A Phase 2 Study of Tapentadol Extended-Release (JNS024ER) ) in Japanese Participants With Chronic Pain Due to Diabetic Neuropathic Pain or Postherpetic Neuralgia

PHASE2CompletedINTERVENTIONAL
Enrollment

91

Participants

Timeline

Start Date

June 30, 2010

Primary Completion Date

April 30, 2011

Study Completion Date

April 30, 2011

Conditions
PainDiabetic NeuropathiesNeuralgiaPostherpetic Neuralgia
Interventions
DRUG

Tapentadol

Tapentadol hydrochloride extended-release(ER) will be administered as oral tablet at dose ranging from 25 milligram (mg) to 250 mg twice daily for 12 weeks.

DRUG

Placebo

Matching Placebo will be administered as oral tablet at dose ranging from 25 mg to 250 mg twice daily for 12 weeks.

Trial Locations (31)

Unknown

Chigasaki

Chūōku

Fukuoka

Inashiki

Isesaki

Izumisano

Kanuma

Katsushika-ku

Kawaguchi

kooriyama

Kurume

Kyoto

Matsue

Matsumoto

Minatoku

Mitaka

Nagano

Nagoya

Obihiro

Ohta-Ku

Ohtsu

Okayama

Omuta

Osaka

Sapporo

Sendai

Setagaya City

Shimotsuga

Tokyo

Ube

Yokohama

Sponsors
All Listed Sponsors
lead

Janssen Pharmaceutical K.K.

INDUSTRY