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Completed

NCT Number: NCT01071070

Evaluate Safety and Efficacy of Paricalcitol in Reducing Serum Intact Parathyroid Hormone in Chronic Kidney Disease

Evaluate Safety and Efficacy of Paricalcitol in Reducing Serum Intact Parathyroid Hormone in Chronic Kidney Disease

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Key information

About this study

Evaluate the safety and efficacy of paricalcitol injection with two different dosing regimens (currently approved dosing regimen used in the US package insert versus dosing based on a formula of iPTH/80 that was approved and used in the EU package insert) in Chronic Kidney Disease (CKD) Stage 5 subjects with secondary hyperparathyroidism receiving hemodialysis.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subject is a Chinese male or female greater than or equal to 20 years old.
  • Subject is diagnosed with Chronic Kidney Disease Stage 5 and must be on maintenance hemodialysis three times a week for at least 2 months prior to the Screening Visit and expected to remain on hemodialysis for the duration of the study.
  • For entry into the Treatment Phase, the subject must have:
  • Intact parathyroid hormone greater than or equal to 300 pg/mL
  • Serum calcium less than 10.2 mg/dL (2.55 mmol/L)
  • Calcium-phosphorus product less than 65 mg^2/dL^2

Exclusion criteria

  • Subject has a history of an allergic reaction or significant sensitivity to vitamin D or vitamin D related compounds.
  • Subject received a partial parathyroidectomy within one year prior to the Screening Phase.
  • Subject with New York Heart Association (NYHA) Class III or IV.
  • Subject has taken aluminum-containing phosphate binders for greater than 3 weeks in the last 3 months prior to the Screening Phase, or requires such medications for greater than 3 weeks in the study.
  • Subject has a current malignancy (with the exception of basal or squamous cell carcinoma of the skin), or clinically significant liver disease, in the opinion of the Investigator.
  • Subject has a history of drug or alcohol abuse within 6 months prior to the Screening Phase.
  • Subject is known to be human immunodeficiency virus (HIV) positive.
  • Subject has evidence of poor compliance with diet, medication or hemodialysis that may interfere, in the Investigator's opinion, with adherence to the protocol.

Treatment and study plan

Paricalcitol

Drug

Initiation dosing based on 2 approved package inserts , followed by a dose adjusted by limited chemistry test value. See Arm Description for additional details.

Other names: ABT-358, Zemplar

Primary outcomes

  1. The Achievement of Two Consecutive Greater Than or Equal to 30% Decreases From Baseline Intact Parathyroid Hormone Levels

    Time frame: Baseline to 12 Weeks

    The number of participants who achieved (Yes) or did not achieve (No) two consecutive decreases of greater than or equal to 30% from baseline in intact parathyroid hormone (iPTH) values

Secondary outcomes

  1. The Proportion of Subjects Achieving a Final Intact Parathyroid Hormone Value Between 150 and 300 pg/mL

    Time frame: Baseline to 12 Weeks

    The number of subjects with (Yes) or without (No) final intact parathyroid hormone (iPTH) values between 150 and 300 pg/mL

  2. The Change From Baseline to the Final Observation in Intact Parathyroid Hormone Value

    Time frame: Baseline to 12 Weeks

  3. The Change From Baseline to the Final Observation in Calcium

    Time frame: Baseline to 12 Weeks

  4. The Change From Baseline to the Final Observation in Calcium-phosphorus Product

    Time frame: Baseline to 12 Weeks

  5. The Change From Baseline to the Final Observation in the Vital Sign of Systolic Blood Pressure

    Time frame: Baseline to 12 Weeks

  6. The Change From Baseline to the Final Observation in the Vital Sign of Diastolic Blood Pressure

    Time frame: Baseline to 12 Weeks

  7. The Change From Baseline to the Final Observation in the Vital Sign of Heart Rate

    Time frame: Baseline to 12 Weeks

  8. The Proportion of Subjects With 2 Consecutive Calcium Measurements Greater Than 11.0 mg/dL (2.75 mmol/L)

    Time frame: Baseline to 12 weeks

    The number of subjects with (Yes) or without (No) two consecutive calcium measurements greater than 11.0 mg/dL (2.75 mmol/L)

Sponsors and collaborators

Lead sponsor

Abbott

Industry

Registry information

Official study title

A Phase 3b, Randomized, Active-Controlled, Single-Blind, Multicenter Study to Evaluate the Safety and Efficacy of Paricalcitol Injection in Reducing Serum Intact Parathyroid Hormone Levels in Chronic Kidney Disease Stage 5 Subjects Receiving Hemodialysis

Important dates

Study start
2009
Primary completion
2010
Study completion
2010
First posted
Feb 19, 2010
Registry last updated
Jan 26, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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