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Completed

NCT Number: NCT04580654

A Study to Assess the Pharmacokinetics and Safety of CSL312 in Healthy Japanese and Caucasian Adults

This will be a 2- part, phase 1, open-label, single center, single ascending dose study to investigate the pharmacokinetics (PK), pharmacodynamics (PD), safety, and tolerability of subcutaneous (SC) and intravenous (IV) administration of CSL312 in healthy adult Japanese and Caucasian subjects.

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Key information

Conditions

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Anaheim Clinical Trials, LLC

Anaheim, California, 92801, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Healthy Caucasian and Japanese male or female subjects 18 to 55 years old (inclusive) that meet the following criteria at Screening:
  • Japanese subjects defined as being born in Japan, having not lived outside of Japan for more than 10 years, and having both parents and four grandparents who are of Japanese ancestry.
  • Caucasian subjects, defined as having both parents and four grandparents descended from and of the peoples of Europe, the Middle East, or North Africa, who are body weight-matched (± 15%) 1:1 with Japanese subjects.
  • Body weight in the range of ≥ 50 kg and ≤ 100 kg
  • Body mass index of ≥ 18 kg/m2 and ≤ 30 kg/m2

Exclusion criteria

  • Positive serology test for human immunodeficiency virus (HIV)-1 / 2 antibody, hepatitis B virus (HBV) surface antigen (HBsAg) or hepatitis C virus (HCV) antibody.
  • Received any live viral or bacterial vaccinations within 8 weeks of Screening or is expected to receive any live virus or bacterial vaccinations during the study.
  • Evidence of current active infection.
  • Known malignancy or a history of malignancy in the past 5 years .
  • Blood pressure or pulse rate measurements outside the normal range for the subject's age.
  • Female subject of childbearing potential or fertile male subject either not using or not willing to use an acceptable method of contraception
  • Pregnant, breastfeeding, or not willing to cease breastfeeding.
  • Donation or loss of more than 500 mL of blood within 3 months, or donated plasma within 7 days
  • History of clinically significant arterial or venous thrombosis, bleeding disorder, or any abnormal coagulation test result

Treatment and study plan

CSL312

Biological

Fully human immunoglobulin G4/lambda recombinant monoclonal antibody against Factor XIIa

Other names: Factor XIIa antagonist monoclonal antibody, garadacimab

Primary outcomes

  1. Maximum plasma concentration (Cmax) of CSL312 after subcutaneous dosing

    Time frame: Up to 85 days postdose

  2. Area under the curve (AUC) from time 0 extrapolated to infinity (AUC0-inf) of CSL312 after subcutaneous dosing

    Time frame: Up to 85 days postdose

Secondary outcomes

  1. Time to maximum concentration (Tmax) of CSL312 after subcutaneous dosing

    Time frame: Up to 85 days postdose

  2. Area under the concentration-time curve from time 0 to the last measurable concentration (AUC0-last) of CSL312 after subcutaneous dosing

    Time frame: Up to 85 days postdose

  3. Half-life (t1/2) of CSL312 after subcutaneous dosing

    Time frame: Up to 85 days postdose

  4. Apparent clearance (CL/F) of CSL312 after subcutaneous dosing

    Time frame: Up to 85 days postdose

  5. Apparent volume of distribution (Vz/F) of CSL312 after subcutaneous dosing

    Time frame: Up to 85 days postdose

  6. Cmax of CSL312 after intravenous dosing

    Time frame: Up to 85 days postdose

  7. Tmax of CSL312 after intravenous dosing

    Time frame: Up to 85 days postdose

  8. AUC0-last of CSL312 after intravenous dosing

    Time frame: Up to 85 days postdose

  9. AUC0-inf of CSL312 after intravenous dosing

    Time frame: Up to 85 days postdose

  10. t1/2 of CSL312 after intravenous dosing

    Time frame: Up to 85 days postdose

  11. Clearance (CL) of CSL312 after intravenous dosing

    Time frame: Up to 85 days postdose

  12. Volume of distribution (Vd) of CSL312 after intravenous dosing

    Time frame: Up to 85 days postdose

  13. Mean FXIIa-mediated kallikrein activity

    Time frame: Up to 85 days postdose

  14. Number of subjects experiencing adverse events (AEs)

    Time frame: Up to 85 days postdose

  15. Percentage of subjects experiencing AEs

    Time frame: Up to 85 days postdose

  16. Number of subjects experiencing serious adverse events (SAEs)

    Time frame: Up to 85 days postdose

  17. Percentage of subjects experiencing SAEs

    Time frame: Up to 85 days postdose

  18. Number of subjects experiencing adverse events of special interest (AESIs)

    Time frame: Up to 85 days postdose

  19. Percentage of subjects experiencing AESIs

    Time frame: Up to 85 days postdose

  20. Number of subjects experiencing Anti-CSL312 antibodies

    Time frame: Up to 85 days postdose

  21. Percentage of subjects experiencing Anti-CSL312 antibodies

    Time frame: Up to 85 days postdose

  22. Number of subjects with injection / infusion site reaction by severity

    Time frame: Up to 48 hours after start of infusion or injection

  23. Percentage of subjects with injection / infusion site reaction by severity

    Time frame: Up to 48 hours after start of infusion or injection

Sponsors and collaborators

Lead sponsor

CSL Behring

Industry

Registry information

Official study title

A 2-Part, Phase 1, Single Center, Open-label, Single Ascending Dose Study to Investigate the Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of Subcutaneous and Intravenous CSL312 in Healthy Adult Japanese and Caucasian Subjects

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Oct 8, 2020
Registry last updated
Oct 4, 2022

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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