Garadacimab Safety, Pharmacokinetics, and Pharmacodynamics in Idiopathic Pulmonary Fibrosis

Purpose

This is a prospective, phase 2a, multicenter, randomized, double-blind, placebo-controlled, parallel-group study to assess the safety, pharmacokinetics (PK), and pharmacodynamics (PD) of garadacimab in subjects with idiopathic pulmonary fibrosis (IPF).

Condition

  • Idiopathic Pulmonary Fibrosis

Eligibility

Eligible Ages
Over 40 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Male or female patients ≥ 40 years of age - Documented diagnosis of IPF

Exclusion Criteria

  • History of clinically significant cardiovascular disease, including myocardial infarction, unstable ischemic heart disease, congestive heart failure, or angina during the 6 months before screening - Sinoatrial or atrioventricular block, uncontrolled hypertension - Active bleeding or current clinically significant coagulopathy

Study Design

Phase
Phase 2
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Garadacimab
Administered IV and SC
  • Drug: Garadacimab
    Participants received garadacimab intravenous (IV) loading dose followed by 3 subcutaneous (SC) doses.
    Other names:
    • Factor XIIa antagonist monoclonal antibody
    • CSL312
Placebo Comparator
Placebo
Administered IV and SC
  • Drug: Placebo
    Participants received a matching placebo IV loading dose, followed by 3 SC doses.

Recruiting Locations

More Details

NCT ID
NCT05130970
Status
Completed
Sponsor
CSL Behring