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Trial · NCT02888106

Outcomes13

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYPercentage of Patients With Negative HDV RNA by PCR72 weeksFASPercentage of participantsNUMBER
SECONDARYPercentage of Patients With Negative HDV RNA by PCR24 and 48 weeksFASPercentage of participantsNUMBER
SECONDARYPercentage of Patients With Normalized ALT24, 48 and 72 weeksFASPercentage of participantsNUMBER
SECONDARYPercentage of Patients With Combined Response24, 48 and 72 weeksFASPercentage of participantsNUMBER
SECONDARYPercentage of Patients With HВsAg Response24, 48 and 72 weeksFASPercentage of participantsNUMBER
SECONDARYPercentage of Patients With HBsAg Negativation48 and 72 weeksAccording to SAP Section 7.1.5 - Handling of missing data.Percentage of participantsNUMBER
SECONDARYPercentage of Patients With Negative HBV DNA by PCR24, 48 and 72 weeksPercentage of participantsNUMBER
SECONDARYThe Intensity of Liver Fibrosis Based on Results of Transient Elastometry of Liver at Weeks 48 and 72.48 and 72 weeksFASkPaMEAN
SECONDARYNumber of Participants With Change (Improvement / Worsening) in Fibrosis and Histological Activity Stage From Baseline to Post-treatment72 weeksFASParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYChange in Molecular Analyses of Relative HDV RNA Expression, Relative HBV Pregenomic Expression, Relative Total HBV RNA Expression (X Region), Relative HBV RNA Expression (S Region).48 and 72 weeksFASRelative valueMEAN
SECONDARYChange in Molecular Analyses of Total HBV DNA (X Region) Copies/Cell, HBV DNA (S Region) Copies/Cell, cccDNA Copies/Cell From Baseline to Post-treatment.48 and 72 weeksFASCopies/cellMEAN
SECONDARYChange in Molecular Analysis of HDAg Positive Hepatocytes (%) From Baseline to Post-treatment48 and 72 weeksFASPercentageMEAN
SECONDARYChange in the Gene Expression Analyses From Baseline to Post-treatmentWeeks 48 - 72FASRelative valueMEAN

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT02888106/outcomes