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Trial · NCT05239221

Registered outcomes15

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

ListOutcomeTime frameDescription
PrimaryTreatment Emergent Adverse Events (TEAEs)Up to 2 weeks in Part A and Part B, and up to 3 months in Part CNumber of Treatment Emergent Adverse Events (TEAEs), as assessed by medDRA (v25).
SecondaryObserved Maximum Concentration (Cmax) - Part A24 hoursObserved maximum concentration (Cmax) of AZP-3601 (pg/mL) in Part A
SecondaryObserved Maximum Concentration (Cmax) - Part BDay 1, Day 14Observed maximum concentration (Cmax) of AZP-3601 (pg/mL) in Part B
SecondaryObserved Maximum Concentration (Cmax) - Part CDay 1, Day 14, Day 28, Day 84Observed maximum concentration (Cmax) of AZP-3601 (pg/mL) in Part C.
SecondaryArea Under the Plasma-drug Concentration Time Curve (AUC) - Part A24 hoursArea under the plasma-drug concentration time curve (AUC) (pg\*h/mL) in Part A
SecondaryArea Under the Plasma-drug Concentration Time Curve (AUC) - Part BDay 1, Day 14Area Under the Plasma-drug Concentration Time Curve (AUC) (pg\*h/mL) in Part B
SecondaryArea Under the Plasma-drug Concentration Time Curve (AUC) - Part CDay 1, Day 14, Day 28, Day 84Area Under the Plasma-drug Concentration Time Curve (AUC) (pg\*h/mL) in Part C.
SecondaryCalcium Corrected for Albumin - Part A24 hoursLevels of calcium corrected for albumin (mg/dL) in Part A
SecondaryCalcium Corrected for Albumin - Part B24 hours, Day 14Levels of calcium corrected for albumin (mg/dL) in Part B
SecondaryCalcium Corrected for Albumin - Part CDay 1, Day 14, Day 28 and Day 84Levels of calcium corrected for albumin (mg/dL) in Part C.
SecondarySerum Phosphate - Part A24 hoursSerum phosphate levels (mg/dL) in Part A
SecondarySerum Phosphate - Part BDay 1, Day 14Serum phosphate levels (mg/dL) in Part B
SecondarySerum Phosphate - Part CDay 1 (H0), Day 14 (H2), Day 28 (H2) and Day 84 (H2)Serum phosphate levels (mg/dL) in Part C.
SecondaryDaily Dose of Oral Calcium and Active Vitamin D - Part CDay 28 and Day 43Daily dose of oral calcium and active vitamin D for patients treated in Part C.
OtherCalcium Excretion Rate 24h- Part CDay 1, Day 14, Day 28 and Day 8424 hour calcium excretion rate (mg/24h) in Part C.

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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