A Randomized, Placebo-controlled, Double-blind Study of KLH-2109 in Patients With Endometriosis (2)

Phase 2CompletedNCT01533532

Kissei Pharmaceutical Co., Ltd.100 enrolled

Overview

The purpose of this study is to evaluate the efficacy and safety of KLH-2109 in patients with endometriosis.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

100

Conditions

Endometriosis

Interventions

KLH-2109DRUG

placeboDRUG

Eligibility

Sex: FEMALEMin age: 20 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Female patients with endometriosis Exclusion Criteria: * Patients with clinically significant hepatic, renal, or cardiovascular dysfunction

Locations (1)

Japan

Tokyo and Other Japanese City, Japan

Outcomes

Primary Outcomes

The severity score of the pelvic pain

Time frame: 12 weeks

Data from ClinicalTrials.gov

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