drugset / Trial / NCT04393675

Study to Investigate the Safety of LT5001 Drug Product for Uremic Pruritus in Hemodialysis Patients

NCT04393675 ↗

Phase 1/2 Terminated 18 enrolled Lumosa Therapeutics Co., Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

A Randomized, Double Blind, Placebo-Controlled study to assess the Safety, Local Tolerance, and Pharmacokinetics of LT5001 drug product in Hemodialysis Patients with Uremic Pruritus

Timeline

Start
2020-05-14
Primary completion
2022-09-15
Completion
2022-09-15

Outcome

Outcome not reported

Stopped: “Change in the clinical development plan”

Drugs

EvaluationDrugModalityDoseRoute
Comparator LT5001 Unknown 6 g —

Indications

No indication recorded.