drugset / Trial / NCT07231744

Study of STLX-2012 in Healthy Volunteers

NCT07231744 ↗

Phase 1 Not yet recruiting 32 enrolled Stelexis BioSciences
RandomizedParallel-groupDouble-blindBasic science

Summary

The purpose of this research is to establish the safety, tolerability, pharmacokinetics, pharmacodynamics, and immunogenicity of a single IV dose of STLX-2012.

Timeline

Start
2026-10
Primary completion
2027-02
Completion
2027-02

Drugs

EvaluationDrugModalityDoseRoute
Subject STLX-2012 Unknown — Intravenous

Indications

No indication recorded.