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Comparison · NCT04343976-3997a46b

Lambda Treatment vs Saline Placebo: Undetectable COVID PCR at Day 7

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 7. Trial comparisons, record NCT04343976-3997a46b. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04343976-3997a46b

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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 20.5710.250.842wilson
Risk difference, group 1 minus group 2-0.429-0.7230.0615newcombe hybrid score
Risk ratio, group 1 over group 20.250.03651.71log
Odds ratio, group 1 over group 20.1250.009351.67log
Number needed to treat, for one fewer participant with the outcome on Lambda Treatment than on Saline Placebo2.33from the risk difference intervalthe interval includes no difference

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 lambda47OG001

Outcome

Type
PRIMARY
Title
Undetectable COVID PCR at Day 7
Description
Negative COVID PCR testing 7 days after first lambda dose
Time frame
7 days
Population
Subjects with Day 7 qPCR result of NEG (negative), meaning that no amplification was observed.

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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