ConductScience.org, home

Comparison · NCT04343976-1e1e3753

Lambda Treatment vs Saline Placebo: Undetectable COVID PCR Testing at Day 14

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

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

Download JSON
Cite this record

ConductScience Library. Lambda Treatment vs Saline Placebo: Undetectable COVID PCR Testing at Day 14. Trial comparisons, record NCT04343976-1e1e3753. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04343976-1e1e3753

On this page

Measures6

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

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.3330.09680.7wilson
Risk in group 20.3330.09680.7wilson
Risk difference, group 1 minus group 20-0.4360.436newcombe hybrid score
Risk ratio, group 1 over group 210.2024.95log
Odds ratio, group 1 over group 210.090711log
Number needed to treatfrom the risk difference intervalthe two groups' risks are equal

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 lambda26OG000
Group 2Saline PlaceboSubcutaneous injection of saline placebo~Pegylated interferon lambda: 180 mcg subcutaneous injection of pegylated interferon lambda26OG001

Outcome

Type
SECONDARY
Title
Undetectable COVID PCR Testing at Day 14
Description
Negative COVID PCR testing 14 days after first lambda dose
Time frame
14 days
Population
All subjects providing NP swab samples at Day 14

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.

For software

Read this comparison from software.

The record is JSON. No key.

GET https://conductscience.org/api/comparisons/v1/NCT04343976-1e1e3753