drugset / Trial / NCT01588236

Effect of KYG0395 on Primary Dysmenorrhea

NCT01588236 ↗

Phase 2 Completed 280 enrolled Jiangsu Kanion Pharmaceutical Co., Ltd
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to further assess the efficacy, safety and dose-response of KYG0395 in the treatment of primary dysmenorrhea.

Timeline

Start
2012-05
Primary completion
2015-07
Completion
2015-07

Outcome

Mixed primary results

registry analysis (unspecified test); KYG0395 (High Dose Group) vs KYG0395 (Lower Dose Group) vs Placebo; p >0.05; Mixed Models Analysis NCT01588236 ↗

registry analysis (unspecified test); KYG0395 (High Dose Group) vs KYG0395 (Lower Dose Group) vs Placebo; p <0.01; Mixed Models Analysis NCT01588236 ↗

registry LEAST_SQUARES_MEAN KYG0395 (High Dose Group): -22.8 (Standard Error 2.93) unit of a scale NCT01588236 ↗

registry analysis (unspecified test); KYG0395 (High Dose Group) vs KYG0395 (Lower Dose Group) vs Placebo; p <0.05; Mixed Models Analysis NCT01588236 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject KYG0395 Unknown — —

Indications