Clinical and Laboratory Standards Institute document I/LA34-A--Design and Validation of Immunoassays for Assessment of
Human Allergenicity of New Biotherapeutic Drugs; Approved Guideline provides a framework for the design and validation of a
qualitative immunoassay that detects human immunoglobulin E (IgE) antibody to new drugs in various body fluids and tissue
extracts. It addresses technical challenges that are uniquely associated with the development of an assay that detects drug-specific
IgE antibody in human blood and tissue extracts. It provides an approach for validation of an assay in the absence of a positive
drug-specific human IgE antibody serum, which involves a feasibility study phase and then development and validation, using a
concomitantly established drug-specific human immunoglobulin G antibody assay as part of its quality control program. This
guideline is intended for use by clinical and laboratory investigators who are involved in generating preclinical data and
performing clinical trials involving new biotherapeutic drugs. It is also intended as a guideline for administrators of manufacturer
safety programs, and government regulators who are required to critique IgE antibody assay methods and assess the validity of
allergenicity data that have been submitted by innovator pharmaceutical investigators as part of a governmental licensing process
for a new drug.
| ISBN(s) : | 1562387553 |
| Number of Pages : | 64 |
| Published : | 06/01/2011 |
