An Approach to Mitigate Particle Formation on the Dilution of a Monoclonal Antibody Drug Product in an IV Administration Fluid

J Pharm Sci. 2016 Mar;105(3):1349-50. doi: 10.1016/j.xphs.2015.12.013. Epub 2016 Jan 30.

Abstract

To support dose reduction, low dose of a monoclonal antibody (mAb) was required to be administered via IV infusion at a concentration of 0.1 mg/mL. To achieve the target protein concentration, the infusion solution was prepared by diluting the drug product containing 10-mg/mL mAb with normal saline, a 0.9% sodium chloride injection solution. However, particles were observed in the diluted solution. Particle formation must be avoided to administer the low dose using the existing drug product. To mitigate the particle formation, an unconventional compounding approach was used. With this approach, a stabilizing vehicle containing polysorbate-80 was added to saline before drug-product dilution to maintain suitable surfactant level to prevent precipitation of the mAb. In this way, use of the stabilizing vehicle to support low doses ensured suitable quality across a wider range of mAb concentrations, thereby allowing additional flexibility to the clinical trial. Such an approach may be useful for broader application in early-stage clinical trials where there is an uncertainty regarding doses or the need to revise to lower doses based on clinical observations or other drivers.

Keywords: precipitation; preformulation; protein aggregation; protein formulation; protein structure.

MeSH terms

  • Antibodies, Monoclonal / administration & dosage*
  • Antibodies, Monoclonal / chemistry*
  • Chemistry, Pharmaceutical / methods
  • Clinical Trials as Topic
  • Drug Stability
  • Excipients / chemistry
  • Infusions, Intravenous / methods
  • Pharmaceutical Solutions / administration & dosage*
  • Pharmaceutical Solutions / chemistry
  • Polysorbates / chemistry
  • Surface-Active Agents / chemistry

Substances

  • Antibodies, Monoclonal
  • Excipients
  • Pharmaceutical Solutions
  • Polysorbates
  • Surface-Active Agents