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Trial · NCT06853171

Registered outcomes15

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryNumber of participants with Adverse Events (AEs)Up to Day 43
PrimaryNumber of participants with Serioues AEs (SAEs)Up to Day 43
PrimaryNumber of participants with AEs of Special Interest (AESIs)Up to Day 43
SecondaryMaximum observed plasma concentration (Cmax)Up to Day 15
SecondaryArea under the concentration-time curve in 1 dosing interval (AUC(TAU))Up to Day 15
SecondaryArea under the plasma concentration-time curve from time zero to time of last quantifiable concentration (AUC(0-T))Up to Day 15
SecondaryTime of maximum observed plasma concentration (Tmax)Up to Day 15
SecondaryConcentration at the end of a dosing interval (Ctau)Up to Day 15
SecondaryCmax accumulation index (AI_Cmax)Up to Day 15Ratio of maximum observed plasma concentration at steady-state on Day 5 to maximum observed plasma concentration after first dose
SecondaryAUC accumulation index (AI_AUC)Up to Day 15Ratio of area under the concentration-time curve in 1 dosing interval at steady-state on Day 5 to area under the concentration-time curve in 1 dosing interval after first dose
SecondaryCtau accumulation index (AI_Ctau)Up to Day 15Ratio of concentration at the end of the dosing interval at steady-state on Day 5 to maximum observed plasma concentration after first dose
SecondaryAverage concentration within a dosing interval at steady-state (Css-avg)Up to Day 15
SecondaryApparent total body clearance (CLT/F)Up to Day 15
SecondaryEffective elimination half-life during dosing interval (T-HALF(eff))Up to Day 15
SecondaryT-HALFeff based on AUC observed (T-HALFeff_AUC)Up to Day 15Effective elimination half-life based on degree of area under the plasma concentration-time curve accumulation observed

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/NCT06853171/registered