Extension Study of Cinacalcet for Treatment of Secondary Hyperparathyroidism (SHPT) in Pediatric Patients With Chronic Kidney Disease on Dialysis

Amgen28 enrolled

Overview

The primary objective of this study was to characterize the long-term safety and tolerability of cinacalcet in pediatric patients with chronic kidney disease (CKD) receiving dialysis.

This extension study was designed to characterize the long-term safety and tolerability of cinacalcet in pediatric patients from Amgen Studies 20130356 (NCT02138838) and 20110100 (NCT01439867) who either had completed the parent study or were ongoing at the time an administrative decision was made to end the parent study. After enrolling into this study participants were administered cinacalcet for 28 weeks or until the time of renal transplant or parathyroidectomy, whichever occurred first. The treatment period was followed by a 4-week safety follow-up period.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Secondary Hyperparathyroidism, Chronic Kidney Disease

Interventions

CinacalcetDRUG

Cinacalcet was provided as 5 mg capsules for sprinkling or as 30 mg film-coated tablets for swallowing. The protocol-specified doses were: 1, 2.5, 5, 7.5, 10, 15, 30, 60, 90, 120, and 180 mg.

Eligibility

Sex: ALLMax age: 18 Years

Medical Language ↔ Plain English

INCLUSION CRITERIA: All subjects: * Subject's legally acceptable representative has provided informed consent when the subject is legally too young to provide informed consent and the subject has provided written assent based on local regulations and/or guidelines prior to any Study 20140159 activities/procedures being initiated. * Dialysate calcium concentration ≥ 2.5 mEq/L at day 1 All subjects with \> 14 days between the last study visit in Study 20130356 or Study 20110100 and screening for Study 20140159: * Subjects on anti-convulsant medication must be on a stable dose All subjects from 20130356: * Completed treatment through week 20 in the 20130356 study or on study at the time of Study 20130356 termination * Dry weight ≥ 12.5 kg at day 1 of Study 20140159 Subjects Randomized to the 20130356 Standard of Care Arm Only: * intact parathyroid hormone (iPTH) value ≥ 300 pg/mL (within 7 days of day 1 in Study 20140159) * Corrected calcium value ≥ 8.8 mg/dL within 7 days of day 1 in Study 20140159 All Subjects from 20110100: * Completed week 26 End of Study visit in the, 20110100 study or on study at the time of Study 20110100 termination * Dry weight ≥ 7 kg at day 1 of Study 20140159 EXCLUSION CRITERIA: General (studies 20130356 and 20110100): * Currently receiving treatment in another investigational device or drug study, or less than 30 days since ending treatment on another investigational device or drug study(s), other than Amgen Studies 20130356 or 20110100. * Other investigational procedures while participating in this study are excluded. * Malignancy except non-melanoma skin cancers, cervical or breast ductal carcinoma in situ within the last 5 years. * Subject has known sensitivity to any of the products to be administered during dosing. * Subject likely to not be available to complete all protocol-required study visits or procedures, and/or to comply with all required study procedures (eg, electronic patient diary \[ediary\]) to the best of the subject and investigator's knowledge * History or evidence of any other clinically significant disorder, condition or disease (with the exception of those outlined above) that, in the opinion of the investigator or Amgen physician, if consulted, would pose a risk to subject safety or interfere with the study evaluation, procedures, or completion. * Subject previously has entered this study. * If sexually active, subject is not willing to use acceptable contraception during treatment and for at least 9 days after the end of treatment. * Subject is pregnant or breast feeding, or planning to become pregnant during the study or within 9 days after the end of treatment * History of congenital long QT syndrome, second or third degree heart block, ventricular tachyarrythmias, or other conditions associated with prolonged QT interval * A new onset of seizures or worsening of pre-existing seizure disorder All Subjects with \> 14 days between the last study visit in Study 20130356 or Study 20110100 and the screening visit in Study 20140159 will have the following exclusion criteria applied during screening and day 1: * Unstable chronic heart failure defined as worsening pulmonary edema or other signs and symptoms as per investigator assessment during screening * Received therapy with commercial cinacalcet after the last study visit in Study 20130356 or Study 20110100 before day 1 of Study 20140159 * Scheduled date for kidney transplantation from a known living donor that makes completion of the study unlikely * Either new or recurrent cardiac ventricular arrhythmias requiring a change in treatment within 10 days prior to screening visit or day 1 of Study 20140159 screening * Hepatic impairment indicated by elevated levels of hepatic transaminase or bilirubin (aspartate aminotransferase \[AST\] ≥ 1.5 × upper limit of normal \[ULN\] OR alanine aminotransferase \[ALT\] ≥ 1.5 × ULN OR total bilirubin ≥ 1 × ULN per institutional laboratory range) during screening All Subjects - Day 1 Study Visit: * Subject has an ongoing adverse event from Studies 20130356 or 20110100 that is considered related to investigational product and is ≥ Common Terminology Criteria for Adverse Events (CTCAE) (v 4.0) grade 3, and/or considered clinically significant in the opinion of the investigator * Central laboratory values were not obtained/are not available at day 1 in Study 20140159 * Corrected QT Interval (QTc) \> 500 ms, using Bazett's formula * QTc ≥ 450 to ≤ 500 ms, using Bazett's formula, unless written permission to enroll is provided by the investigator after consultation with a pediatric cardiologist * Use of grapefruit juice, herbal medications, CYP3A4 inhibitors (eg, erythromycin, clarithromycin, ketoconazole, itraconazole), or CYP2D6 substrates (eg, flecainide, propafenone, metoprolol, desipramine, nortriptyline, clomipramine) * Use of concomitant medications that may prolong the QTc interval (eg, ondansetron, albuterol)

Locations (33)

Outcomes

Primary Outcomes

Number of Participants With Adverse Events

Adverse events (AEs) were graded according to the Common Terminology Criteria for Adverse Events (CTCAE, v4.0). The investigator assessed whether the adverse event was possibly related to the study drug as indicated by a "yes" or "no" response to the question: Is there a reasonable possibility that the event may have been caused by the study drug?

Time frame: From first dose of study drug in the extension study up to 4 weeks after the last dose; 32 weeks.

Secondary Outcomes

Percentage of Participants Achieving ≥ 30% Reduction in iPTH From Baseline to Mean Value During Weeks 11 and 15

This endpoint was analyzed in participants who received SOC only in parent study 20130356. Participants who had no iPTH values during weeks 11 or 15 were considered non-responders. Data collected more than 7 days after the last dose of study drug were excluded.

Time frame: Baseline (defined as the mean values of samples collected during the screening period and day 1 pre-dose in the extension study) and weeks 11 and 15

Percentage of Participants Achieving ≥ 30% Reduction in iPTH From Baseline to Mean Value During Weeks 23 and 28

This endpoint was analyzed in participants who received SOC only in parent study 20130356. For participants who had no values during week 23 and 28, the mean of the last 2 available post-baseline values collected in the dose-titration phase was used. If only 1 post-baseline value was available, this single value was used. If no post-baseline value was available, the participant was considered a non-responder. Data collected more than 7 days after the last dose of study drug were excluded.

Time frame: Extension study baseline and weeks 23 and 28

Percent Change From Baseline in iPTH to the Mean Value During Weeks 23 and 28

This endpoint was analyzed in participants who received SOC only in parent study 20130356. For participants who had no values during week 23 and week 28, the mean of the last 2 available post-baseline values collected in the dose-titration phase was used. If only 1 post-baseline value was available, this single value was used. If no post-baseline value was available, the participant was excluded from the analysis. Data collected more than 7 days after the last dose of study drug were excluded.

Data from ClinicalTrials.gov

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Los Angeles, California, United States

Research Site

Tucker, Georgia, United States

Research Site

Baltimore, Maryland, United States

Research Site

Boston, Massachusetts, United States

Research Site

Minneapolis, Minnesota, United States

Research Site

Jackson, Mississippi, United States

Research Site

Kansas City, Missouri, United States

Research Site

St Louis, Missouri, United States

Research Site

West Orange, New Jersey, United States

Research Site

New York, New York, United States

...and 23 more locations

Time frame: Extension study baseline and weeks 23 and 28

Percentage of Participants Who Achieved Mean iPTH ≤ 300 pg/mL During Weeks 23 and 28

For participants who had no values during week 23 and 28, the mean of the last 2 available post-baseline values collected in the dose-titration phase was used. If only 1 post-baseline value was available, this single value was used. If no post-baseline value was available, the participant was considered a non-responder. Data collected more than 7 days after the last dose of study drug were excluded.

Time frame: Weeks 23 and 28

Change From Baseline in Corrected Serum Calcium to the Mean Value During Weeks 23 to 28

For participants who had no values during weeks 23 to 28, the mean of the last 2 available post-baseline values collected in the dose-titration phase was used. If only 1 post-baseline value was available, this single value was used. If no post-baseline value was available, the participant was excluded from the analysis. Data collected more than 7 days after the last dose of study drug were excluded.

Time frame: Extension study baseline and weeks 23 and 28

Change From Baseline in Serum Phosphorus to the Mean Value During Weeks 23 to 28

Time frame: Extension study baseline and weeks 23 and 28

Serum Corrected Calcium at Baseline, Week 11, and Week 28

Data collected more than 7 days after the last dose of study drug were excluded.

Time frame: Extension study baseline, week 11 and week 28

Serum Phosphorus at Baseline, Week 11, and Week 28

Data collected more than 7 days after the last dose of study drug were excluded.

Time frame: Extension study baseline, week 11 and week 28

Percentage of Participants Achieving ≥ 30% Reduction in iPTH From Day 1 of Cinacalcet Treatment to Mean Value During Weeks 11 and 15

Time frame: Baseline and weeks 11 and 15, relative to day 1 of cinacalcet treatment.

Percentage of Participants Achieving ≥ 30% Reduction in iPTH From Day 1 of Cinacalcet Treatment to Mean Value During Weeks 23 and 28

The percentage of participants who achieved ≥ 30% reduction in iPTH measured from the date the initial dose of cinacalcet was administered, in parent study 20130356 or 20110100 for participants who received cinacalcet in the parent study, or in the extension study for participants who received SOC only in parent study 20130356. For participants who did not have an iPTH value during weeks 23 and 28, the mean of the last two available post-baseline values collected at protocol-specified visits was used. If only one post-baseline value was available, this single value was used. If no post-baseline value was available, the participant was considered a non-responder. Data collected more than 7 days after the last dose of study drug were excluded.

Time frame: Baseline and weeks 23 and 28, relative to day 1 of cinacalcet treatment.

Percent Change From Day 1 of Cinacalcet Treatment in iPTH Over Time

Percent change in iPTH measured from the date the initial dose of cinacalcet was administered, either in parent study 20130356 or 20110100, or in the extension study for participants who received SOC only in parent study 20130356. Data collected more than 7 days after the last dose of study drug were excluded.

Time frame: Baseline and weeks 3, 7, 11, 15, 17, 18, 19, 20, 23, 27, 31, 35, 39, 43, 48, 52, relative to day 1 of cinacalcet treatment, and at the end of treatment visit and end of study visit (4 weeks after the end of treatment visit).

Change From Day 1 of Cinacalcet Treatment in Serum Corrected Calcium Over Time

Change in corrected calcium measured from the date the initial dose of cinacalcet was administered, either in parent study 20130356 or 20110100, or in the extension study for participants who received SOC only in parent study 20130356. Data collected more than 7 days after the last dose of study drug were excluded.

Change From Day 1 of Cinacalcet Treatment in Serum Phosphorus Over Time

Change in phosphorus measured from the date the initial dose of cinacalcet was administered, either in parent study 20130356 or 20110100, or in the extension study for participants who received SOC only in parent study 20130356. Data collected more than 7 days after the last dose of study drug were excluded.