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Comparison · NCT01326546-cf332143

Therapeutic HBV Vaccine+Entecavir vs Placebo+Entecavir: Percentage of Participants With HBeAg Seroconversion at Week 48

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. Therapeutic HBV Vaccine+Entecavir vs Placebo+Entecavir: Percentage of Participants With HBeAg Seroconversion at Week 48. Trial comparisons, record NCT01326546-cf332143. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01326546-cf332143

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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 10.1110.07380.164wilson
Risk in group 20.1220.08290.177wilson
Risk difference, group 1 minus group 2-0.0112-0.07730.0546newcombe hybrid score
Risk ratio, group 1 over group 20.9080.5211.58log
Odds ratio, group 1 over group 20.8970.4781.68log
Number needed to treat, for one fewer participant with the outcome on Therapeutic HBV Vaccine+Entecavir than on Placebo+Entecavir89.1from 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 1Therapeutic HBV Vaccine+Entecavir
Inject εPA-44 900μg at week 0, 3, 6, 9, 12, 15, 18, 21, 24, 28, 32, 36, 40, 44, 48 and Oral intake entecavir 0.5mg per day.~Therapeutic HBV vaccine: Inject εPA-44 900μg at week 0, 3, 6, 9, 12, 15, 18, 21, 24, 28, 32, 36, 40, 44, 48.~entecavir: 0.5mg,per day,oral intake.
21189OG000
Group 2Placebo+Entecavir
Placebo comparator: Inject placebo 900μg at week 0, 3, 6, 9, 12, 15, 18, 21, 24, 28, 32, 36, 40, 44, 48 and Oral intake entecavir 0.5mg per day.~entecavir: 0.5mg,per day,oral intake.~placebo: Inject placebo 900μg at week 0, 3, 6, 9, 12, 15, 18, 21, 24, 28, 32, 36, 40, 44, 48.
23188OG001

Outcome

Type
PRIMARY
Title
Percentage of Participants With HBeAg Seroconversion at Week 48
Description
Primary endpoint data were summarised under End of Study,using the last available post-baseline observation(Last Observation Carried Forward,LOCF)
Time frame
48 weeks
Population
Intention-To-Treat Population

Source ClinicalTrials.gov

Trial

Title
Therapeutic Hepatitis B Vaccine (Mimogen-based) Joint Entecavir in Treating Chronic Hepatitis B Patients
NCT number
NCT01326546
Phases
PHASE2
Conditions
Chronic Hepatitis B
Interventions
Therapeutic HBV vaccine, entecavir, placebo
Lead sponsor
Chongqing Jiachen Biotechnology Ltd.
Results first posted
2019-06-26

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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