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Comparing the Extent to Which Romosozumab (AMG 785) is Made Available in the Body When Administered as a Single SC Injection or as 2 SC Injections

12 octobre 2026 mis à jour par: Amgen

A Phase 1, Open-label, Randomized, Parallel Group Study to Evaluate the Relative Bioavailability of Romosozumab (AMG 785) 210 mg Administered as a Single SC Injection or 2 SC Injections in Healthy Participants

The primary objective of this trial is to evaluate the relative bioavailability of romosozumab administered as a single 2.34 mL subcutaneous (SC) injection from a prefilled syringe (PFS) or 2 x 1.17 mL SC injections from PFS in healthy participants.

Aperçu de l'étude

Statut

Recrutement

Intervention / Traitement

Type d'étude

Interventionnel

Inscription (Estimé)

308

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

  • Nom: Amgen Call Center
  • Numéro de téléphone: 866-572-6436
  • E-mail: medinfo@amgen.com

Lieux d'étude

    • LDS
      • Leeds, LDS, Royaume-Uni, LS11 9EH
        • Recrutement
        • Fortrea Clinical Research Unit Limited - Leeds
    • Florida
      • Miami, Florida, États-Unis, 33143
        • Recrutement
        • QPS Miami

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 60 ans (Adulte)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  • Healthy adults, male or female, 18 to 60 years of age.
  • Able and willing to provide written informed consent before any study procedures.
  • Body weight between 45.0 kg and 95.0 kg (inclusive).
  • Women must not be able to become pregnant (for example, postmenopausal or permanently sterile, as defined by the protocol).
  • Men who can father a child must agree to use the required contraception during the study and for 3 months after the study drug dose.
  • Willing and able to take daily calcium (500 to 2,000 mg elemental calcium) and vitamin D (at least 400 IU) supplements from Day 1 through the end of the study.

Exclusion Criteria:

  • Any clinically significant medical condition or abnormal finding that, in the opinion of the study doctor, could make participation unsafe or interfere with the study or its results.
  • Clinically significant abnormalities on medical history, physical examination, vital signs, electrocardiogram (ECG), or laboratory tests, including suspected Gilbert syndrome.
  • History or current signs or symptoms of significant cardiovascular disease, including heart attack, heart failure, congenital heart disease, cardiomyopathy, valve disease, angina, coronary revascularization, stroke, transient ischemic attack, or peripheral revascularization.
  • Clinically significant abnormal heart rhythm or conduction disorder, including clinically significant ECG abnormalities.
  • QT interval corrected for heart rate (QTcF) greater than 450 milliseconds for men or greater than 470 milliseconds for women, or a history of long QT syndrome.
  • Second- or third-degree atrioventricular (AV) block.
  • Systolic blood pressure greater than 140 millimeters of mercury (mmHg) or less than 90 mmHg, diastolic blood pressure greater than 90 mmHg or less than 50 mmHg, or pulse rate greater than 100 beats per minute or less than 40 beats per minute at screening or check-in.
  • Deep vein thrombosis or pulmonary embolism within 3 months before screening.
  • History of osteoporosis, vertebral fracture, or a fragility fracture of the wrist, upper arm, hip, or pelvis after 50 years of age.
  • History of metabolic bone disease, including conditions such as Paget disease, osteomalacia, osteogenesis imperfecta, osteopetrosis, sclerosteosis, ankylosing spondylitis, rheumatoid arthritis, Cushing disease, hyperprolactinemia, or malabsorption syndrome.
  • History of osteonecrosis of the jaw.
  • Bone fracture within 6 months before screening.
  • Vitamin D level below 20 nanograms per milliliter (ng/mL) at screening (participants may be treated and retested before enrollment).
  • Current hyperparathyroidism or hypoparathyroidism.
  • Kidney function below study requirements (estimated glomerular filtration rate less than 60 mL/min/1.73 m^2).
  • Low or high blood calcium levels that do not meet study requirements.
  • Liver blood test results (alanine aminotransferase [ALT] or aspartate aminotransferase [AST]) above the normal range.
  • History of hyperthyroidism or hypothyroidism unless on stable treatment for at least 6 months with normal thyroid function tests.
  • History of hearing loss caused by excessive bone growth compressing the eighth cranial nerve.
  • Positive test for human immunodeficiency virus (HIV).
  • Active hepatitis B or hepatitis C infection.
  • Cancer within the past 5 years, except non-melanoma skin cancer or cervical or breast ductal carcinoma in situ.
  • History of solid organ or bone marrow transplantation.
  • History of allergy or hypersensitivity to romosozumab, its ingredients, other biologic medicines, or medicines derived from mammalian cells.
  • Previous use of medications affecting bone metabolism that are not allowed by the protocol, including:
  • Any intravenous or oral bisphosphonate.
  • Fluoride for osteoporosis within 24 months before screening.
  • Denosumab or cathepsin K inhibitors within 18 months before screening.
  • Parathyroid hormone or strontium within 12 months before screening.
  • Calcitonin, selective estrogen receptor modulators, or tibolone within 3 months before screening.
  • Systemic corticosteroids (5 mg or more prednisone equivalent daily for more than 10 days) within 3 months before screening.
  • Use of prescription or over-the-counter medications within 30 days or 5 half-lives (whichever is longer) before check-in, unless approved by the study doctor. Acetaminophen up to 2 g/day is permitted. Stable hormone replacement therapy is allowed if unchanged for at least 3 months before dosing and throughout the study.
  • Use of herbal medicines, vitamins (other than study-required calcium and vitamin D), or dietary supplements within 30 days before enrollment unless approved by the study doctor.
  • Currently participating in another clinical study, receiving another investigational treatment, or participation in another investigational drug or device study within the previous 90 days or 5 half-lives (whichever is longer).
  • Previous participation in this study or previous exposure to a sclerostin antibody.
  • History of alcohol abuse or regular alcohol intake greater than 14 units per week within the year before check-in.
  • Alcohol use within 48 hours before check-in or unwillingness to comply with study alcohol restrictions.
  • Positive alcohol test at check-in.
  • Positive drug screen for illicit drugs, including cannabis, at screening or check-in.
  • History of illicit drug use within 6 months before screening.
  • Unwilling to avoid illicit drug use, including cannabis, throughout the study.
  • Smoking more than 10 cigarettes per day or equivalent nicotine use within 1 month before check-in, or unwillingness to comply with study tobacco restrictions.
  • Consumption of foods or drinks containing poppy seeds within 7 days before check-in.
  • Positive pregnancy test at screening or check-in.
  • Pregnant, breastfeeding, or planning to breastfeed during the study or within 3 months after receiving the study drug.
  • Receipt of blood products within 2 months before check-in.
  • Blood donation within 3 months before screening, plasma donation within 2 weeks before screening, or platelet donation within 6 weeks before screening.
  • Poor veins that would make repeated blood sampling difficult.
  • Any other reason that, in the opinion of the study doctor, would make participation unsafe or inappropriate.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Science basique
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Romosozumab Test Arm

Participants will receive a single SC injection of romosozumab (test) administered using a PFS.

Romosozumab will be administered via SC injection using a PFS.

Autres noms:
  • AMG 785
  • Evenity®
Comparateur actif: Romosozumab Reference Arm

Participants will receive two SC injections of romosozumab (reference) administered using a PFS.

Romosozumab will be administered via SC injection using a PFS.

Autres noms:
  • AMG 785
  • Evenity®

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
Area Under the Concentration-time Curve From Time 0 Extrapolated to Infinity (AUCinf) of romosozumab
Délai: Up to Day 85
Up to Day 85
Area Under the Concentration-time Curve From Time 0 to Time of Last Quantifiable Concentration (AUClast) of romosozumab
Délai: Up to Day 85
Up to Day 85
Maximum Observed Serum Concentration (Cmax) of romosozumab
Délai: Up to Day 85
Up to Day 85

Mesures de résultats secondaires

Mesure des résultats
Délai
Number of Participants Who Experienced Treatment-Emergent Adverse Events and Serious Adverse Events
Délai: Up to Day 85
Up to Day 85
Number of Participants Who Developed Anti-romosozumab Antibodies
Délai: Up to Day 85
Up to Day 85

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Les enquêteurs

  • Directeur d'études: MD, Amgen

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

22 septembre 2026

Achèvement primaire (Estimé)

14 janvier 2027

Achèvement de l'étude (Estimé)

14 janvier 2027

Dates d'inscription aux études

Première soumission

4 septembre 2026

Première soumission répondant aux critères de contrôle qualité

4 septembre 2026

Première publication (Réel)

10 septembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

13 octobre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

12 octobre 2026

Dernière vérification

1 octobre 2026

Plus d'information

Termes liés à cette étude

Termes MeSH pertinents supplémentaires

Autres numéros d'identification d'étude

  • 20250008

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

OUI

Description du régime IPD

De-identified individual patient data for variables necessary to address the specific research question in an approved data sharing request.

Délai de partage IPD

Data sharing requests relating to this trial will be considered beginning 18 months after the trial has ended and either 1) the product and indication have been granted marketing authorization in both the US and Europe or 2) clinical development for the product and/or indication discontinues and the data will not be submitted to regulatory authorities. There is no end date for eligibility to submit a data sharing request for this trial.

Critères d'accès au partage IPD

Qualified researchers may submit a request containing the research objectives, the Amgen product(s) and Amgen trial/trials in scope, endpoints/outcomes of interest, statistical analysis plan, data requirements, publication plan, and qualifications of the researcher(s). In general, Amgen does not grant external requests for individual patient data for the purpose of re-evaluating safety and efficacy issues already addressed in the product labelling. Requests are reviewed by a committee of internal advisors. If not approved, a Data Sharing Independent Review Panel will arbitrate and make the final decision. Upon approval, information necessary to address the research question will be provided under the terms of a data sharing agreement. This may include anonymized individual patient data and/or available supporting documents, containing fragments of analysis code where provided in analysis specifications. Further details are available at the URL below.

Type d'informations de prise en charge du partage d'IPD

  • PROTOCOLE D'ÉTUDE
  • SÈVE
  • CIF
  • RSE

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Oui

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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