drugset / Trial / NCT06995326

A Study of SGB-3383 in Healthy Subjects

NCT06995326 ↗

Phase 1 Not yet recruiting 37 enrolled Suzhou Sanegene Bio Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetic (PK), and pharmacodynamic (PD) effects of SGB-3383 in healthy subjects. The study will be designed as a single ascending dose (SAD) phase, utilizing a double-blind, placebo-controlled approach.

Timeline

Start
2025-06
Primary completion
2026-08
Completion
2027-01

Drugs

EvaluationDrugModalityDoseRoute
Subject SGB-3383 Unknown — Subcutaneous

Indications

No indication recorded.