Multi-center, randomized , double-blind, placebo-controlled , two arm parallel design study of NeuroVax™ vs. Incomplete Freund's Adjuvant ( I F A) placebo. 150 subjects with Secondary Progressive SPMS.
The primary objective is to compare between treatment groups the Measures of neurologic disability EDSS scores.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
150
NeuroVax consists of a Trivalent TCR Peptide Formulation in IFA
IFA Placebo Incomplete Freund's Adjuvant
CRO
San Diego, California, United States
The primary objective is to compare between treatment groups the Measures of neurologic disability EDSS score
The primary objective is to compare between treatment groups the Measures of neurologic disability EDSS scores improvements
Time frame: 48 Weeks
Secondary measurements objectives immunologic evaluations
Secondary measurements objectives immunologic evaluations increases in white blood cell counts \& FOXP+3 expression increases
Time frame: 48 Weeks
Richard Bartholomew
CONTACT
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.