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Trial · NCT05636891

Registered outcomes12

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

ListOutcomeTime frameDescription
PrimaryPK parameters comparison between NNG-DEPO and Aranesp®: CmaxIV:Assessed predose and at 0.25; 0.5; 4;12;24;48;96;144;240;336 hours postdose/ SC: Assessed predose and at 4;12;24;48;96;144;240;336 hours postdoseSerum peak concentrations (Cmax)
PrimaryPK parameters comparison between NNG-DEPO and Aranesp®: AUC(0, t)IV:Assessed predose and at 0.25; 0.5; 4;12;24;48;96;144;240;336 hours postdose/ SC: Assessed predose and at 4;12;24;48;96;144;240;336 hours postdoseArea under the curve from 0 to t (AUC 0-t)
SecondaryPD parameters comparison between NNG-DEPO and Aranesp®: Cmax of reticulocytesAssessed predose and at and at 24;48;96;144;240;336 hours postdoseSerum peak concentrations (Cmax) of reticulocytes
SecondaryPD parameters comparison between NNG-DEPO and Aranesp®: AUC(0, t) of reticulocytesAssessed predose and at and at 24;48;96;144;240;336 hours postdoseArea under the curve from 0 to t (AUC 0-t) of reticulocytes
SecondaryPD parameters comparison between NNG-DEPO and Aranesp®: Tmax of reticulocytesAssessed predose and at and at 24;48;96;144;240;336 hours postdoseTime for the drug to reach peak concentration (Tmax) of reticulocytes
SecondaryPK parameters comparison between NNG-DEPO and Aranesp®:TmaxIV:Assessed predose and at 0.25; 0.5; 4;12;24;48;96;144;240;336 hours postdose/ SC: Assessed predose and at 4;12;24;48;96;144;240;336 hours postdoseTime for the drug to reach peak concentration (Tmax)
SecondaryPK parameters comparison between NNG-DEPO and Aranesp®: AUC(0,∞)IV:Assessed predose and at 0.25; 0.5; 4;12;24;48;96;144;240;336 hours postdose/ SC: Assessed predose and at 4;12;24;48;96;144;240;336 hours postdoseArea under the curve from 0 to ∞ (AUC0-∞)
SecondaryPK parameters comparison between NNG-DEPO and Aranesp®:T1/2IV:Assessed predose and at 0.25; 0.5; 4;12;24;48;96;144;240;336 hours postdose/ SC: Assessed predose and at 4;12;24;48;96;144;240;336 hours postdoseHalf-life (T1/2)
SecondaryPK parameters comparison between NNG-DEPO and Aranesp®: CL/FIV:Assessed predose and at 0.25; 0.5; 4;12;24;48;96;144;240;336 hours postdose/ SC: Assessed predose and at 4;12;24;48;96;144;240;336 hours postdoseCL/F
SecondaryPK parameters comparison between NNG-DEPO and Aranesp®:Vz/FIV:Assessed predose and at 0.25; 0.5; 4;12;24;48;96;144;240;336 hours postdose/ SC: Assessed predose and at 4;12;24;48;96;144;240;336 hours postdoseVz/F
SecondaryPK parameters comparison between NNG-DEPO and Aranesp®: λz.IV:Assessed predose and at 0.25; 0.5; 4;12;24;48;96;144;240;336 hours postdose/ SC: Assessed predose and at 4;12;24;48;96;144;240;336 hours postdoseλz.
SecondaryProportion of the adverse events (AE) including physical examinations, vital signs, and clinical laboratory investigations.Week 0 (Assessed predose)- Week 24]Rate of AE and SAE occurence

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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