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Trial · NCT03296800

Results by group66

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

OutcomeGroupCategoryValueSpreadUnits
Cmax (Maximum Observed Plasma Concentration)Study 1: Bexagliflozin Alone161.675Geometric Coefficient of Variation 28.673ng/mL
Cmax (Maximum Observed Plasma Concentration)Study 1: Bexagliflozin and Probenecid193.366Geometric Coefficient of Variation 22.098ng/mL
Cmax (Maximum Observed Plasma Concentration)Study 2: Bexagliflozin Alone97.811Geometric Coefficient of Variation 53.903ng/mL
Cmax (Maximum Observed Plasma Concentration)Study 2: Bexagliflozin and Rifampin117.001Geometric Coefficient of Variation 60.097ng/mL
Cmax (Maximum Observed Plasma Concentration)Study 3: Bexagliflozin Alone159.355Geometric Coefficient of Variation 35.396ng/mL
Cmax (Maximum Observed Plasma Concentration)Study 3: Bexagliflozin and Verapamil169.000Geometric Coefficient of Variation 24.727ng/mL
Tmax (Time of Maximum Observed Plasma Concentration)Bexagliflozin/ProbenecidBexagliflozin alone2.000Full Range 2.000 to 4.000hours
Tmax (Time of Maximum Observed Plasma Concentration)Bexagliflozin/RifampinBexagliflozin alone2.000Full Range 2.000 to 4.083hours
Tmax (Time of Maximum Observed Plasma Concentration)Bexagliflozin/VerapamilBexagliflozin alone3.0Full Range 2.000 to 8.000hours
Tmax (Time of Maximum Observed Plasma Concentration)Bexagliflozin/ProbenecidBexagliflozin + additional drug3.000Full Range 2.000 to 4.017hours
Tmax (Time of Maximum Observed Plasma Concentration)Bexagliflozin/RifampinBexagliflozin + additional drug2.000Full Range 1.017 to 4.000hours
Tmax (Time of Maximum Observed Plasma Concentration)Bexagliflozin/VerapamilBexagliflozin + additional drug3.000Full Range 2.000 to 4.000hours
T1/2 (Apparent Terminal Elimination Half-life)Bexagliflozin/ProbenecidBexagliflozin alone12.090Geometric Coefficient of Variation 35.950hours
T1/2 (Apparent Terminal Elimination Half-life)Bexagliflozin/RifampinBexagliflozin alone12.190Geometric Coefficient of Variation 36.966hours
T1/2 (Apparent Terminal Elimination Half-life)Bexagliflozin/VerapamilBexagliflozin alone10.709Geometric Coefficient of Variation 44.103hours
T1/2 (Apparent Terminal Elimination Half-life)Bexagliflozin/ProbenecidBexagliflozin + additional drug13.894Geometric Coefficient of Variation 24.806hours
T1/2 (Apparent Terminal Elimination Half-life)Bexagliflozin/RifampinBexagliflozin + additional drug5.318Geometric Coefficient of Variation 49.740hours
T1/2 (Apparent Terminal Elimination Half-life)Bexagliflozin/VerapamilBexagliflozin + additional drug11.675Geometric Coefficient of Variation 48.222hours
AUC0-inf (Area Under the Plasma Concentration-time Curve From Time 0 to Infinity)Study 1: Bexagliflozin Alone1118.741Geometric Coefficient of Variation 23.290hr*ng/mL
AUC0-inf (Area Under the Plasma Concentration-time Curve From Time 0 to Infinity)Study 1: Bexagliflozin/Probenecid1583.188Geometric Coefficient of Variation 23.676hr*ng/mL

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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