Efficacy and Safety of TAK-385 in the Treatment of Uterine Fibroids

PHASE2CompletedINTERVENTIONAL
Enrollment

216

Participants

Timeline

Start Date

October 31, 2011

Primary Completion Date

September 30, 2012

Study Completion Date

September 30, 2012

Conditions
Uterine Fibroids
Interventions
DRUG

TAK-385

TAK-385 10 mg, tablets, orally, once daily for up to 12 weeks.

DRUG

TAK-385

TAK-385 20 mg, tablets, orally, once daily for up to 12 weeks.

DRUG

TAK-385

TAK-385 40 mg, tablets, orally, once daily for up to 12 weeks.

DRUG

Placebo

TAK-385 placebo-matching tablets, orally, once daily for up to 12 weeks.

Trial Locations (27)

Unknown

Chiba

Itchihara-shi

Matsuno-shi

Matsuyama

Nihama-shi

Fukui-shi

Fukuoka

Iizuka-shi

Yanagigawa-shi

Mebashi-shi

Ebetsu-shi

Sapporo

Amagasaki-shi

Kobe

Kamakura-shi

Yokohama

Ōita

Ibaraki-shi

Osaka

Sakai-shi

Tondabayashi-shi

Chuo-ku

Itabashi-ku

Setagaya-ku

Shinagawa-ku

Suginami-ku

Toyama

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Takeda

INDUSTRY