Results of a phase I study in patients suffering from secondary-progressive multiple sclerosis demonstrating the safety of the amino acid copolymer PI-2301 and a possible induction of an anti-inflammatory cytokine response

J Neuroimmunol. 2010 Aug 25;225(1-2):153-63. doi: 10.1016/j.jneuroim.2010.04.008. Epub 2010 May 13.

Abstract

PI-2301 is an immunomodulator that could be an alternative therapy for MS. A placebo-controlled, multiple-ascending dose, double-blind study was performed in patients with secondary-progressive MS. Treatment was given subcutaneously once weekly for 8 weeks, followed by a 4-week open-label treatment period with active drug. The most common adverse event was transient injection site reactions. Non-significant trend for increases in serum levels of IL-3, IL-13, and CCL22 over time were suggestive of a beneficial T(H)2 immune response in subjects dosed with PI-2301 at 3 and 10 mg. MRI data indicated a non-significant trend for a reduction of lesion numbers in subjects treated with 1 and 3 mg PI-2301.

Publication types

  • Clinical Trial, Phase I
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Anti-Inflammatory Agents / blood
  • Anti-Inflammatory Agents / therapeutic use
  • Antibodies / blood
  • Cytokines / metabolism*
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Female
  • Glatiramer Acetate
  • Humans
  • Magnetic Resonance Imaging / methods
  • Male
  • Middle Aged
  • Multiple Sclerosis, Chronic Progressive / drug therapy*
  • Multiple Sclerosis, Chronic Progressive / immunology*
  • Peptides / immunology
  • Peptides / therapeutic use*
  • Severity of Illness Index
  • Th2 Cells / drug effects*
  • Treatment Outcome

Substances

  • Anti-Inflammatory Agents
  • Antibodies
  • Cytokines
  • Peptides
  • Glatiramer Acetate