A Study To Evaluate The Safety And Tolerability Of PF-06342674 (RN168) In Subjects With Multiple Sclerosis (MS)

PHASE1TerminatedINTERVENTIONAL
Enrollment

4

Participants

Timeline

Start Date

September 30, 2014

Primary Completion Date

October 31, 2015

Study Completion Date

October 31, 2015

Conditions
Multiple Sclerosis
Interventions
BIOLOGICAL

PF-06342674 0.25 mg/kg

Bi-Weekly Subcutaneous Injections X 6

BIOLOGICAL

Placebo

Bi-Weekly Subcutaneous Injections X 6

BIOLOGICAL

PF-06342674 1.5 mg/kg

Bi-Weekly Subcutaneous Injections X 6

BIOLOGICAL

PF-06342674 6.0 mg/kg

Bi-Weekly Subcutaneous Injections X 6

Trial Locations (8)

12110

Fallon Wellness Pharmacy, Latham

Northeast Eye Center, Latham

The MS Center of Northeastern New York, Latham

12205

Albany Advanced Imaging, Albany

44195

Cleveland Clinic, Cleveland

73013

Retina Vitreous Center, Edmond

73112

Lynn Health Science Institute, Oklahoma City

Radiology Associates (X-ray facility only), Oklahoma City

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY