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Trial · NCT04343976

Pegylated Interferon Lambda Treatment for COVID-19

NCT04343976, Phase 2, Terminated, Raymond Chung; results first posted 2022-07-21

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Pegylated Interferon Lambda Treatment for COVID-19. Trials, record NCT04343976. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04343976

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Trial

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

Title
Pegylated Interferon Lambda Treatment for COVID-19
NCT number
NCT04343976
Status
Terminated
Phases
Phase 2
Enrollment
14 participants, actual
Lead sponsor
Raymond Chung
Conditions
COVID-19, COVID
Interventions
Pegylated interferon lambda
First posted
2020-04-14
Last updated
2022-07-21
Results first posted
2022-07-21
Limitations and caveats
Enrollment was slower than anticipated due to issues operationalizing outpatient follow-up for viremic subjects discharged from hospital prior to study completion, including lack of transportation and delays contracting with home health services to offer home visits. Also, study was terminated prior to meeting enrollment goal due to a decrease in eligible subjects and lack of funding.

Source ClinicalTrials.gov

Registered outcomes5

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

ListOutcomeTime frameDescription
PrimaryUndetectable COVID PCR at Day 77 daysNegative COVID PCR testing 7 days after first lambda dose
SecondaryUndetectable COVID PCR at Day 33 daysNegative COVID PCR testing 3 days after first lambda dose
SecondaryPercentage of Subjects on Lambda vs Placebo With Symptomatic Improvement2 weeksDaily symptom score improvement during treatment period
SecondaryPercentage of Subjects on Lambda vs Placebo With Improved Clinical Outcomes2 weeksTime to event for death, intubation, hospital discharge
SecondaryUndetectable COVID PCR Testing at Day 1414 daysNegative COVID PCR testing 14 days after first lambda dose

Outcomes5

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYUndetectable COVID PCR at Day 77 daysSubjects with Day 7 qPCR result of NEG (negative), meaning that no amplification was observed.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYUndetectable COVID PCR at Day 33 daysParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYPercentage of Subjects on Lambda vs Placebo With Symptomatic Improvement2 weeksinsufficient data, analysis not performed as there the symptom improvement score was not collected and not available for analysis.
SECONDARYPercentage of Subjects on Lambda vs Placebo With Improved Clinical Outcomes2 weeksData was not collected and therefor analysis not performed.
SECONDARYUndetectable COVID PCR Testing at Day 1414 daysAll subjects providing NP swab samples at Day 14ParticipantsCOUNT_OF_PARTICIPANTS

Results by group6

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

OutcomeGroupCategoryValueSpreadUnits
Undetectable COVID PCR at Day 7Lambda Treatment1Participants
Undetectable COVID PCR at Day 7Saline Placebo4Participants
Undetectable COVID PCR at Day 3Lambda Treatment1Participants
Undetectable COVID PCR at Day 3Saline Placebo4Participants
Undetectable COVID PCR Testing at Day 14Lambda Treatment2Participants
Undetectable COVID PCR Testing at Day 14Saline Placebo2Participants

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDLambda Treatment7
Overall StudySTARTEDSaline Placebo7
Overall StudyCOMPLETEDLambda Treatment7
Overall StudyCOMPLETEDSaline Placebo6
Overall StudyNOT COMPLETEDLambda Treatment0
Overall StudyNOT COMPLETEDSaline Placebo1

Adverse events14

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherShortness of BreathRespiratory, thoracic and mediastinal disordersLambda Treatment070
otherShortness of BreathRespiratory, thoracic and mediastinal disordersSaline Placebo171
otherChest PainCardiac disordersLambda Treatment070
otherChest PainCardiac disordersSaline Placebo171
otherStomach Pain (unspecified)Gastrointestinal disordersLambda Treatment171
otherStomach Pain (unspecified)Gastrointestinal disordersSaline Placebo070
otherTransaminitisHepatobiliary disordersLambda Treatment171
otherTransaminitisHepatobiliary disordersSaline Placebo070
otherICU DeliriumPsychiatric disordersLambda Treatment171
otherICU DeliriumPsychiatric disordersSaline Placebo070

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityLambda Treatment07
Total, all-cause mortalitySaline Placebo07
Total, other adverse eventsLambda Treatment37
Total, other adverse eventsSaline Placebo17
Total, serious adverse eventsLambda Treatment27
Total, serious adverse eventsSaline Placebo07

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
32788708DERIVED

Source PubMed

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 comparisons5

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

ComparisonSource
Lambda Treatment vs Saline Placebo: Undetectable COVID PCR Testing at Day 14Trial comparisons
Lambda Treatment vs Saline Placebo: Undetectable COVID PCR at Day 7Trial comparisons
Lambda Treatment vs Saline Placebo: Undetectable COVID PCR at Day 3Trial comparisons
Lambda Treatment vs Saline Placebo: deaths from any causeTrial comparisons
Lambda Treatment vs Saline Placebo: serious adverse eventsTrial comparisons

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/NCT04343976

GET https://conductscience.org/api/trials/v1/NCT04343976/registered