ConductScience.org, home

Comparison · NCT02731131-e9463f6a

Group A: Monotherapy With Peginterferon Alfa-2a vs Group B: Combination With Peginterferon Alfa-2a + Ribavirin: Number of Participants With Negative HDV RNA at End of Treatment

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. Group A: Monotherapy With Peginterferon Alfa-2a vs Group B: Combination With Peginterferon Alfa-2a + Ribavirin: Number of Participants With Negative HDV RNA at End of Treatment. Trial comparisons, record NCT02731131-e9463f6a. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02731131-e9463f6a

On this page

Measures6

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

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.1670.03010.564wilson
Risk in group 20.3330.09680.7wilson
Risk difference, group 1 minus group 2-0.167-0.5580.295newcombe hybrid score
Risk ratio, group 1 over group 20.50.06024.15log
Odds ratio, group 1 over group 20.40.02596.18log
Number needed to treat, for one fewer participant with the outcome on Group A: Monotherapy With Peginterferon Alfa-2a than on Group B: Combination With Peginterferon Alfa-2a + Ribavirin6from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Group A: Monotherapy With Peginterferon Alfa-2aParticipants received peginterferon alfa-2a for 48 weeks as 180 mcg once weekly via SC injection.16OG000
Group 2Group B: Combination With Peginterferon Alfa-2a + Ribavirin
Participants received peginterferon alfa-2a plus ribavirin for 48 weeks. Peginterferon alfa-2a was given as 180 mcg once weekly via SC injection. Ribavirin was administered as 1000 to 1200 mg per day in divided (morning/evening) oral doses. The specific dose was determined according to the participant's body weight at Baseline.
26OG001

Outcome

Type
SECONDARY
Title
Number of Participants With Negative HDV RNA at End of Treatment
Description
Negative HDV RNA was defined as HDV RNA not detected by PCR. The number of participants with negative HDV RNA at the end of treatment (Week 48) was reported.
Time frame
Week 48
Population
ITT Population.

Source ClinicalTrials.gov

Trial

Title
A Study of Peginterferon Alfa-2a With or Without Ribavirin in Participants With Chronic Hepatitis D (CHD)
NCT number
NCT02731131
Phases
PHASE2
Conditions
Hepatitis D, Chronic
Interventions
Peginterferon alfa-2a, Ribavirin
Lead sponsor
Hoffmann-La Roche
Results first posted
2016-07-15

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/NCT02731131-e9463f6a