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Comparison · NCT04343976-cd1f36a9

Lambda Treatment vs Saline Placebo: Undetectable COVID PCR at Day 3

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Lambda Treatment vs Saline Placebo: Undetectable COVID PCR at Day 3. Trial comparisons, record NCT04343976-cd1f36a9. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04343976-cd1f36a9

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.1430.02570.513wilson
Risk in group 20.6670.30.903wilson
Risk difference, group 1 minus group 2-0.524-0.788-0.00271newcombe hybrid score
Risk ratio, group 1 over group 20.2140.0321.43log
Odds ratio, group 1 over group 20.08330.005531.26log
Number needed to treat, for one fewer participant with the outcome on Lambda Treatment than on Saline Placebo1.911.27370from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Lambda TreatmentTreatment with subcutaneous injection (180 mcg) of pegylated interferon lambda~Pegylated interferon lambda: 180 mcg subcutaneous injection of pegylated interferon lambda17OG000
Group 2Saline PlaceboSubcutaneous injection of saline placebo~Pegylated interferon lambda: 180 mcg subcutaneous injection of pegylated interferon lambda46OG001

Outcome

Type
SECONDARY
Title
Undetectable COVID PCR at Day 3
Description
Negative COVID PCR testing 3 days after first lambda dose
Time frame
3 days
Population

Source ClinicalTrials.gov

Trial

Title
Pegylated Interferon Lambda Treatment for COVID-19
NCT number
NCT04343976
Phases
PHASE2
Conditions
COVID-19, COVID
Interventions
Pegylated interferon lambda
Lead sponsor
Raymond Chung
Results first posted
2022-07-21

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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