drugset / Trial / NCT06982352

Safety and Pharmacokinetics of LPX-TI641 in Atopic Dermatitis and Psoriasis

NCT06982352 ↗

Phase 1 Recruiting 48 enrolled LAPIX Therapeutics Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

The goal of this clinical trial is to study the drug LPX-TI641 in patients with atopic dermatitis and psoriasis. We will compare the safety and tolerability of LPX-TI641 to placebo ( a look-alike solution) that contains no drug. We will also evaluate the plasma pharmacokinetics of LPX-TI641. LPX-TI641 (or placebo) will be administered orally for 28 days.

Timeline

Start
2025-06-15
Primary completion
2026-01-15
Completion
2026-04-15

Drugs

EvaluationDrugModalityDoseRoute
Subject LPX-TI641 Small molecule 150 mg Oral

Indications