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Safety, Pharmacokinetics, and Clinical Effects of Cinacalcet (AMG 073) in Primary Hyperparathyroidism

Primary Purpose

Primary Hyperparathyroidism

Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Cinacalcet
Placebo
Sponsored by
Amgen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Primary Hyperparathyroidism

Eligibility Criteria

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

Inclusion Criteria:

  1. Males and females ≥ 18 years of age at screening. In Part 1, females must be postmenopausal (at least 12 months since last menstrual period) or surgically sterile.

    In Part 2, all qualified females replacing a Part 1 subject (i.e., naïve subjects), regardless of reproductive status, may participate if, in the opinion of the principal investigator, an appropriate effective contraceptive method is used throughout the study. All females must have a negative serum pregnancy test within 28 days prior to Baseline (Parts 1 and 2).

  2. Men and women participating in this study must agree to use, in the opinion of the principal investigator, highly effective contraceptive measures throughout the study. All females who are pregnant or breast-feeding are excluded. All subjects must notify the principal investigator if they or their partner suspects a pregnancy.
  3. Diagnosis of primary HPT. A plasma intact PTH concentration ≥ 45 pg/mL on at least two occasions at least 1 week apart during the 12 months prior to baseline (at least one of these determinations should be made during screening), and a corrected total serum calcium concentration (for each 1 g/dL decrease in albumin level below 4.0 g/dL, the calcium value should be increased by 0.8 mg/dL) greater than the upper limit of normal, but no greater than 12.5 mg/dL.
  4. Acceptable renal function, with an estimated creatinine clearance > 50 ml/min as determined by the Cockroft and Gault equation.
  5. Acceptable hepatic function, defined as serum aspartate aminotransferase (AST), alanine aminotransferase (ALT), and total bilirubin < 2 times the upper limit of normal.
  6. Fasting (8 hours) serum glucose ≤ 130 mg/dL and hemoglobin Alc within the central laboratory's normal range.
  7. Hematology panel, serum clinical chemistry and urinalysis results within normal ranges
  8. Chest x-ray without evidence of active, infectious, inflammatory or malignant process.

Exclusion Criteria:

  1. Any unstable medical condition, defined as having been hospitalized within 28 at prior to baseline, or otherwise unstable in the judgement of the investigator.
  2. Received within 21 day prior to baseline, therapy with systemic glucocorticoids, lithium, tricyclic antidepressants, thioridazine, haloperidol, flecainide, or other drugs with a narrow therapeutic index that are primarily metabolized by hepatic cytochrome P450 CYP 2D6, drugs that affect renal tubular calcium handling (e.g. thiazide or loop diuretics), and drugs that affect bone metabolism (e.g. calcitonin, selective estrogen receptor modulators [SERMs])
  3. Received, within 90 days prior to Baseline, chronic therapy with bisphosphonates or fluoride.
  4. Known alcohol abuse, or use of illicit drugs, within 12 months prior to Baseline
  5. Experienced a myocardial infarction (MI) within 6 months prior to Baseline
  6. A ventricular rhythm disturbance requiring current treatment
  7. Received investigational drugs within 28 days prior to Baseline
  8. A history of seizures within 12 months prior to Baseline
  9. A history (within 5 years) of malignancy of any type, other than nonmelanomatous skin cancers or in situ cervical cancer
  10. A gastrointestinal disorder that may be associated with impaired absorption of orally administered medications
  11. A Body Mass Index (BMI) < 15 or > 40, obtained during screening
  12. An inability to swallow capsules
  13. Sarcoidosis, tuberculosis, or other diseases known to cause hypercalcemia
  14. Fasting spot urine calcium/creatinine ratio (mg) < 0.05
  15. A psychiatric disorder that would interfere with understanding and giving informed consent or compliance with protocol requirements
  16. Any other condition that might reduce the chance of obtaining data (eg, known poor compliance) required by the protocol or that might compromise the ability to give truly informed consent.
  17. For Part 2, a subject from Part 1 who discontinued treatment early

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm Type

    Placebo Comparator

    Experimental

    Experimental

    Experimental

    Arm Label

    Placebo

    Cinacalcet 50 mg QD

    Cinacalcet 75 mg QD

    Cinacelcet 100 mg QD

    Arm Description

    In Part 1 participants received placebo capsules orally once a day for 6 weeks. In Part 2 participants received placebo capsules twice a day for 15 days.

    In Part 1 participants received 50 mg cinacalcet capsules orally once a day (QD) for 6 weeks. In Part 2 participants received 30 mg cinacalcet capsules twice a day for 15 days.

    In Part 1 participants received 75 mg cinacalcet capsules orally once a day (QD) for 6 weeks. In Part 2 participants received 40 mg cinacalcet capsules twice a day for 15 days.

    In Part 1 participants received 100 mg cinacalcet capsules orally once a day (QD) for 6 weeks. In Part 2 participants received 50 mg cinacalcet capsules twice a day for 15 days.

    Outcomes

    Primary Outcome Measures

    Number of Participants with Adverse Events in Part 1 and Part 2

    Secondary Outcome Measures

    Percent Change from Baseline in Serum Calcium Concentration
    Area Under the Serum Calcium Concentration-time Curve from 0 to 24 Hours After Dosing (AUC0-24) in Part 1
    Area Under the Serum Calcium Concentration-time Curve from 0 to 12 Hours After Dosing (AUC0-12) in Part 2
    Minimum Serum Calcium Concentration in Part 1
    Minimum Serum Calcium Concentration in Part 2
    Cumulative Time When Serum Calcium was Below Baseline During the 24-hour Dosing Interval in Part 1
    Cumulative Time When Serum Calcium was Below Baseline During the 12-hour Dosing Interval in Part 2
    Cumulative Time Over the Day When Serum Calcium was ≤ 10.3 mg/dL In Part 1
    Cumulative Time Over the Day When Serum Calcium was ≤ 10.3 mg/dL In Part 2
    Percent Change from Baseline in Plasma Intact parathyroid Hormone (iPTH) Concentration
    Area Under the Plasma iPTH Concentration-time Curve from 0 to 24 Hours After Dosing (AUC0-24) in Part 1
    Area Under the Plasma iPTH Concentration-time Curve from 0 to 12 Hours After Dosing (AUC0-12) in Part 2
    Minimum iPTH Concentration in Part 1
    Minimum iPTH Concentration in Part 2
    Time of Minimum iPTH Concentration in Part 1
    Time of Minimum iPTH Concentration in Part 2
    Cumulative Time When iPTH was Below Baseline During the 24-hour Dosing Interval in Part 1
    Cumulative Time When iPTH was Below Baseline During the 12-hour Dosing Interval in Part 2
    Cumulative Time iPTH was Below 45 pg/mL in Part 1
    Cumulative Time iPTH was Below 45 pg/mL in Part 2
    Percent Change from Baseline in Serum Calcitonin Concentration
    Percentage of Participants with Serum Calcitonin Concentration Less than 10 pg/mL
    Percent Change from Baseline in Bone-specific Alkaline Phosphatase (BALP) Concentration
    Percentage of Participants with BALP Concentration Within Normal Range
    Normal range of BALP is 2.9 to 20.1 ng/mL for men 20 to 79 years of age and and 3.7 to 20.9 ng/mL for women 20 to 79 years of age.
    Percent Change from Baseline in Serum N-telopeptide (NTx) Concentration
    Percentage of Participants with Serum NTx Concentration Within Normal Range
    Normal range of serum NTx is 5.4 to 24.2 nmoL bone collagen equivalents (BCE)/L for men, 6.2 to 19.0 nmoL BCE/L for premenopausal women, and 5.3 to 35.8 nmol BCE/L for postmenopausal women (≥ 55 years).
    Percent Change from Baseline in Urinary NTx Concentration
    Percentage of Participants with Urinary NTx Concentration Within Normal Range
    Normal range of urinary NTx is is 0.0 to 85.0 nmoL BCE/mmoL creatinine for men, 5.0 to 65.0 nmoL BCE/mmoL creatinine for premenopausal women, and 0.0 to 130.0 nmoL BCE/mmoL creatinine for postmenopausal women [≥ 55 years).
    Percent Change from Baseline in Urinary Calcium/Creatinine Ratio
    Percent Change from Baseline in Urinary Calcium Concentration
    Percentage of Participants with Urinary Calcium Concentration Within Normal Range
    Normal range of urinary calcium is 50 to 300 mg/24 hours.
    Percent Change from Baseline in 1,25-Dihydroxy Vitamin D
    Percentage of Participants with 1,25-Dihydroxy Vitamin D Concentration in the Normal Range
    The normal range for 1,25-dihydroxy vitamin D3 is 16.0 to 65.0 pg/mL.
    Percent Change from Baseline in Urinary and Serum Phosphorus Concentrations

    Full Information

    First Posted
    December 11, 2018
    Last Updated
    December 11, 2018
    Sponsor
    Amgen
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03774771
    Brief Title
    Safety, Pharmacokinetics, and Clinical Effects of Cinacalcet (AMG 073) in Primary Hyperparathyroidism
    Official Title
    A Randomized, Double-Blind, Placebo-Controlled, Multicenter, 6-week Dose-Ranging Study to Assess the Safety, Pharmacokinetics, and Clinical Effects of an Oral Calcimimetic Agent (AMG 073) in Primary Hyperparathyroidism
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    September 29, 1998 (Actual)
    Primary Completion Date
    December 13, 1999 (Actual)
    Study Completion Date
    December 13, 1999 (Actual)

    3. Sponsor/Collaborators

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

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    Yes
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The primary objective was to assess the safety and tolerability of cinacalcet in adults with primary hyperparathyroidism (HPT) when administered as a single oral once daily doses for 6 consecutive weeks and twice daily for 15 consecutive days.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Primary Hyperparathyroidism

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Sequential Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    48 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Placebo
    Arm Type
    Placebo Comparator
    Arm Description
    In Part 1 participants received placebo capsules orally once a day for 6 weeks. In Part 2 participants received placebo capsules twice a day for 15 days.
    Arm Title
    Cinacalcet 50 mg QD
    Arm Type
    Experimental
    Arm Description
    In Part 1 participants received 50 mg cinacalcet capsules orally once a day (QD) for 6 weeks. In Part 2 participants received 30 mg cinacalcet capsules twice a day for 15 days.
    Arm Title
    Cinacalcet 75 mg QD
    Arm Type
    Experimental
    Arm Description
    In Part 1 participants received 75 mg cinacalcet capsules orally once a day (QD) for 6 weeks. In Part 2 participants received 40 mg cinacalcet capsules twice a day for 15 days.
    Arm Title
    Cinacelcet 100 mg QD
    Arm Type
    Experimental
    Arm Description
    In Part 1 participants received 100 mg cinacalcet capsules orally once a day (QD) for 6 weeks. In Part 2 participants received 50 mg cinacalcet capsules twice a day for 15 days.
    Intervention Type
    Drug
    Intervention Name(s)
    Cinacalcet
    Other Intervention Name(s)
    AMG 073, Sensipar®, Mimpara®
    Intervention Description
    Capsule for oral administration
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo
    Intervention Description
    Capsules for oral administration
    Primary Outcome Measure Information:
    Title
    Number of Participants with Adverse Events in Part 1 and Part 2
    Time Frame
    6 weeks in Part 1 and 15 days in Part 2
    Secondary Outcome Measure Information:
    Title
    Percent Change from Baseline in Serum Calcium Concentration
    Time Frame
    Baseline and days 8, 15, 16, 29, 43, and 50 in Part 1 and days 1, 8, 15, and 22 in Part 2.
    Title
    Area Under the Serum Calcium Concentration-time Curve from 0 to 24 Hours After Dosing (AUC0-24) in Part 1
    Time Frame
    Days 1, 8, and 43: Predose, 1, 2, 4, 8, 12, and 24 hours post dose
    Title
    Area Under the Serum Calcium Concentration-time Curve from 0 to 12 Hours After Dosing (AUC0-12) in Part 2
    Time Frame
    Days 1 and 15: Predose, 1, 2, 4, 8, 12, 13, 14, 16, 20, and 24 hours postdose
    Title
    Minimum Serum Calcium Concentration in Part 1
    Time Frame
    Days 1, 8, and 43: Predose, 1, 2, 4, 8, 12, and 24 hours postdose
    Title
    Minimum Serum Calcium Concentration in Part 2
    Time Frame
    Days 1 and 15: Predose, 1, 2, 4, 8, 12, 13, 14, 16, 20, and 24 hours postdose
    Title
    Cumulative Time When Serum Calcium was Below Baseline During the 24-hour Dosing Interval in Part 1
    Time Frame
    Days 1, 8, and 43: Predose, 1, 2, 4, 8, 12, and 24 hours post dose
    Title
    Cumulative Time When Serum Calcium was Below Baseline During the 12-hour Dosing Interval in Part 2
    Time Frame
    Days 1 and 15: Predose, 1, 2, 4, 8, 12, 13, 14, 16, 20, and 24 hours postdose
    Title
    Cumulative Time Over the Day When Serum Calcium was ≤ 10.3 mg/dL In Part 1
    Time Frame
    Days 1, 8, and 43: Predose, 1, 2, 4, 8, 12, and 24 hours post dose
    Title
    Cumulative Time Over the Day When Serum Calcium was ≤ 10.3 mg/dL In Part 2
    Time Frame
    Days 1 and 15: Predose, 1, 2, 4, 8, 12, 13, 14, 16, 20, and 24 hours postdose
    Title
    Percent Change from Baseline in Plasma Intact parathyroid Hormone (iPTH) Concentration
    Time Frame
    Baseline and days 8, 15, 16, 29, 43, and 50 in Part 1 and days 1, 8, 15, and 22 in Part 2.
    Title
    Area Under the Plasma iPTH Concentration-time Curve from 0 to 24 Hours After Dosing (AUC0-24) in Part 1
    Time Frame
    Days 1, 8, and 43: Predose, 1, 2, 4, 8, 12, and 24 hours post dose
    Title
    Area Under the Plasma iPTH Concentration-time Curve from 0 to 12 Hours After Dosing (AUC0-12) in Part 2
    Time Frame
    Days 1 and 15: Predose, 1, 2, 4, 8, 12, 13, 14, 16, 20, and 24 hours postdose
    Title
    Minimum iPTH Concentration in Part 1
    Time Frame
    Days 1, 8, and 43: Predose, 1, 2, 4, 8, 12, and 24 hours postdose
    Title
    Minimum iPTH Concentration in Part 2
    Time Frame
    Days 1 and 15: Predose, 1, 2, 4, 8, 12, 13, 14, 16, 20, and 24 hours postdose
    Title
    Time of Minimum iPTH Concentration in Part 1
    Time Frame
    Days 1, 8, and 43: Predose, 1, 2, 4, 8, 12, and 24 hours postdose
    Title
    Time of Minimum iPTH Concentration in Part 2
    Time Frame
    Days 1 and 15: Predose, 1, 2, 4, 8, 12, 13, 14, 16, 20, and 24 hours postdose
    Title
    Cumulative Time When iPTH was Below Baseline During the 24-hour Dosing Interval in Part 1
    Time Frame
    Days 1, 8, and 43: Predose, 1, 2, 4, 8, 12, and 24 hours post dose
    Title
    Cumulative Time When iPTH was Below Baseline During the 12-hour Dosing Interval in Part 2
    Time Frame
    Days 1 and 15: Predose, 1, 2, 4, 8, 12, 13, 14, 16, 20, and 24 hours postdose
    Title
    Cumulative Time iPTH was Below 45 pg/mL in Part 1
    Time Frame
    Days 1, 8, and 43: Predose, 1, 2, 4, 8, 12, and 24 hours post dose
    Title
    Cumulative Time iPTH was Below 45 pg/mL in Part 2
    Time Frame
    Days 1 and 15: Predose, 1, 2, 4, 8, 12, 13, 14, 16, 20, and 24 hours postdose
    Title
    Percent Change from Baseline in Serum Calcitonin Concentration
    Time Frame
    Baseline and days 8, 15, and 43 in Part 1
    Title
    Percentage of Participants with Serum Calcitonin Concentration Less than 10 pg/mL
    Time Frame
    Baseline and days 8, 15 and 43 in Part 1
    Title
    Percent Change from Baseline in Bone-specific Alkaline Phosphatase (BALP) Concentration
    Time Frame
    Baseline and days 15 and 43 in Part 1 and days 1, 8, and 15 in Part 2
    Title
    Percentage of Participants with BALP Concentration Within Normal Range
    Description
    Normal range of BALP is 2.9 to 20.1 ng/mL for men 20 to 79 years of age and and 3.7 to 20.9 ng/mL for women 20 to 79 years of age.
    Time Frame
    Baseline and days 15 and 43 in Part 1 and days 1, 8, and 15 in Part 2
    Title
    Percent Change from Baseline in Serum N-telopeptide (NTx) Concentration
    Time Frame
    Baseline and days 8 and 15 in Part 1
    Title
    Percentage of Participants with Serum NTx Concentration Within Normal Range
    Description
    Normal range of serum NTx is 5.4 to 24.2 nmoL bone collagen equivalents (BCE)/L for men, 6.2 to 19.0 nmoL BCE/L for premenopausal women, and 5.3 to 35.8 nmol BCE/L for postmenopausal women (≥ 55 years).
    Time Frame
    Baseline and days 8 and 15 in Part 1
    Title
    Percent Change from Baseline in Urinary NTx Concentration
    Time Frame
    Baseline and days 15 and 43 in Part 1 and days 1, 8, and 15 in Part 2
    Title
    Percentage of Participants with Urinary NTx Concentration Within Normal Range
    Description
    Normal range of urinary NTx is is 0.0 to 85.0 nmoL BCE/mmoL creatinine for men, 5.0 to 65.0 nmoL BCE/mmoL creatinine for premenopausal women, and 0.0 to 130.0 nmoL BCE/mmoL creatinine for postmenopausal women [≥ 55 years).
    Time Frame
    Baseline and days 15 and 43 in Part 1 and days 1, 8, and 15 in Part 2
    Title
    Percent Change from Baseline in Urinary Calcium/Creatinine Ratio
    Time Frame
    Baseline and days 8 and 15 in Part 1
    Title
    Percent Change from Baseline in Urinary Calcium Concentration
    Time Frame
    Baseline and days 15 and 43 in Part 1 and days 1, 8, and 15 in Part 2
    Title
    Percentage of Participants with Urinary Calcium Concentration Within Normal Range
    Description
    Normal range of urinary calcium is 50 to 300 mg/24 hours.
    Time Frame
    Baseline and days 15 and 43 in Part 1 and days 1, 8, and 15 in Part 2
    Title
    Percent Change from Baseline in 1,25-Dihydroxy Vitamin D
    Time Frame
    Baseline and days 8 and 43 in Part 1 and days 1 and 15 in part 2
    Title
    Percentage of Participants with 1,25-Dihydroxy Vitamin D Concentration in the Normal Range
    Description
    The normal range for 1,25-dihydroxy vitamin D3 is 16.0 to 65.0 pg/mL.
    Time Frame
    Baseline and days 8 and 43 in Part 1 and days 1 and 15 in part 2
    Title
    Percent Change from Baseline in Urinary and Serum Phosphorus Concentrations
    Time Frame
    Baseline and days 8, 15, and 22 in Part 2

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Males and females ≥ 18 years of age at screening. In Part 1, females must be postmenopausal (at least 12 months since last menstrual period) or surgically sterile. In Part 2, all qualified females replacing a Part 1 subject (i.e., naïve subjects), regardless of reproductive status, may participate if, in the opinion of the principal investigator, an appropriate effective contraceptive method is used throughout the study. All females must have a negative serum pregnancy test within 28 days prior to Baseline (Parts 1 and 2). Men and women participating in this study must agree to use, in the opinion of the principal investigator, highly effective contraceptive measures throughout the study. All females who are pregnant or breast-feeding are excluded. All subjects must notify the principal investigator if they or their partner suspects a pregnancy. Diagnosis of primary HPT. A plasma intact PTH concentration ≥ 45 pg/mL on at least two occasions at least 1 week apart during the 12 months prior to baseline (at least one of these determinations should be made during screening), and a corrected total serum calcium concentration (for each 1 g/dL decrease in albumin level below 4.0 g/dL, the calcium value should be increased by 0.8 mg/dL) greater than the upper limit of normal, but no greater than 12.5 mg/dL. Acceptable renal function, with an estimated creatinine clearance > 50 ml/min as determined by the Cockroft and Gault equation. Acceptable hepatic function, defined as serum aspartate aminotransferase (AST), alanine aminotransferase (ALT), and total bilirubin < 2 times the upper limit of normal. Fasting (8 hours) serum glucose ≤ 130 mg/dL and hemoglobin Alc within the central laboratory's normal range. Hematology panel, serum clinical chemistry and urinalysis results within normal ranges Chest x-ray without evidence of active, infectious, inflammatory or malignant process. Exclusion Criteria: Any unstable medical condition, defined as having been hospitalized within 28 at prior to baseline, or otherwise unstable in the judgement of the investigator. Received within 21 day prior to baseline, therapy with systemic glucocorticoids, lithium, tricyclic antidepressants, thioridazine, haloperidol, flecainide, or other drugs with a narrow therapeutic index that are primarily metabolized by hepatic cytochrome P450 CYP 2D6, drugs that affect renal tubular calcium handling (e.g. thiazide or loop diuretics), and drugs that affect bone metabolism (e.g. calcitonin, selective estrogen receptor modulators [SERMs]) Received, within 90 days prior to Baseline, chronic therapy with bisphosphonates or fluoride. Known alcohol abuse, or use of illicit drugs, within 12 months prior to Baseline Experienced a myocardial infarction (MI) within 6 months prior to Baseline A ventricular rhythm disturbance requiring current treatment Received investigational drugs within 28 days prior to Baseline A history of seizures within 12 months prior to Baseline A history (within 5 years) of malignancy of any type, other than nonmelanomatous skin cancers or in situ cervical cancer A gastrointestinal disorder that may be associated with impaired absorption of orally administered medications A Body Mass Index (BMI) < 15 or > 40, obtained during screening An inability to swallow capsules Sarcoidosis, tuberculosis, or other diseases known to cause hypercalcemia Fasting spot urine calcium/creatinine ratio (mg) < 0.05 A psychiatric disorder that would interfere with understanding and giving informed consent or compliance with protocol requirements Any other condition that might reduce the chance of obtaining data (eg, known poor compliance) required by the protocol or that might compromise the ability to give truly informed consent. For Part 2, a subject from Part 1 who discontinued treatment early

    12. IPD Sharing Statement

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    Safety, Pharmacokinetics, and Clinical Effects of Cinacalcet (AMG 073) in Primary Hyperparathyroidism

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