A Multiple Dose Study Of PD-0360324 In Patients With Active Cutaneous Lupus Erythematosus

PHASE1TerminatedINTERVENTIONAL
Enrollment

28

Participants

Timeline

Start Date

November 30, 2011

Primary Completion Date

November 30, 2013

Study Completion Date

November 30, 2013

Conditions
Cutaneous Lupus Erythematosus
Interventions
DRUG

PD-0360324

Subjects will receive PD-0360324 intravenously in 3 different cohorts. The cohorts will be evaluated in ascending fashion. The doses planned are 100 mg every other week for 3 months, 150 mg every other week for 3 months, and 200 mg every 4 weeks for 3 months.

DRUG

Placebo

Placebo is normal saline. The timing of placebo administration will depend of the dosing frequency of the cohort (either every other week for 3 months or every 4 weeks for 3 months).

Trial Locations (19)

2025

Pfizer Investigational Site, Chisinau

16635

Pfizer Investigational Site, Ducansville

19107

Pfizer Investigational Site, Philadelphia

19610

Pfizer Investigational Site, Wyomissing

23507

Pfizer Investigational Site, Norfolk

26301

Pfizer Investigational Site, Clarksburg

28210

Pfizer Investigational Site, Charlotte

32073

Pfizer Investigational Site, Orange Park

36203

Pfizer Investigational Site, Oxford

36207

Pfizer Investigational Site, Anniston

38305

Pfizer Investigational Site, Jackson

46256

Pfizer Investigational Site, Indianapolis

48059

Pfizer Investigational Site, Fort Gratiot

57701

Pfizer Investigational Site, Rapid City

57702

Pfizer Investigational Site, Rapid City

60611

Pfizer Investigational Site, Chicago

75246

Pfizer Investigational Site, Dallas

90045

Pfizer Investigational Site, Los Angeles

L3P 1A8

Pfizer Investigational Site, Markham

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY

NCT01470313 - A Multiple Dose Study Of PD-0360324 In Patients With Active Cutaneous Lupus Erythematosus | Biotech Hunter | Biotech Hunter