Condition: Autoimmune · Sponsor: Janux Therapeutics
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.
This description comes directly from the study's public registry record.
Janux Therapeutics · 858-206-8471 · ARMV-011-001_ct.gov@januxrx.com
Always discuss trial participation with your own doctor first.
| CMAX | Adelaide, South Australia, Australia | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07291323