Skip to main content
OpenTrials
Completed

NCT Number: NCT05126784

AVT03 With Prolia in Healthy Male Subjects

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

28 year–55 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Nucleus Network, Herston, Australia

Loading trial locations.

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male subjects who are 28 to 55 years old, inclusive
  • Have a body weight of 50.0 to 90.0 kg (inclusive) and body mass index (BMI) of 17.0 to 32.0 kg/m2 (inclusive)at Screening and Day -1
  • Medical history without evidence of a clinically significant disorder, condition, or disease that, in the opinion of the Investigator, would pose a risk to subject safety

Exclusion criteria

  • Any evidence of clinically relevant pathology, especially prior diagnosis of bone disease, or any uncontrolled condition that will affect bone metabolism (such as, but not limited to osteoporosis, osteogenesis imperfecta, hyperparathyroidism, hyperthyroidism, hypothyroidism, osteomalacia, rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, current flare-up of osteoarthritis and/or gout, active malignancy, renal disease, Paget's disease of the bone, recent bone fracture [within 6 months], and malabsorption syndrome)
  • Have osteonecrosis of the jaw (ONJ) or risk factors for ONJ such as invasive dental procedures (eg, tooth extraction, dental implants, oral surgery) within 6 months prior to Day 1 or intend to undergo such procedures during the study period, poor oral hygiene, periodontal, and/or pre existing dental disease
  • Have bone fractures within 6 months prior to Day -1.
  • Have a history of immunodeficiency
  • Those with skin allergies, or are susceptible to autoinflammatory skin disorders, or prone to the development of allergic skin inflammation
  • Abnormal serum calcium: current hypocalcemia or hypercalcemia at Screening. Serum calcium levels must be within reference ranges.
  • Known vitamin D deficiency

Treatment and study plan

AVT03

Biological

AVT03 (biosimilar to denosumab) will be given as single subcutaneous injection

Other names: AVT03, Biosimilar Denosumab

Prolia

Biological

Prolia (denosumab) will be given as single subcutaneous injection

Other names: Denosumab

Primary outcomes

  1. Area under the serum concentration-time curve (AUC0-last) from day 0 to day 252

    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

  2. Area under the serum concentration-time curve (AUC0-inf) from day 0 to day 252

    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.

  3. Maximum serum concentration Cmax from day 0 to day 252

    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.

Secondary outcomes

  1. PD_AUCE0 for CTX-1 (% inhibition)

    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

  2. PK area under the concentration-time curve (AUC0-24) from Day 0 to Day 252

    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

  3. Safety incidence, nature and severity of adverse events

    Time frame: Screening to Day 252 (week 36)

  4. Immunogenicity presence and titers of ADAs and presence of nAbs against 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 antidrug-antibodies against of AVT03 and Prolia

Sponsors and collaborators

Lead sponsor

Alvotech Swiss AG

Industry

Registry information

Official study title

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

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Nov 19, 2021
Registry last updated
May 29, 2024

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.

Published trials that share one or more normalized conditions with this study.