A Study of JNS020QD in Patients With Chronic Pain

PHASE3CompletedINTERVENTIONAL
Enrollment

77

Participants

Timeline

Start Date

October 31, 2011

Primary Completion Date

March 31, 2013

Study Completion Date

March 31, 2013

Conditions
Chronic Pain
Interventions
DRUG

JNS020QD

During weeks 1-3, initial doses of 0.84 mg, 1.7 mg, 3.4 mg, or 5 mg can be increased until individual optimal dose (up to maximum 20.1 mg) is determined. The optimal dose will be administered during the maintenance period (1 week), followed by a long-term treatment (48 weeks) period, where the dose will be adjusted (escalated or reduced) in consideration of the efficacy of the study, and the condition of adverse events. The patches are applied on the skin and exchanged daily (every 24 hours) for consecutive 52 weeks.

Trial Locations (18)

Unknown

Asahikawa

Chiba

Isesaki

Izumo

Kawasaki

Kobe

Matsumoto

Nishinomiya

Ohtsu

Okayama

Osaka

Saga

Sagamihara

Sapporo

Sendai

Toyama

Yamagata

Yamaguchi

Sponsors
All Listed Sponsors
lead

Janssen Pharmaceutical K.K.

INDUSTRY