drugset / Trial / NCT04208087

PK and Safety of SI-722 in IC/BPS

NCT04208087 ↗

Phase 1/2 Completed 33 enrolled Seikagaku Corporation
RandomizedSequentialQuadruple-blindTreatment

Summary

This study is designed randomized, double-blind, placebo-controlled trial in Interstitial Cystitis/Bladder Pain Syndrome patients.

Timeline

Start
2020-03-30
Primary completion
2021-01-12
Completion
2021-01-12

Outcome

Met primary endpoint

release “In tolerability evaluation, a primary objective of the study, the tolerability of SI-722 was confirmed, and the Company is currently considering the next-phase study.” seikagaku.co.jp ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject SI-722 Unknown — Other

Indications