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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT01277510




Registration number
NCT01277510
Ethics application status
Date submitted
13/01/2011
Date registered
17/01/2011
Date last updated
29/06/2020

Titles & IDs
Public title
Pediatric Chronic Kidney Disease Safety and Efficacy
Scientific title
A Randomized, Double-blind, Placebo Controlled Study to Assess the Efficacy and Safety of Cinacalcet HCl in Pediatric Subjects With Chronic Kidney Disease and Secondary Hyperparathyroidism Receiving Dialysis
Secondary ID [1] 0 0
20070208
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Chronic Kidney Disease 0 0
Hyperparathyroidism 0 0
Hyperparathyroidism, Secondary 0 0
Kidney Disease 0 0
Secondary Hyperparathyroidism 0 0
Condition category
Condition code
Renal and Urogenital 0 0 0 0
Kidney disease
Renal and Urogenital 0 0 0 0
Other renal and urogenital disorders
Metabolic and Endocrine 0 0 0 0
Other endocrine disorders

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - cinacalcet capsule
Treatment: Drugs - placebo
Treatment: Drugs - Standard of Care

Placebo comparator: Placebo - Participants received standard of care and placebo once daily for 30 weeks during the double-blind phase. During the open-label phase, participants received cinacalcet with standard of care for an additional 30 weeks. The starting dose of cinacalcet was = 0.20 mg/kg based on dry weight, and could be titrated up according to plasma iPTH and serum calcium levels every 4 weeks up to Week 54 to a maximum dose of 4.2 mg/kg.

Experimental: Cinacalcet - Participants received standard of care and cinacalcet once daily for 30 weeks during the double-blind phase. The starting dose of cinacalcet was = 0.20 mg/kg based on dry weight, and could be titrated up according to plasma iPTH and serum calcium levels every 4 weeks until Week 24 to a maximum dose of 4.2 mg/kg. During the open-label phase participants continued to receive cinacalcet with standard of care for an additional 30 weeks.


Treatment: Drugs: cinacalcet capsule
Cinacalcet was prepared for oral administration as both capsules for sprinkling and film coated tablets for swallowing.

Treatment: Drugs: placebo
Placebo tablets and capsules for sprinkling identical to active treatment.

Treatment: Drugs: Standard of Care
All participants, regardless of treatment assignment, will receive standard of care with vitamin D sterols (calcitriol and its analogs), as prescribed by the treating physician.

Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Percentage of Participants Achieving = 30% Reduction in Mean iPTH From Baseline to the Efficacy Assessment Phase
Timepoint [1] 0 0
From Baseline to the Efficacy Assessment Phase, Weeks 25-30
Secondary outcome [1] 0 0
Percentage of Participants Achieving Mean iPTH = 300 pg/mL (31.8 Pmol/L) During the Efficacy Assessment Phase
Timepoint [1] 0 0
From Baseline to the Efficacy Assessment Phase (EAP), Weeks 25-30
Secondary outcome [2] 0 0
Percent Change From Baseline in Mean Corrected Total Serum Calcium During the Efficacy Assessment Period
Timepoint [2] 0 0
From Baseline to the Efficacy Assessment Phase, Weeks 25-30.
Secondary outcome [3] 0 0
Percent Change From Baseline in Mean Serum Phosphorus During the Efficacy Assessment Phase
Timepoint [3] 0 0
From Baseline to the Efficacy Assessment Phase, Weeks 25-30.
Secondary outcome [4] 0 0
Percent Change From Baseline in Mean Phosphorous Product (Ca x P) During the Efficacy Assessment Phase
Timepoint [4] 0 0
From Baseline to end of Efficacy Assessment Period, assessed up to 30 weeks
Secondary outcome [5] 0 0
Growth Velocity From Baseline to End of Double-blind Phase
Timepoint [5] 0 0
From Baseline to end of Efficacy Assessment at Week 30
Secondary outcome [6] 0 0
Growth Velocity From End of Double-blind Phase to End of Open-label Phase
Timepoint [6] 0 0
End of double-blind phase (Week 30) until end of the open-label phase (Week 60)
Secondary outcome [7] 0 0
Percent Change From Baseline in Mean Ionized Calcium During the Efficacy Assessment Phase
Timepoint [7] 0 0
From Baseline to the Efficacy Assessment Phase, Weeks 25-30.

Eligibility
Key inclusion criteria
* Age 6 to less than 18 years at screening
* Diagnosed with CKD and SHPT receiving hemodialysis or peritoneal dialysis for = 2 months before randomization
* Dry weight = 12.5 kg at screening
* iPTH obtained from the central laboratory must be > 300 pg/mL (31.8 pmol/L)
* Serum calcium (corrected) obtained from the central laboratory must be = 8.8 mg/dL (2.2 mmol/L)
* Serum phosphorus obtained from the central laboratory = 4.0 mg/dL (1.3 mmol/L) for children 6 to less than 12 years old, or = 3.5 mg/dL (1.1 mmol/L) for children 12 to less than 18 years old
* Subjects already receiving vitamin D sterols (either calcitriol or a synthetic analog), a stable dose within the last 2 months prior to randomization
* Subjects taking growth hormone, a stable dose defined as no change > than 20% in the last 2 months prior to randomization
* Subjects on anti-convulsant medication must be on a stable dose for 3 months, and have a therapeutic blood level of the anti-convulsant at the time of randomization
* Subjects must be on a dialysate calcium concentration of = 2.5 mEq/L (1.25 mmol/L) for at least 2 months prior to randomization
Minimum age
6 Years
Maximum age
17 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* Underwent parathyroidectomy in the last 6 months
* Anticipated parathyroidectomy within 6 months after randomization
* Received therapy with cinacalcet (sensipar/mimpara) within the last month
* A new onset of seizure or worsening of a pre-existing seizure disorder within the last 3 months
* Scheduled date for kidney transplant from a known living donor that makes completion of the study unlikely

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 3
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Stopped early
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
NSW,QLD,VIC
Recruitment hospital [1] 0 0
Research Site - Randwick
Recruitment hospital [2] 0 0
Research Site - Westmead
Recruitment hospital [3] 0 0
Research Site - Herston
Recruitment hospital [4] 0 0
Research Site - Parkville
Recruitment postcode(s) [1] 0 0
2031 - Randwick
Recruitment postcode(s) [2] 0 0
2145 - Westmead
Recruitment postcode(s) [3] 0 0
4029 - Herston
Recruitment postcode(s) [4] 0 0
3052 - Parkville
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Alabama
Country [2] 0 0
United States of America
State/province [2] 0 0
California
Country [3] 0 0
United States of America
State/province [3] 0 0
Florida
Country [4] 0 0
United States of America
State/province [4] 0 0
Maryland
Country [5] 0 0
United States of America
State/province [5] 0 0
Massachusetts
Country [6] 0 0
United States of America
State/province [6] 0 0
Missouri
Country [7] 0 0
United States of America
State/province [7] 0 0
New Jersey
Country [8] 0 0
United States of America
State/province [8] 0 0
New York
Country [9] 0 0
United States of America
State/province [9] 0 0
North Carolina
Country [10] 0 0
United States of America
State/province [10] 0 0
Ohio
Country [11] 0 0
United States of America
State/province [11] 0 0
Oregon
Country [12] 0 0
United States of America
State/province [12] 0 0
Pennsylvania
Country [13] 0 0
United States of America
State/province [13] 0 0
Texas
Country [14] 0 0
United States of America
State/province [14] 0 0
Virginia
Country [15] 0 0
Belgium
State/province [15] 0 0
Bruxelles
Country [16] 0 0
Belgium
State/province [16] 0 0
Edegem
Country [17] 0 0
Belgium
State/province [17] 0 0
Gent
Country [18] 0 0
Belgium
State/province [18] 0 0
Leuven
Country [19] 0 0
Germany
State/province [19] 0 0
Heidelberg
Country [20] 0 0
Germany
State/province [20] 0 0
Marburg
Country [21] 0 0
Hungary
State/province [21] 0 0
Budapest
Country [22] 0 0
Hungary
State/province [22] 0 0
Debrecen
Country [23] 0 0
Hungary
State/province [23] 0 0
Pecs
Country [24] 0 0
Hungary
State/province [24] 0 0
Szeged
Country [25] 0 0
Mexico
State/province [25] 0 0
Distrito Federal
Country [26] 0 0
Mexico
State/province [26] 0 0
Aguascalientes
Country [27] 0 0
Poland
State/province [27] 0 0
Gdansk
Country [28] 0 0
Poland
State/province [28] 0 0
Gorzow Wielkopolski
Country [29] 0 0
Poland
State/province [29] 0 0
Lodz
Country [30] 0 0
Poland
State/province [30] 0 0
Warszawa
Country [31] 0 0
Russian Federation
State/province [31] 0 0
Moscow
Country [32] 0 0
Russian Federation
State/province [32] 0 0
Saint Petersburg
Country [33] 0 0
Russian Federation
State/province [33] 0 0
Samara
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Slovakia
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Banska Bystrica
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Slovakia
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Bratislava
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Slovakia
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Kosice
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Spain
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Cataluña
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Spain
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Cataluña
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Spain
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Comunidad Valenciana
Country [40] 0 0
Spain
State/province [40] 0 0
PaÃ-s Vasco
Country [41] 0 0
Spain
State/province [41] 0 0
País Vasco
Country [42] 0 0
Spain
State/province [42] 0 0
Madrid

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Amgen
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
MD
Address 0 0
Amgen
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.