AVT03
BiologicalAVT03 (biosimilar to denosumab) will be given as single subcutaneous injection
Other names: AVT03, Biosimilar Denosumab
NCT Number: NCT05126784
This study has been designed as a randomized, double-blind, single-dose, parallel-group study in healthy adult male subjects 28 years to 55 years old. The study will assess the PK, PD, safety, tolerability and immunogenicity of AVT03 compared to Prolia when administered as a single SC dose.
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Notify Me28 year–55 year
Male
Interventional
Phase 1
Nucleus Network, Herston, Australia
The study will consist of a 4 week screening period, a 252 day (36 weeks) treatment and assessment period, and an End of Study (EOS) visit on week 36 on Day 252. Subjects will undertake a screening visit between Day -28 and Day -1 to determine their eligibility for the study. On Day 1, eligible subjects will be randomized and will receive a single dose of AVT03 or Prolia as subcutaneous injection.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
AVT03 (biosimilar to denosumab) will be given as single subcutaneous injection
Other names: AVT03, Biosimilar Denosumab
Prolia (denosumab) will be given as single subcutaneous injection
Other names: Denosumab
Time frame: Day 1(week 1) to Day 252 (week 36)
Venous blood samples will be collected for measurement of Area under serum concentration-time curve (AUC 0-t) AVT03 and Prolia
Time frame: Time Frame: Day 1(week 1) to Day 252 (week 36)]
Venous blood samples will be collected for measurement of CTX-1 serum biomarker for AVT03 and Prolia.
Time frame: Day 1(week 1) to Day 252 (week 36)
Venous blood samples will be collected for measurement of maximum serum concentration (Cmax) of AVT03 and Prolia.
Time frame: Day 1(week 1) to Day 252 (week 36)
Venous blood samples will be collected for measurement of serum concentration of AVT03 and Prolia
Time frame: Day 1(week 1) to Day 162 (week 24)]
Venous blood samples will be collected for measurement of serum concentration of AVT03 and Prolia
Time frame: Screening to Day 252 (week 36)
Time frame: Time Frame: Day 1(week 1) to Day 252 (week 36)
Venous blood samples will be collected for measurement of antidrug-antibodies against of AVT03 and Prolia
Alvotech Swiss AG
Industry
A Randomized, Double-blind, Single-dose, Parallel-group Design, 2 Arm Study Comparing the Pharmacokinetic, Pharmacodynamic, Safety, Tolerability, and Immunogenicity Profiles of AVT03 and Prolia® in Healthy Male Subjects
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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