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NOT YET RECRUITING
NCT07231744
PHASE1

Study of STLX-2012 in Healthy Volunteers

Sponsor: Stelexis BioSciences

View on ClinicalTrials.gov

Summary

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

Official title: A Phase 1 Randomized, Double-Blind, Placebo-Controlled Study of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Ascending Doses of STLX-2012 in Healthy Volunteers

Key Details

Gender

All

Age Range

18 Years - 55 Years

Study Type

INTERVENTIONAL

Enrollment

32

Start Date

2026-02

Completion Date

2027-02

Last Updated

2025-11-17

Healthy Volunteers

Yes

Interventions

DRUG

STLX-2012

STLX-2012 IV

OTHER

Placebo

Placebo arm

Locations (1)

Nucleus Network Brisbane

Brisbane, Queensland, Australia