drugset / Trial / NCT07230652

A Phase 1 MAD Study to Evaluate the Safety and Tolerability of LY03020

NCT07230652 ↗

Phase 1 Recruiting 40 enrolled Luye Pharma Group Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a randomized, double-blind, placebo-controlled, ascending multiple oral dose study to assess the safety, tolerability, and pharmacokinetics of LY03020 in Chinese healthy adult subjects and/or subjects with stable schizophrenia.

Timeline

Start
2025-08-20
Primary completion
2025-12-31
Completion
2026-02-28

Drugs

EvaluationDrugModalityDoseRoute
Subject LY03020 Unknown — Oral