drugset / Trial / NCT05238701

A Dose-escalation Study to Evaluate the Safety, Tolerability and Pharmacokinetic of LPM3770164 in Healthy Subjects

NCT05238701 ↗

Phase 1 Completed 104 enrolled Luye Pharma Group Ltd.
RandomizedSequentialQuadruple-blindTreatment

Summary

This is a single-center, randomized, double-blinded, placebo-controlled, dose escalation trial to evaluate the safety, tolerability and pharmacokinetic of LPM3770164 sustained-release tablets orally administered in healthy subjects under fasting state, providing the rationale information for subsequent clinical trials.

Timeline

Start
2022-02-25
Primary completion
2023-11-04
Completion
2023-11-04

Drugs

EvaluationDrugModalityDoseRoute
Subject LPM3770164 Unknown — Oral