Overview

A Trial to Compare the Pharmacokinetics of Tralokinumab in Healthy Subjects

Status:
Active, not recruiting
Trial end date:
2021-12-28
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this trial is to compare the pharmacokinetics (PK), safety, tolerability and immunogenicity of a single dose of 300 mg tralokinumab administered as a 1 × X mL subcutaneous (SC) injection with Device A and 2 × Y mL consecutive SC injections with Device B.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
LEO Pharma
Treatments:
Antibodies, Monoclonal
Criteria
Inclusion Criteria:

- Healthy male or female aged 18 to 55 years (both included) at the time of Screening.

- Female subjects of childbearing potential must use a highly effective form of birth
control throughout the trial and at least for 16 weeks after last administration of
the investigational medicinal product (IMP) and must have a negative serum pregnancy
test at Screening.

Exclusion Criteria:

- Systemic (non biologic) or topical treatment within 21 days prior to first dose
administration unless in the opinion of the Investigator the medication will not
interfere with the trial procedures or compromise safety.

- Active tuberculosis or history of incompletely treated tuberculosis based on medical
history or medical report.

- History of any known primary immunodeficiency disorder including a positive human
immunodeficiency virus (HIV) test at Screening, or the subject taking antiretroviral
medications as determined by medical history and/or subject's verbal report.

- History of a clinically significant infection (systemic infection or serious skin
infection requiring parenteral treatment) within 4 weeks prior to randomization.

- History of a helminth parasitic infection within 6 months prior to the date of
informed consent that has not been treated with or has failed to respond to standard
of care therapy.

- History of anaphylaxis or severe allergic reaction following any biologic therapy