMPLETEDOther (Tocilizumab)0

Adverse events24

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAlanine aminotransferase increasedInvestigationsCohort A1111
otherAlanine aminotransferase increasedInvestigationsCohort A2000
otherAlanine aminotransferase increasedInvestigationsCohort B1000
otherAlanine aminotransferase increasedInvestigationsCohort B2000
otherAspartate aminotransferase increasedInvestigationsCohort A1111
otherAspartate aminotransferase increasedInvestigationsCohort A2000
otherAspartate aminotransferase increasedInvestigationsCohort B1000
otherAspartate aminotransferase increasedInvestigationsCohort B2000
otherBlood bilirubin increasedInvestigationsCohort A1111
otherBlood bilirubin increasedInvestigationsCohort A2000

Adverse event totals12

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityCohort A111
Total, all-cause mortalityCohort A200
Total, all-cause mortalityCohort B100
Total, all-cause mortalityCohort B200
Total, other adverse eventsCohort A111
Total, other adverse eventsCohort A200
Total, other adverse eventsCohort B100
Total, other adverse eventsCohort B200
Total, serious adverse eventsCohort A111
Total, serious adverse eventsCohort A200

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT04370834

GET https://conductscience.org/api/trials/v1/NCT04370834/events?page=2