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Trial · NCT04480840

Results by group38

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With Treatment Emergent Adverse EventsPlacebo21Participants
Number of Participants With Treatment Emergent Adverse EventsPLN-74809 Dose Level 110Participants
Number of Participants With Treatment Emergent Adverse EventsPLN-74809 Dose Level 216Participants
Number of Participants With Treatment Emergent Adverse EventsPLN-74809 Dose Level 315Participants
Number of Participants With Treatment Emergent Adverse EventsPLN-74809 Dose Level 423Participants
Number of Participants With Serious Treatment Emergent Adverse EventsPlacebo1Participants
Number of Participants With Serious Treatment Emergent Adverse EventsPLN-74809 Dose Level 11Participants
Number of Participants With Serious Treatment Emergent Adverse EventsPLN-74809 Dose Level 21Participants
Number of Participants With Serious Treatment Emergent Adverse EventsPLN-74809 Dose Level 30Participants
Number of Participants With Serious Treatment Emergent Adverse EventsPLN-74809 Dose Level 41Participants
Assessment of PLN-74809 Total Plasma Concentrations at Week 12PLN-74809 Placebo0.00Standard Deviation 0.00ng/mL
Assessment of PLN-74809 Total Plasma Concentrations at Week 12PLN-74809 Dose Level 1638.71Standard Deviation 378.193ng/mL
Assessment of PLN-74809 Total Plasma Concentrations at Week 12PLN-74809 Dose Level 2843.06Standard Deviation 474.312ng/mL
Assessment of PLN-74809 Total Plasma Concentrations at Week 12PLN-74809 Dose Level 32035.95Standard Deviation 1020.567ng/mL
Assessment of PLN-74809 Total Plasma Concentrations at Week 12PLN-74809 Dose Level 43667.50Standard Deviation 1598.067ng/mL
Assessment of PLN-74809 Total Plasma Concentrations at Week 24PLN-74809 Placebo0.00Standard Deviation 0.00ng/mL
Assessment of PLN-74809 Total Plasma Concentrations at Week 24PLN-74809 Dose Level 43583.64Standard Deviation 1642.404ng/mL
Assess Change From Baseline in Enhanced Liver Fibrosis (ELF) at Week 12Placebo0.42Standard Deviation 0.75Unitless
Assess Change From Baseline in Enhanced Liver Fibrosis (ELF) at Week 12PLN-74809 Dose Level 10.16Standard Deviation 0.58Unitless
Assess Change From Baseline in Enhanced Liver Fibrosis (ELF) at Week 12PLN-74809 Dose Level 20.19Standard Deviation 0.51Unitless

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.

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