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Trial · NCT02498652

Results by group95

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

OutcomeGroupCategoryValueSpreadUnits
Cohort 1 - Renal Hypoxanthine Excretion at 0-24hr of Multiple-dose RDEA3170 Administered in Combination With Allopurinol (AeHXO, CB (%))Treatment A2b827Standard Error 136Percentage (%) Change
Cohort 1 - Renal Hypoxanthine Excretion at 0-24hr of Multiple-dose RDEA3170 Administered in Combination With Allopurinol (AeHXO, CB (%))Treatment R1310Standard Error 55.5Percentage (%) Change
Cohort 1 - Renal Hypoxanthine Excretion at 0-24hr of Multiple-dose RDEA3170 Administered in Combination With Allopurinol (AeHXO, CB (%))Treatment R3311Standard Error 51.8Percentage (%) Change
Cohort 1 - Renal Hypoxanthine Excretion at 0-24hr of Multiple-dose RDEA3170 Administered in Combination With Allopurinol (AeHXO, CB (%))Treatment R5305Standard Error 54.7Percentage (%) Change
Cohort 2 - Maximum Percentage (%) Change in Serum Urate of Multiple-dose RDEA3170 Administered in Combination With Allopurinol (Emax, CB (%))Treatment A1-39.3Standard Error 1.78Maximum Percentage (%) Change
Cohort 2 - Maximum Percentage (%) Change in Serum Urate of Multiple-dose RDEA3170 Administered in Combination With Allopurinol (Emax, CB (%))Treatment A2q-54.4Standard Error 4.50Maximum Percentage (%) Change
Cohort 2 - Maximum Percentage (%) Change in Serum Urate of Multiple-dose RDEA3170 Administered in Combination With Allopurinol (Emax, CB (%))Treatment A2b-50.3Standard Error 4.15Maximum Percentage (%) Change
Cohort 2 - Maximum Percentage (%) Change in Serum Urate of Multiple-dose RDEA3170 Administered in Combination With Allopurinol (Emax, CB (%))Treatment R2-57.8Standard Error 1.61Maximum Percentage (%) Change
Cohort 2 - Maximum Percentage (%) Change in Serum Urate of Multiple-dose RDEA3170 Administered in Combination With Allopurinol (Emax, CB (%))Treatment R4-66.0Standard Error 1.86Maximum Percentage (%) Change
Cohort 2 - Maximum Percentage (%) Change in Serum Urate of Multiple-dose RDEA3170 Administered in Combination With Allopurinol (Emax, CB (%))Treatment R6-73.2Standard Error 1.75Maximum Percentage (%) Change
Maximum Observed Concentration (Cmax)Treatment A11.1895% Confidence Interval 1.03 to 1.36µg/mL
Maximum Observed Concentration (Cmax)Treatment A2q2.4395% Confidence Interval 1.94 to 3.04µg/mL
Maximum Observed Concentration (Cmax)Treatment A2b1.1995% Confidence Interval 0.997 to 1.42µg/mL
Maximum Observed Concentration (Cmax)Treatment R11.1695% Confidence Interval 0.911 to 1.47µg/mL
Maximum Observed Concentration (Cmax)Treatment R21.1695% Confidence Interval 0.937 to 1.43µg/mL
Maximum Observed Concentration (Cmax)Treatment R31.1495% Confidence Interval 0.905 to 1.44µg/mL
Maximum Observed Concentration (Cmax)Treatment R41.1195% Confidence Interval 0.928 to 1.33µg/mL
Maximum Observed Concentration (Cmax)Treatment R51.1295% Confidence Interval 0.877 to 1.44µg/mL
Maximum Observed Concentration (Cmax)Treatment R61.2695% Confidence Interval 1.02 to 1.56µg/mL
Time of Occurrence of Maximum Observed Concentration (Tmax)Treatment A11.5095% Confidence Interval 0.500 to 6.02hr

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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