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Trial · NCT03205150

Outcomes11

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange From Baseline in Alanine Aminotransferase (ALT) at Week 12Baseline, Week 12Pharmacodynamics (PD) analysis set: included all participants with available PD data, who received any study drug and had valid measurements for the outcome measureUnits per Liter (U/L)MEAN
SECONDARYChange From Baseline in Percent Liver Fat at Week 12Baseline, Week 12Pharmacodynamics (PD) analysis set: included all participants with available PD data, who received any study drug and had valid measurements for the outcome measurePercentage of Liver FatMEAN
SECONDARYPercent Change From Baseline in Total Body Weight at Week 12Baseline, Week 12Pharmacodynamics (PD) analysis set: included all participants with available PD data, who received any study drug and had valid measurements for the outcome measurepercentage changeMEAN
SECONDARYChange From Baseline in Non-invasive Markers of Hepatic Fibrosis: Enhanced Liver Fibrosis Test (ELF) Score at Week 12Baseline, Week 12Pharmacodynamics (PD) analysis set: included all participants with available PD data, who received any study drug and had valid measurements for the outcome measurescores on a scaleMEAN
SECONDARYChange From Baseline in the Concentration of Hyaluronic Acid at Week 12.Baseline, Week 12Pharmacodynamics (PD) analysis set: included all participants with available PD data, who received any study drug and had valid measurements for the outcome measureug/LMEAN
SECONDARYChange From Baseline in the Concentration of Procollagen Type Iii N-Terminal Peptide (PIIINP) at Week 12.Baseline, Week 12Pharmacodynamics (PD) analysis set: included all participants with available PD data, who received any study drug and had valid measurements for the outcome measureug/LMEAN
SECONDARYChange From Baseline in the Concentration of Tissue Inhibitor Of Metalloproteinase 1 (TIMP-1) at Week 12.Baseline, Week 12Pharmacodynamics (PD) analysis set: included all participants with available PD data, who received any study drug and had valid measurements for the outcome measureug/LMEAN
SECONDARYPharmacokinetics of LIK066: Observed Maximum Plasma Concentration (Cmax) Following Drug AdministrationDay 56 (pre-dose and 1, 2, 4 and 6 hours post-dose)Pharmacokinetics (PK) analysis set consisted of LIK066 treated patients. Placebo patients were excluded from the PK analysisng/mLMEAN
SECONDARYPharmacokinetics of LIK066: Observed Maximum Time Duration of Maximum Concentration (Tmax) Following Drug AdministrationDay 56 (pre-dose and 1, 2, 4 and 6 hours post-dose)Pharmacokinetics (PK) analysis set consisted of LIK066 treated patients. Placebo patients were excluded from the PK analysishoursMEDIAN
SECONDARYPharmacokinetics of LIK066: Observed Area Under the Curve up to the Last Measurable Concentration (AUClast) Following Drug AdministrationDay 56 (pre-dose and 1, 2, 4 and 6 hours post-dose)Pharmacokinetics (PK) analysis set consisted of LIK066 treated patients. Placebo patients were excluded from the PK analysishour*ng/mLMEAN
SECONDARYChange From Baseline in Aspartate Aminotransferase (AST) at Week 12Baseline, Week 12Pharmacodynamics (PD) analysis set: included all participants with available PD data, who received any study drug and had valid measurements for the outcome measureUnits per liter (U/L)MEAN

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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GET https://conductscience.org/api/trials/v1/NCT03205150/outcomes