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Extension Study of Etelcalcetide in the Treatment of Secondary Hyperparathyroidism (SHPT) in Patients With Chronic Kidney Disease (CKD) on Hemodialysis

Primary Purpose

Hyperparathyroidism, Secondary

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Etelcalcetide
Sponsored by
Amgen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hyperparathyroidism, Secondary focused on measuring Secondary Hyperparathyroidism (SHPT), chronic kidney disease (CKD), hemodialysis, parathyroid hormone (PTH), hypocalcemia, bone and mineral metabolism

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Subject understands the study procedures and agrees to participate in the study by giving written informed consent.
  • Subject must complete the treatment and follow-up period, or have been discontinued for rising intact parathyroid hormone (iPTH), from an AMG 416 phase 3 parent study prior to the start of dosing in this study: 20120229 (NCT01785849), 20120230 (NCT01788046), or 20120359 (NCT01932970).
  • Subject agrees to not participate in another study of an investigational agent during the study.
  • Other Inclusion Criteria may apply

Exclusion Criteria:

  • Currently receiving treatment in another investigational device or drug study.
  • Currently receiving other investigational procedures while participating in this study.
  • Subject has known sensitivity to any of the products or components to be administered during dosing.
  • Subject has an unstable medical condition based on medical history, physical examination, and routine laboratory tests, or is otherwise unstable in the judgment of the Investigator.

Other Exclusion Criteria may apply

Sites / Locations

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Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Etelcalcetide

Arm Description

Participants received etelcalcetide at a starting dose of 5 mg three times a week (TIW) for up to 52 weeks. Etelcalcetide dose could be increased at weeks 5, 9, 17, 25, 33, 41, and 49 to a maximum dose of 15 mg to achieve predialysis serum parathyroid hormone levels ≤ 300 pg/mL.

Outcomes

Primary Outcome Measures

Number of Participants With Adverse Events (AEs)
Treatment-related adverse events are those the investigator indicated as having a reasonable possibility of having been caused by etelcalcetide. A serious adverse event is defined as an adverse event that meets at least 1 of the following serious criteria: • fatal • life threatening • requires in-patient hospitalization or prolongation of existing hospitalization • results in persistent or significant disability/incapacity • congenital anomaly/birth defect • other medically important serious event.
Number of Participants With Shift in Laboratory Values From Baseline Grade 0 or 1 to Post-baseline Grade 3 or 4
Laboratory toxicity grading was based on Common Terminology Criteria for Adverse Events (CTCAE) version 4.0, where Grade 0 represents values in the normal range and grade 4 represents values with life-threatening consequences and urgent intervention indicated.
Number of Participants Who Developed Anti-etelcalcetide Antibodies
A validated dual flow-cell biosensor immunoassay was used to detect antibodies capable of binding etelcalcetide. The number of participants with a negative or no result at baseline and positive binding antibodies at any time post-baseline is reported.
Change From Baseline in Blood Pressure
Blood pressure (BP) values were taken post-hemodialysis assessments.

Secondary Outcome Measures

Percentage of Participants With > 30% Reduction From Baseline in PTH During the Efficacy Assessment Phase
The efficacy assessment phase (EAP) is defined as the last 6 weeks before ending treatment, which was only for participants who completed a minimum of 8 weeks of treatment with etelcalcetide. If multiple assessments were available during the EAP, values were averaged.
Percentage of Participants With > 30% Reduction From Baseline in PTH During the EAP12
The efficacy assessment phase at 12 months (EAP12) was defined as the period from week 46 to 53 (inclusive). If multiple assessments were available during the EAP12, values were averaged.
Percentage of Participants With PTH ≤ 300 pg/mL During the EAP
Percentage of Participants With PTH ≤ 300 pg/mL During the EAP12
Percent Change From Baseline in Mean PTH During the EAP
Percent Change From Baseline in Mean PTH During the EAP12
Percent Change From Baseline in Mean Corrected Calcium During the EAP
Percent Change From Baseline in Mean Corrected Calcium During the EAP12
Percent Change From Baseline in Mean Corrected Calcium Phosphorus Product During the EAP
Percent Change From Baseline in Mean Corrected Calcium Phosphorus Product During the EAP12
Percent Change From Baseline in Mean Phosphorus During the EAP
Percent Change From Baseline in Mean Phosphorus During the EAP12

Full Information

First Posted
February 5, 2013
Last Updated
April 1, 2019
Sponsor
Amgen
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1. Study Identification

Unique Protocol Identification Number
NCT01785875
Brief Title
Extension Study of Etelcalcetide in the Treatment of Secondary Hyperparathyroidism (SHPT) in Patients With Chronic Kidney Disease (CKD) on Hemodialysis
Official Title
A Multicenter Single-arm Extension Study to Describe the Long-term Efficacy and Safety of AMG 416 in the Treatment of Secondary Hyperparathyroidism in Subjects With Chronic Kidney Disease on Hemodialysis
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
July 31, 2013 (Actual)
Primary Completion Date
July 1, 2015 (Actual)
Study Completion Date
July 1, 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Amgen

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study is designed to describe the long-term safety and efficacy of etelcalcetide (AMG 416) for the treatment of SHPT in adults with CKD on hemodialysis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hyperparathyroidism, Secondary
Keywords
Secondary Hyperparathyroidism (SHPT), chronic kidney disease (CKD), hemodialysis, parathyroid hormone (PTH), hypocalcemia, bone and mineral metabolism

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
891 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Etelcalcetide
Arm Type
Experimental
Arm Description
Participants received etelcalcetide at a starting dose of 5 mg three times a week (TIW) for up to 52 weeks. Etelcalcetide dose could be increased at weeks 5, 9, 17, 25, 33, 41, and 49 to a maximum dose of 15 mg to achieve predialysis serum parathyroid hormone levels ≤ 300 pg/mL.
Intervention Type
Drug
Intervention Name(s)
Etelcalcetide
Other Intervention Name(s)
AMG 416
Intervention Description
Administered by bolus injection into the venous line of the dialysis circuit at the end of hemodialysis treatment, and prior to or during rinse-back with each hemodialysis session (ie, 3 times per week).
Primary Outcome Measure Information:
Title
Number of Participants With Adverse Events (AEs)
Description
Treatment-related adverse events are those the investigator indicated as having a reasonable possibility of having been caused by etelcalcetide. A serious adverse event is defined as an adverse event that meets at least 1 of the following serious criteria: • fatal • life threatening • requires in-patient hospitalization or prolongation of existing hospitalization • results in persistent or significant disability/incapacity • congenital anomaly/birth defect • other medically important serious event.
Time Frame
From first dose until 30 days after last dose; the treatment period was 52 weeks.
Title
Number of Participants With Shift in Laboratory Values From Baseline Grade 0 or 1 to Post-baseline Grade 3 or 4
Description
Laboratory toxicity grading was based on Common Terminology Criteria for Adverse Events (CTCAE) version 4.0, where Grade 0 represents values in the normal range and grade 4 represents values with life-threatening consequences and urgent intervention indicated.
Time Frame
52 weeks
Title
Number of Participants Who Developed Anti-etelcalcetide Antibodies
Description
A validated dual flow-cell biosensor immunoassay was used to detect antibodies capable of binding etelcalcetide. The number of participants with a negative or no result at baseline and positive binding antibodies at any time post-baseline is reported.
Time Frame
Baseline, Week 12, Week 24, Week 36, Week 53, the 30-day follow-up visit
Title
Change From Baseline in Blood Pressure
Description
Blood pressure (BP) values were taken post-hemodialysis assessments.
Time Frame
Baseline and Weeks 24 and 48
Secondary Outcome Measure Information:
Title
Percentage of Participants With > 30% Reduction From Baseline in PTH During the Efficacy Assessment Phase
Description
The efficacy assessment phase (EAP) is defined as the last 6 weeks before ending treatment, which was only for participants who completed a minimum of 8 weeks of treatment with etelcalcetide. If multiple assessments were available during the EAP, values were averaged.
Time Frame
Baseline and the efficacy assessment phase, defined as the last 6 weeks prior to ending treatment for participants who completed a minimum of 8 weeks of treatment (weeks 46-52 for participants who completed 52 weeks of treatment)
Title
Percentage of Participants With > 30% Reduction From Baseline in PTH During the EAP12
Description
The efficacy assessment phase at 12 months (EAP12) was defined as the period from week 46 to 53 (inclusive). If multiple assessments were available during the EAP12, values were averaged.
Time Frame
Baseline and the efficacy assessment phase at month 12 (weeks 46-53)
Title
Percentage of Participants With PTH ≤ 300 pg/mL During the EAP
Time Frame
Baseline and the efficacy assessment phase
Title
Percentage of Participants With PTH ≤ 300 pg/mL During the EAP12
Time Frame
Week 46 to 53
Title
Percent Change From Baseline in Mean PTH During the EAP
Time Frame
Baseline and the efficacy assessment phase
Title
Percent Change From Baseline in Mean PTH During the EAP12
Time Frame
Baseline and the efficacy assessment phase at month 12 (weeks 46-53)
Title
Percent Change From Baseline in Mean Corrected Calcium During the EAP
Time Frame
Baseline and the efficacy assessment phase
Title
Percent Change From Baseline in Mean Corrected Calcium During the EAP12
Time Frame
Baseline and the efficacy assessment phase at month 12 (weeks 46-53)
Title
Percent Change From Baseline in Mean Corrected Calcium Phosphorus Product During the EAP
Time Frame
Baseline and the efficacy assessment phase
Title
Percent Change From Baseline in Mean Corrected Calcium Phosphorus Product During the EAP12
Time Frame
Baseline and the efficacy assessment phase at month 12 (weeks 46-53)
Title
Percent Change From Baseline in Mean Phosphorus During the EAP
Time Frame
Baseline and the efficacy assessment phase
Title
Percent Change From Baseline in Mean Phosphorus During the EAP12
Time Frame
Baseline and the efficacy assessment phase at month 12 (weeks 46-53)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subject understands the study procedures and agrees to participate in the study by giving written informed consent. Subject must complete the treatment and follow-up period, or have been discontinued for rising intact parathyroid hormone (iPTH), from an AMG 416 phase 3 parent study prior to the start of dosing in this study: 20120229 (NCT01785849), 20120230 (NCT01788046), or 20120359 (NCT01932970). Subject agrees to not participate in another study of an investigational agent during the study. Other Inclusion Criteria may apply Exclusion Criteria: Currently receiving treatment in another investigational device or drug study. Currently receiving other investigational procedures while participating in this study. Subject has known sensitivity to any of the products or components to be administered during dosing. Subject has an unstable medical condition based on medical history, physical examination, and routine laboratory tests, or is otherwise unstable in the judgment of the Investigator. Other Exclusion Criteria may apply
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
MD
Organizational Affiliation
Amgen
Official's Role
Study Director
Facility Information:
Facility Name
Research Site
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35211
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United States
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Research Site
City
Pine Bluff
State/Province
Arkansas
ZIP/Postal Code
71603
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United States
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Azusa
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California
ZIP/Postal Code
91702
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United States
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Bakersfield
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California
ZIP/Postal Code
93308
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United States
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Chula Vista
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California
ZIP/Postal Code
91910
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United States
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Cudahy
State/Province
California
ZIP/Postal Code
90201
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United States
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Research Site
City
Fairfield
State/Province
California
ZIP/Postal Code
94534
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United States
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Research Site
City
Glendale
State/Province
California
ZIP/Postal Code
91205
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United States
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Research Site
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Los Angeles
State/Province
California
ZIP/Postal Code
90022
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United States
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Research Site
City
Los Angeles
State/Province
California
ZIP/Postal Code
90025
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United States
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Research Site
City
Los Angeles
State/Province
California
ZIP/Postal Code
90048
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United States
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Research Site
City
Lynwood
State/Province
California
ZIP/Postal Code
90262
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United States
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Research Site
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Northridge
State/Province
California
ZIP/Postal Code
91324
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United States
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Research Site
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Norwalk
State/Province
California
ZIP/Postal Code
90650
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United States
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Research Site
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Ontario
State/Province
California
ZIP/Postal Code
91762
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United States
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Research Site
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Riverside
State/Province
California
ZIP/Postal Code
92501
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United States
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San Gabriel
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California
ZIP/Postal Code
91776
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United States
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Simi Valley
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California
ZIP/Postal Code
93065
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United States
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Whittier
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California
ZIP/Postal Code
90603
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United States
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Research Site
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Arvada
State/Province
Colorado
ZIP/Postal Code
80002
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United States
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Denver
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Colorado
ZIP/Postal Code
80230
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United States
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Stamford
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Connecticut
ZIP/Postal Code
06902
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United States
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Coral Springs
State/Province
Florida
ZIP/Postal Code
33071
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United States
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Lauderdale Lakes
State/Province
Florida
ZIP/Postal Code
33313
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United States
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Miami
State/Province
Florida
ZIP/Postal Code
33150
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United States
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Research Site
City
Miami
State/Province
Florida
ZIP/Postal Code
33173
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United States
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Research Site
City
Ocala
State/Province
Florida
ZIP/Postal Code
34471
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United States
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Research Site
City
Pembroke Pines
State/Province
Florida
ZIP/Postal Code
33025
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United States
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Research Site
City
Pinecrest
State/Province
Florida
ZIP/Postal Code
33156
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United States
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Research Site
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Tampa
State/Province
Florida
ZIP/Postal Code
33614
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United States
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Research Site
City
Augusta
State/Province
Georgia
ZIP/Postal Code
30901
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United States
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Research Site
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Macon
State/Province
Georgia
ZIP/Postal Code
31217
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United States
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Meridian
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Idaho
ZIP/Postal Code
83642
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United States
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Evanston
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Illinois
ZIP/Postal Code
60201
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United States
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Gurnee
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Illinois
ZIP/Postal Code
60031
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United States
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Merrillville
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Indiana
ZIP/Postal Code
46410
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United States
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Michigan City
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Indiana
ZIP/Postal Code
46360
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United States
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Wichita
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Kansas
ZIP/Postal Code
67214-2998
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United States
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Baton Rouge
State/Province
Louisiana
ZIP/Postal Code
70808
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United States
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Lafayette
State/Province
Louisiana
ZIP/Postal Code
70503
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United States
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Shreveport
State/Province
Louisiana
ZIP/Postal Code
71101
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United States
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Springfield
State/Province
Massachusetts
ZIP/Postal Code
01107
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United States
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Detroit
State/Province
Michigan
ZIP/Postal Code
48202
Country
United States
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Research Site
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48236
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United States
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Research Site
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Kalamazoo
State/Province
Michigan
ZIP/Postal Code
49007
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United States
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Research Site
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Pontiac
State/Province
Michigan
ZIP/Postal Code
48341
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United States
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Research Site
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Brookhaven
State/Province
Mississippi
ZIP/Postal Code
39601
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United States
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Columbus
State/Province
Mississippi
ZIP/Postal Code
39705
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United States
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Gulfport
State/Province
Mississippi
ZIP/Postal Code
39501
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United States
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Research Site
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Tupelo
State/Province
Mississippi
ZIP/Postal Code
38801
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United States
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Research Site
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Kansas City
State/Province
Missouri
ZIP/Postal Code
64111
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United States
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Research Site
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Saint Louis
State/Province
Missouri
ZIP/Postal Code
63136
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United States
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Research Site
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Lincoln
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Nebraska
ZIP/Postal Code
68510
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United States
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Research Site
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Las Vegas
State/Province
Nevada
ZIP/Postal Code
89106
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United States
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Research Site
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Reno
State/Province
Nevada
ZIP/Postal Code
89511
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United States
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Research Site
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Portsmouth
State/Province
New Hampshire
ZIP/Postal Code
03801
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United States
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Research Site
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Eatontown
State/Province
New Jersey
ZIP/Postal Code
07724
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United States
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Research Site
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Bronx
State/Province
New York
ZIP/Postal Code
10461
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United States
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Research Site
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Brooklyn
State/Province
New York
ZIP/Postal Code
11212
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United States
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Research Site
City
Brooklyn
State/Province
New York
ZIP/Postal Code
11235
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United States
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Research Site
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Great Neck
State/Province
New York
ZIP/Postal Code
11021
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United States
Facility Name
Research Site
City
Orchard Park
State/Province
New York
ZIP/Postal Code
14127
Country
United States
Facility Name
Research Site
City
Ridgewood
State/Province
New York
ZIP/Postal Code
11385
Country
United States
Facility Name
Research Site
City
Rosedale
State/Province
New York
ZIP/Postal Code
11422
Country
United States
Facility Name
Research Site
City
Yonkers
State/Province
New York
ZIP/Postal Code
10704
Country
United States
Facility Name
Research Site
City
Carrboro
State/Province
North Carolina
ZIP/Postal Code
27510
Country
United States
Facility Name
Research Site
City
Charlotte
State/Province
North Carolina
ZIP/Postal Code
28207
Country
United States
Facility Name
Research Site
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27704
Country
United States
Facility Name
Research Site
City
New Bern
State/Province
North Carolina
ZIP/Postal Code
28562
Country
United States
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Research Site
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45206
Country
United States
Facility Name
Research Site
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73116
Country
United States
Facility Name
Research Site
City
Bethlehem
State/Province
Pennsylvania
ZIP/Postal Code
18017
Country
United States
Facility Name
Research Site
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19106
Country
United States
Facility Name
Research Site
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19118
Country
United States
Facility Name
Research Site
City
Columbia
State/Province
South Carolina
ZIP/Postal Code
29203
Country
United States
Facility Name
Research Site
City
Orangeburg
State/Province
South Carolina
ZIP/Postal Code
29118
Country
United States
Facility Name
Research Site
City
Chattanooga
State/Province
Tennessee
ZIP/Postal Code
37408
Country
United States
Facility Name
Research Site
City
Columbia
State/Province
Tennessee
ZIP/Postal Code
38401
Country
United States
Facility Name
Research Site
City
Knoxville
State/Province
Tennessee
ZIP/Postal Code
37923
Country
United States
Facility Name
Research Site
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37205
Country
United States
Facility Name
Research Site
City
Arlington
State/Province
Texas
ZIP/Postal Code
76015
Country
United States
Facility Name
Research Site
City
Austin
State/Province
Texas
ZIP/Postal Code
78758
Country
United States
Facility Name
Research Site
City
Edinburg
State/Province
Texas
ZIP/Postal Code
78539
Country
United States
Facility Name
Research Site
City
Fort Worth
State/Province
Texas
ZIP/Postal Code
76104
Country
United States
Facility Name
Research Site
City
Fort Worth
State/Province
Texas
ZIP/Postal Code
76105
Country
United States
Facility Name
Research Site
City
Fort Worth
State/Province
Texas
ZIP/Postal Code
76164
Country
United States
Facility Name
Research Site
City
Grand Prairie
State/Province
Texas
ZIP/Postal Code
75050
Country
United States
Facility Name
Research Site
City
Houston
State/Province
Texas
ZIP/Postal Code
77004
Country
United States
Facility Name
Research Site
City
Houston
State/Province
Texas
ZIP/Postal Code
77054
Country
United States
Facility Name
Research Site
City
Lubbock
State/Province
Texas
ZIP/Postal Code
79430
Country
United States
Facility Name
Research Site
City
Mansfield
State/Province
Texas
ZIP/Postal Code
76063
Country
United States
Facility Name
Research Site
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78205
Country
United States
Facility Name
Research Site
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78215
Country
United States
Facility Name
Research Site
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78229
Country
United States
Facility Name
Research Site
City
Alexandria
State/Province
Virginia
ZIP/Postal Code
22304
Country
United States
Facility Name
Research Site
City
Alexandria
State/Province
Virginia
ZIP/Postal Code
22306
Country
United States
Facility Name
Research Site
City
Fairfax
State/Province
Virginia
ZIP/Postal Code
22033
Country
United States
Facility Name
Research Site
City
Hampton
State/Province
Virginia
ZIP/Postal Code
23666
Country
United States
Facility Name
Research Site
City
Mechanicsville
State/Province
Virginia
ZIP/Postal Code
23116
Country
United States
Facility Name
Research Site
City
Norfolk
State/Province
Virginia
ZIP/Postal Code
23502
Country
United States
Facility Name
Research Site
City
Bluefield
State/Province
West Virginia
ZIP/Postal Code
24701
Country
United States
Facility Name
Research Site
City
Liverpool
State/Province
New South Wales
ZIP/Postal Code
2170
Country
Australia
Facility Name
Research Site
City
St Leonards
State/Province
New South Wales
ZIP/Postal Code
2065
Country
Australia
Facility Name
Research Site
City
Westmead
State/Province
New South Wales
ZIP/Postal Code
2145
Country
Australia
Facility Name
Research Site
City
Brisbane
State/Province
Queensland
ZIP/Postal Code
4102
Country
Australia
Facility Name
Research Site
City
Adelaide
State/Province
South Australia
ZIP/Postal Code
5000
Country
Australia
Facility Name
Research Site
City
Clayton
State/Province
Victoria
ZIP/Postal Code
3168
Country
Australia
Facility Name
Research Site
City
Parkville
State/Province
Victoria
ZIP/Postal Code
3050
Country
Australia
Facility Name
Research Site
City
Graz
ZIP/Postal Code
8036
Country
Austria
Facility Name
Research Site
City
Linz
ZIP/Postal Code
4010
Country
Austria
Facility Name
Research Site
City
Wien
ZIP/Postal Code
1090
Country
Austria
Facility Name
Research Site
City
Aalst
ZIP/Postal Code
9300
Country
Belgium
Facility Name
Research Site
City
Baudour
ZIP/Postal Code
7331
Country
Belgium
Facility Name
Research Site
City
Bonheiden
ZIP/Postal Code
2820
Country
Belgium
Facility Name
Research Site
City
Brussels
ZIP/Postal Code
1200
Country
Belgium
Facility Name
Research Site
City
Brussel
ZIP/Postal Code
1090
Country
Belgium
Facility Name
Research Site
City
Bruxelles
ZIP/Postal Code
1020
Country
Belgium
Facility Name
Research Site
City
Leuven
ZIP/Postal Code
3000
Country
Belgium
Facility Name
Research Site
City
Liege
ZIP/Postal Code
4000
Country
Belgium
Facility Name
Research Site
City
Liège
ZIP/Postal Code
4000
Country
Belgium
Facility Name
Research Site
City
Roeselare
ZIP/Postal Code
8800
Country
Belgium
Facility Name
Research Site
City
Tournai
ZIP/Postal Code
7500
Country
Belgium
Facility Name
Research Site
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T6G 2B7
Country
Canada
Facility Name
Research Site
City
Brampton
State/Province
Ontario
ZIP/Postal Code
L6R 3J7
Country
Canada
Facility Name
Research Site
City
Greenfield Park
State/Province
Quebec
ZIP/Postal Code
J4V 2H1
Country
Canada
Facility Name
Research Site
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H1T 2M4
Country
Canada
Facility Name
Research Site
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H4J 1C5
Country
Canada
Facility Name
Research Site
City
Hradec Kralove
ZIP/Postal Code
500 05
Country
Czechia
Facility Name
Research Site
City
Novy Jicin
ZIP/Postal Code
741 01
Country
Czechia
Facility Name
Research Site
City
Plzen
ZIP/Postal Code
301 00
Country
Czechia
Facility Name
Research Site
City
Praha 4 - Nusle
ZIP/Postal Code
140 00
Country
Czechia
Facility Name
Research Site
City
Praha 4
ZIP/Postal Code
140 21
Country
Czechia
Facility Name
Research Site
City
Praha 6
ZIP/Postal Code
169 00
Country
Czechia
Facility Name
Research Site
City
Slavkov u Brna
ZIP/Postal Code
684 01
Country
Czechia
Facility Name
Research Site
City
Usti nad Orlici
ZIP/Postal Code
562 18
Country
Czechia
Facility Name
Research Site
City
Bordeaux Cedex
ZIP/Postal Code
33076
Country
France
Facility Name
Research Site
City
Caen
ZIP/Postal Code
14000
Country
France
Facility Name
Research Site
City
La Tronche cedex
ZIP/Postal Code
38701
Country
France
Facility Name
Research Site
City
Marseille cedex 5
ZIP/Postal Code
13385
Country
France
Facility Name
Research Site
City
Marseille
ZIP/Postal Code
13253
Country
France
Facility Name
Research Site
City
Poitiers
ZIP/Postal Code
86021
Country
France
Facility Name
Research Site
City
Reims Cedex
ZIP/Postal Code
51092
Country
France
Facility Name
Research Site
City
Saint-Ouen
ZIP/Postal Code
93400
Country
France
Facility Name
Research Site
City
Berlin
ZIP/Postal Code
12053
Country
Germany
Facility Name
Research Site
City
Dresden
ZIP/Postal Code
01307
Country
Germany
Facility Name
Research Site
City
Erfurt
ZIP/Postal Code
99089
Country
Germany
Facility Name
Research Site
City
Villingen-Schwenningen
ZIP/Postal Code
78052
Country
Germany
Facility Name
Research Site
City
Baja
ZIP/Postal Code
6500
Country
Hungary
Facility Name
Research Site
City
Budapest
ZIP/Postal Code
1037
Country
Hungary
Facility Name
Research Site
City
Budapest
ZIP/Postal Code
1076
Country
Hungary
Facility Name
Research Site
City
Budapest
ZIP/Postal Code
1106
Country
Hungary
Facility Name
Research Site
City
Esztergom
ZIP/Postal Code
2500
Country
Hungary
Facility Name
Research Site
City
Gyor
ZIP/Postal Code
9023
Country
Hungary
Facility Name
Research Site
City
Kaposvar
ZIP/Postal Code
7400
Country
Hungary
Facility Name
Research Site
City
Kecskemet
ZIP/Postal Code
6000
Country
Hungary
Facility Name
Research Site
City
Miskolc
ZIP/Postal Code
3526
Country
Hungary
Facility Name
Research Site
City
Pecs
ZIP/Postal Code
7624
Country
Hungary
Facility Name
Research Site
City
Zalaegerszeg
ZIP/Postal Code
8900
Country
Hungary
Facility Name
Research Site
City
Ashkelon
ZIP/Postal Code
78278
Country
Israel
Facility Name
Research Site
City
Jerusalem
ZIP/Postal Code
91120
Country
Israel
Facility Name
Research Site
City
Kfar-Saba
ZIP/Postal Code
44281
Country
Israel
Facility Name
Research Site
City
Nahariya
ZIP/Postal Code
22100
Country
Israel
Facility Name
Research Site
City
Tel Aviv
ZIP/Postal Code
64239
Country
Israel
Facility Name
Research Site
City
Tel Hashomer
ZIP/Postal Code
52621
Country
Israel
Facility Name
Research Site
City
Zerifin
ZIP/Postal Code
70300
Country
Israel
Facility Name
Research Site
City
Ancona
ZIP/Postal Code
60131
Country
Italy
Facility Name
Research Site
City
Lecco
ZIP/Postal Code
23900
Country
Italy
Facility Name
Research Site
City
Milano
ZIP/Postal Code
20122
Country
Italy
Facility Name
Research Site
City
Milano
ZIP/Postal Code
20142
Country
Italy
Facility Name
Research Site
City
Pavia
ZIP/Postal Code
27100
Country
Italy
Facility Name
Research Site
City
Verona
ZIP/Postal Code
37126
Country
Italy
Facility Name
Research Site
City
Amsterdam
ZIP/Postal Code
1081 HV
Country
Netherlands
Facility Name
Research Site
City
Enschede
ZIP/Postal Code
7511 JX
Country
Netherlands
Facility Name
Research Site
City
Rotterdam
ZIP/Postal Code
3079 DZ
Country
Netherlands
Facility Name
Research Site
City
Venlo
ZIP/Postal Code
5912 BL
Country
Netherlands
Facility Name
Research Site
City
Bialystok
ZIP/Postal Code
15-540
Country
Poland
Facility Name
Research Site
City
Gdansk
ZIP/Postal Code
80-952
Country
Poland
Facility Name
Research Site
City
Golub-Dobrzyn
ZIP/Postal Code
87-400
Country
Poland
Facility Name
Research Site
City
Krakow
ZIP/Postal Code
31-501
Country
Poland
Facility Name
Research Site
City
Lodz
ZIP/Postal Code
90-153
Country
Poland
Facility Name
Research Site
City
Rybnik
ZIP/Postal Code
44-200
Country
Poland
Facility Name
Research Site
City
Warszawa
ZIP/Postal Code
02-006
Country
Poland
Facility Name
Research Site
City
Warszawa
ZIP/Postal Code
02-097
Country
Poland
Facility Name
Research Site
City
Warszawa
ZIP/Postal Code
04-749
Country
Poland
Facility Name
Research Site
City
Zamosc
ZIP/Postal Code
87-100
Country
Poland
Facility Name
Research Site
City
Moscow
ZIP/Postal Code
123183
Country
Russian Federation
Facility Name
Research Site
City
Saint Petersburg
ZIP/Postal Code
191104
Country
Russian Federation
Facility Name
Research Site
City
Saint Petersburg
ZIP/Postal Code
196247
Country
Russian Federation
Facility Name
Research Site
City
Saint Petersburg
ZIP/Postal Code
197110
Country
Russian Federation
Facility Name
Research Site
City
Saint Petersburg
ZIP/Postal Code
198510
Country
Russian Federation
Facility Name
Research Site
City
Saint-Petersburg
ZIP/Postal Code
195067
Country
Russian Federation
Facility Name
Research Site
City
Saint-Petersburg
ZIP/Postal Code
195257
Country
Russian Federation
Facility Name
Research Site
City
Yaroslavl
ZIP/Postal Code
150062
Country
Russian Federation
Facility Name
Research Site
City
Cordoba
State/Province
Andalucía
ZIP/Postal Code
14004
Country
Spain
Facility Name
Research Site
City
Santander
State/Province
Cantabria
ZIP/Postal Code
39008
Country
Spain
Facility Name
Research Site
City
Barcelona
State/Province
Cataluña
ZIP/Postal Code
08003
Country
Spain
Facility Name
Research Site
City
Barcelona
State/Province
Cataluña
ZIP/Postal Code
08025
Country
Spain
Facility Name
Research Site
City
Barcelona
State/Province
Cataluña
ZIP/Postal Code
08035
Country
Spain
Facility Name
Research Site
City
Barcelona
State/Province
Cataluña
ZIP/Postal Code
08036
Country
Spain
Facility Name
Research Site
City
Majadahonda
State/Province
Madrid
ZIP/Postal Code
28222
Country
Spain
Facility Name
Research Site
City
Madrid
ZIP/Postal Code
28041
Country
Spain
Facility Name
Research Site
City
Karlstad
ZIP/Postal Code
651 85
Country
Sweden
Facility Name
Research Site
City
Stockholm
ZIP/Postal Code
141 86
Country
Sweden
Facility Name
Research Site
City
Uppsala
ZIP/Postal Code
751 85
Country
Sweden
Facility Name
Research Site
City
Cambridge
ZIP/Postal Code
CB2 2QQ
Country
United Kingdom
Facility Name
Research Site
City
Coventry
ZIP/Postal Code
CV2 2DX
Country
United Kingdom
Facility Name
Research Site
City
London
ZIP/Postal Code
NW3 2QG
Country
United Kingdom
Facility Name
Research Site
City
Nottingham
ZIP/Postal Code
NG5 1PB
Country
United Kingdom
Facility Name
Research Site
City
Sheffield
ZIP/Postal Code
S5 7AU
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
30875390
Citation
Block GA, Chertow GM, Sullivan JT, Deng H, Mather O, Tomlin H, Serenko M. An integrated analysis of safety and tolerability of etelcalcetide in patients receiving hemodialysis with secondary hyperparathyroidism. PLoS One. 2019 Mar 15;14(3):e0213774. doi: 10.1371/journal.pone.0213774. eCollection 2019.
Results Reference
background
PubMed Identifier
30859218
Citation
Bushinsky DA, Chertow GM, Cheng S, Deng H, Kopyt N, Martin KJ, Rastogi A, Urena-Torres P, Vervloet M, Block GA. One-year safety and efficacy of intravenous etelcalcetide in patients on hemodialysis with secondary hyperparathyroidism. Nephrol Dial Transplant. 2020 Oct 1;35(10):1769-1778. doi: 10.1093/ndt/gfz039. Erratum In: Nephrol Dial Transplant. 2019 May 15;:1642.
Results Reference
derived
Links:
URL
http://www.amgentrials.com
Description
AmgenTrials clinical trials website

Learn more about this trial

Extension Study of Etelcalcetide in the Treatment of Secondary Hyperparathyroidism (SHPT) in Patients With Chronic Kidney Disease (CKD) on Hemodialysis

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