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NCT05225857CompletedPhase 1

A First-in-Human Study Evaluating AGA2118 in Men and Postmenopausal Women

A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Single and Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, Absolute Bioavailability, Pharmacokinetics, and Pharmacodynamics of AGA2118 in Men and Postmenopausal Women

Source: ClinicalTrials.gov · Last updated 5 Feb 2024

Brief summary (registry, in English)

The primary objectives of the study are to assess the safety and tolerability of AGA2118 after single subcutaneous or intravenous administration in healthy men and postmenopausal women and to assess the safety and tolerability of AGA2118 after multiple subcutaneous administrations in men and postmenopausal women.

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
90 (actual)
First submitted
11 Jan 2022
Start date
28 Jun 2022
Primary completion date
13 Jan 2024
Lead sponsor
Angitia Biopharmaceuticals
Diseases
Osteoporosis
NCT number
NCT05225857

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 90
  • From 28 Jun 2022 to the primary completion date, 13 Jan 2024
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous exposure to AGA2118 (for MAD only).
  • Administration of the any medications that known to affect bone metabolism within 6 months of Day 1 unless otherwise specified (for SAD and MAD).

Other illness

  • Any condition that would affect bone metabolism or has a history of low energy fractures as documented in medical history (for MAD only).
  • Human immunodeficiency virus (HIV) infection (for SAD and MAD).
  • Active chronic hepatitis B (HBV) or hepatitis C (HCV) infection including hepatitis B surface antigen and hepatitis C antigen positive participants with or without abnormal liver enzymes (for SAD and MAD).

Lab values

  • Evidence of any of the following (for SAD and MAD):
    • creatinine ≥ 1.5 × ULN, or estimated glomerular filtration rate (eGFR) \< 60 mL/min/1.73 m\^2 using the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formula at screening
    • current hyper- or hypocalcemia, defined as albumin-adjusted serum calcium outside the normal range
    • known intolerance to calcium supplements
    • malignancy within the last 5 years, etc.

Other

  • A bone fracture within 6 months (for SAD only).

Who the study is looking for

  • Healthy men ≥ 30 and ≤ 65 years of age or postmenopausal women ≥ 45 and ≤ 65 years of age for SAD and MAD;
  • BMI ≥ 18.5 and ≤ 32 kg/m\^2 (for SAD and MAD).
  • Generally healthy (as assessed by the investigator).
  • Nonsmokers, or light smokers, defined as ≤ 3 cigarettes/day (or equivalent) (for SAD and MAD).
  • Able and willing to correctly and independently complete all study procedures and able to read, understand, and provide written informed consent after the nature of the study has been fully explained and must be willing to comply with all study requirements and procedures (for SAD and MAD).
  • A male who is sterile or agrees to the following during the Treatment Period and for at least 6 months after the final dose of investigational product
    • Refrain from donating fresh unwashed semen
    • Plus, either
  • Be abstinent from heterosexual intercourse as their preferred and usual lifestyle (abstinent on a long term and persistent basis) and agree to remain abstinent
    • OR
  • Must agree to use contraception as detailed below
    • Agree to use a male condom plus a female partner to use a highly effective method of contraception with a woman of childbearing potential who is not currently pregnant
    • Agree to use a male condom when engaging in any activity that allows for passage of ejaculate to another person

Age in the registry: 30 years to 65 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Q-Pharm Pty Ltd
Coordinator of this site? Confirm its status
BrisbaneAustraliaUnknown status
Nucleus Network Pty Ltd
Coordinator of this site? Confirm its status
MelbourneAustraliaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.