Romosozumab
DrugAdministered as three 70 mg/mL prefilled syringe injections
Other names: AMG 785, EVENITY™
NCT Number: NCT01833754
The purpose of this study is to evaluate the safety, tolerability, and immunogenicity profile of romosozumab after a single 210 mg subcutaneous dose in healthy participants and patients with stage 4 renal impairment (RI) or stage 5 RI requiring hemodialysis.
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Notify Me50 year and older
All sexes
Interventional
Phase 1
Research Site, Tempe, Arizona, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- ALL SUBJECTS :
Inclusion criteria
- SUBJECTS WITH RENAL IMPAIRMENT (GROUPS 1 AND 2):
Inclusion criteria
- HEALTHY SUBJECTS (GROUP 3):
Exclusion criteria
- ALL SUBJECTS:
Administered as three 70 mg/mL prefilled syringe injections
Other names: AMG 785, EVENITY™
Time frame: From the first dose of study drug up to day 85
A serious adverse event was defined as an adverse event (AE) that met at least 1 of the following serious criteria:
Time frame: Baseline and day 85
Two validated assays were used to detect the presence of anti-romosozumab antibodies. First, an electrochemiluminescent immunoassay was used to detect binding antibodies (screening assay) and confirm antibodies (confirmatory assay) capable of binding romosozumab. Second, a non-cell-based competitive binding bioassay was used to test positive binding antibody samples for neutralizing activity against romosozumab.
If a sample was positive for binding antibodies and demonstrated neutralizing activity at the same time point, the participant was defined as positive for neutralizing antibodies.
Time frame: Baseline, days 8, 15, 22, 29, 43, 57, and 85/end of study visit
Albumin-adjusted calcium was derived as:
Where serum albumin < 40 g/L then albumin-adjusted calcium = measured total calcium (mmol/L) + 0.02 * [40 - serum albumin (g/L)]; Where serum albumin ≥ 40 g/L then albumin-adjusted calcium = measured total calcium.
Time frame: Baseline, days 8, 15, 22, 29, 43, 57, and 85/end of study visit
Time frame: Pre-dose on day -1 and on days 2, 3, 4, 6, 8, 11, 15, 18, 22, 29, 36, 43, 57 and 85
Time frame: Pre-dose on day -1 and on days 2, 3, 4, 6, 8, 11, 15, 18, 22, 29, 36, 43, 57 and 85
Time frame: Pre-dose on day -1 and on days 2, 3, 4, 6, 8, 11, 15, 18, 22, 29, 36, 43, 57 and 85
Time frame: Pre-dose on day -1 and on days 2, 3, 4, 6, 8, 11, 15, 18, 22, 29, 36, 43, 57 and 85
Amgen
Industry
A Phase 1, Open-label, Single-dose Study of Romosozumab (AMG 785) Administered Subcutaneously to Healthy Subjects and Subjects With Stage 4 Renal Impairment or Stage 5 Renal Impairment Requiring Hemodialysis
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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