A Long Term Study To Evaluate The Safety, Tolerability And Efficacy Of CP-690,550 In Patients With Moderate To Severe Plaque Psoriasis And/Or Psoriatic Arthritis

PHASE3CompletedINTERVENTIONAL
Enrollment

95

Participants

Timeline

Start Date

March 31, 2012

Primary Completion Date

January 31, 2014

Study Completion Date

January 31, 2014

Conditions
Psoriasis
Interventions
DRUG

CP-690,550

10 mg BID, continuous treatment for 16 weeks under blinding, 10 mg BID, continuous treatment for 4 weeks and variable dose (5 mg or 10 mg), continuous treatment for 32 weeks.

DRUG

CP-690, 550

5 mg BID, continuous treatment for 16 weeks under blinding, 10 mg BID, continuous treatment for 4 weeks and variable dose (5 mg or 10 mg), continuous treatment for 32 weeks.

Trial Locations (16)

814-0180

Fukuoka University Hospital, Fukuoka

960-1295

Fukushima Medical University Hospital, Fukushima

060-0033

JR Sapporo hospital, Sapporo

650-0017

Kobe University Hospital, Chuo-ku, Kobe

920-0293

Kanazawa Medical University Hospital, Kahoku-gun

252-0392

National Hospital Organization Sagamihara National Hospital, Sagamihara

889-1692

University of Miyazaki Hospital, Miyazaki

550-0012

Nissay Hospital, Osaka

324-0498

Jichi Medical University Hospital, Shimotsuke

102-8798

Tokyo Teishin Hospital, Chiyoda-ku

193-0998

Tokyo medical university Hachioji medical center, Hachiōji

141-8625

Kanto Medical Center NTT East Corporation, Shinagawa-ku

160-0023

Tokyo Medical University Hospital, Shinjyuku-ku

939-1395

Tonami General Hospital, Tonami

400-8506

Yamanashi Prefectural Central Hospital, Kofu

105-8471

Jikei University Hospital, Tokyo

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY

NCT01519089 - A Long Term Study To Evaluate The Safety, Tolerability And Efficacy Of CP-690,550 In Patients With Moderate To Severe Plaque Psoriasis And/Or Psoriatic Arthritis | Biotech Hunter | Biotech Hunter