This first-in-human (FIH) study aims to characterize the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of JANX011 dosed subcutaneously (and potentially intravenously) in healthy adult volunteers (HVs) to gain insight into its therapeutic utility in patients with autoimmune diseases.
Protocol Amendment History
1 amendment
This ClinicalTrials.gov record has been amended once since 2025-12-05.
Status change: Not Yet Recruiting → Recruiting2026-04-20