Clinical Trial

Study of STLX-2012 in Healthy Volunteers

Not Yet Recruiting Phase 1
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Summary
The purpose of this research is to establish the safety, tolerability, pharmacokinetics, pharmacodynamics, and immunogenicity of a single IV dose of STLX-2012.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-11-14.
Trial Details
NCT Number NCT07231744
Lead Sponsor Stelexis BioSciences
Conditions Healthy Participants
Enrollment 32 participants
Start Date 2026-10
Primary Completion 2027-02 (estimated)
Study Completion 2027-02 (estimated)
Updated on ClinicalTrials.gov 2026-04-22