drugset / Trial / NCT06563713

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of STSP-0902 in Healthy Subjects

NCT06563713 ↗

Phase 1 Completed 40 enrolled Staidson (Beijing) Biopharmaceuticals Co., Ltd
RandomizedSequentialQuadruple-blindTreatment

Summary

This is a Phase 1a, randomized, double-blind, placebo-controlled, single ascending dose (SAD) study to evaluate the safety, tolerability, pharmacokinetics (PK), and immunogenicity of STSP-0902.

Timeline

Start
2024-07-31
Primary completion
2025-02-24
Completion
2025-02-24

Drugs

EvaluationDrugModalityDoseRoute
Subject STSP-0902 Unknown — Subcutaneous

Indications