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Clinical Trials/NCT01825785
NCT01825785
Completed
Phase 1

A Randomized, Double-blind, Placebo-controlled, Ascending Multiple Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AMG 785 in Healthy Men and Postmenopausal Women With Low Bone Mass

Amgen0 sites48 target enrollmentNovember 14, 2007

Overview

Phase
Phase 1
Intervention
Placebo
Conditions
Postmenopausal
Sponsor
Amgen
Enrollment
48
Primary Endpoint
Number of Participants Who Developed Antibodies to Romosozumab
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The primary objective of this study was to assess the safety, tolerability, and immunogenicity potential of romosozumab following multiple subcutaneous (SC) administrations in healthy men and postmenopausal women with low bone mass.

Registry
clinicaltrials.gov
Start Date
November 14, 2007
End Date
December 2, 2008
Last Updated
2 years ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Sponsor
Amgen
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Healthy males and females between 45 to 80 years of age
  • Postmenopausal females
  • Low bone mineral density, defined by bone mineral density (BMD) T-scores between -1.0 and -2.5, inclusive, for the lumbar spine \[L1-L4\] or total evaluable vertebrae \[if fewer than L1-L4\] or total hip)
  • 25-hydroxyvitamin D ≥ 20 ng/mL
  • Weight ≤ 98 kg (216 lb) and/or height ≤ 196 cm (77 in)

Exclusion Criteria

  • Osteoporosis defined by bone mineral density (BMD) T-scores \< -2.5 for the lumbar spine (L1-L4) or total evaluable vertebrae (if fewer than L1-L4) or total hip
  • Diagnosed with any condition that would affect bone metabolism
  • Previous exposure to AMG 785

Arms & Interventions

Placebo

Participants were randomized to receive matching placebo administered by subcutaneous injection once every 2 weeks (Q2W) or once every 4 weeks (Q4W) for 3 months.

Intervention: Placebo

Romosozumab

Participants were randomized to receive romosozumab administered by subcutaneous injection at doses of 1 mg/kg Q2W, 2 mg/kg Q4W, 2 mg/kg Q2W, or 3 mg/kg Q4W for 3 months.

Intervention: Romosozumab

Outcomes

Primary Outcomes

Number of Participants Who Developed Antibodies to Romosozumab

Time Frame: Blood samples for detection of anti-romosozumab antibodies were collected at day 1 (predose) and days 29 (predose), 57 (predose), 85, 113, 141, and 169.

All samples were tested for binding anti-romsozumab antibodies using an immunoassay; all antibody-positive samples were further tested in a bioassay to determine if the antibodies were neutralizing. Development of antibodies to romosozumab is defined as participants with a negative result at baseline and a positive result at any time postbaseline.

Number of Participants With Adverse Events

Time Frame: 169 days

Serious adverse events were any events that were fatal, were life-threatening (placed the participant at immediate risk of death), required in-patient hospitalization or prolongation of existing hospitalization, resulted in persistent or significant disability/incapacity, were congenital anomalies or birth defects, or were other significant medical hazards. Relatedness to investigational product was assessed by the investigator by means of the question: "Is there a reasonable possibility that the event may have been caused by the investigational product?'

Secondary Outcomes

  • Percent Change From Baseline in Bone Mineral Density of the Total Spine(Baseline and days 29, 85, 127, and 169)
  • Percent Change From Baseline in Bone Mineral Density at the Femoral Hip(Baseline and days 29, 85, 127, and 169)
  • Percent Change From Baseline in Bone Mineral Density of the Whole Body(Baseline and days 29, 85, 127, and 169)
  • Percent Change From Baseline in Procollagen Type 1 N-terminal Propeptide (P1NP)(Baseline and days 2, 4, 6, 8, 15, 22, 29, 36, 43, 50 (Q2W only), 57, 58 (Q4W only), 60 (Q4W only), 62 (Q4W only), 64, 71, 72 (Q2W only), 74 (Q2W only), 76 (Q2W only), 78, 85, 99, 113, 127, 141, 155 and 169)
  • Area Under the Concentration-time Curve for the Dosing Interval (AUC0-tau) for Romosozumab(Q2W dose groups: First dose on days 1 (predose) to 15 (predose); Last dose on days 71 (predose) to 169. Q4W dose groups: First dose on days 1 (predose) to 29 (predose); Last dose on days 57 (predose) to 169.)
  • Accumulation Ratio (AR) for Romosozumab(Q2W dose groups: First dose on days 1 (predose) to 15 (predose); Last dose on days 71 (predose) to 169. Q4W dose groups: First dose on days 1 (predose) to 29 (predose); Last dose on days 57 (predose) to 169.)
  • Percent Change From Baseline in Osteocalcin(Baseline and days 2, 4, 6, 8, 15, 22, 29, 36, 43, 50 (Q2W only), 57, 58 (Q4W only), 60 (Q4W only), 62 (Q4W only), 64, 71, 72 (Q2W only), 74 (Q2W only), 76 (Q2W only), 78, 85, 99, 113, 127, 141, 155 and 169)
  • Percent Change From Baseline in Serum C-telopeptide (sCTX)(Baseline and days 2, 4, 6, 8, 15, 22, 29, 36, 43, 50 (Q2W only), 57, 58 (Q4W only), 60 (Q4W only), 62 (Q4W only), 64, 71, 72 (Q2W only), 74 (Q2W only), 76 (Q2W only), 78, 85, 99, 113, 127, 141, 155 and 169)
  • Percent Change From Baseline in Bone-specific Alkaline Phosphatase (BSAP)(Baseline and days 2, 4, 6, 8, 15, 22, 29, 36, 43, 50 (Q2W only), 57, 58 (Q4W only), 60 (Q4W only), 62 (Q4W only), 64, 71, 72 (Q2W only), 74 (Q2W only), 76 (Q2W only), 78, 85, 99, 113, 127, 141, 155 and 169)
  • Change From Baseline in Ionized Calcium(Baseline and day 169 (or earlier for participants who discontinued before day 169))
  • Time to Maximum Observed Concentration (Tmax) of Romosozumab(Q2W dose groups: First dose on days 1 (predose) to 15 (predose); Last dose on days 71 (predose) to 169. Q4W dose groups: First dose on days 1 (predose) to 29 (predose); Last dose on days 57 (predose) to 169.)
  • Maximum Observed Concentration (Cmax) of Romosozumab(Q2W dose groups: First dose on days 1 (predose) to 15 (predose); Last dose on days 71 (predose) to 169. Q4W dose groups: First dose on days 1 (predose) to 29 (predose); Last dose on days 57 (predose) to 169.)
  • Half-life Associated With the Terminal Phase of Elimination (T1/2) for Romosozumab(Q2W dose groups: days 71 (predose) to 169; Q24 dose groups: days 57 (predose) to 169.)
  • Percent Change From Baseline in Bone Mineral Density at the Total Hip(Baseline and days 29, 85, 127, and 169)
  • Percent Change From Baseline in Intact Parathyroid Hormone (iPTH)(Baseline and days 2, 4, 6, 8, 15, 22, 29, 36, 43, 50 (Q2W only), 57, 58 (Q4W only), 60 (Q4W only), 62 (Q4W only), 64, 71, 72 (Q2W only), 74 (Q2W only), 76 (Q2W only), 78, 85, 99, 113, 127, 141, 155 and 169)
  • Percent Change From Baseline in Bone Mineral Density at the Distal One-third Radius(Baseline and days 29, 85, 127, and 169)
  • Percent Change From Baseline in Bone Mineral Density at the Total Wrist(Baseline and days 29, 85, 127, and 169)
  • Percent Change From Baseline in Sclerostin(Baseline and days 15, 29, 43, 57, 71, 85, 99, 113, 127, 141, 155 and 169)

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