FDA Publishes Immunogenicity Guidelines For Biosimilar Insulins

Biosimilar Insulins Generally Will Not Need Comparative Clinical Immunogenicity Data

In a move that will likely be welcomed by industry, the US FDA has issued draft guidance stating that sponsors will generally not need to conduct comparative clinical immunogenicity studies in developing biosimilar/interchangeable products.

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The US FDA is proposing streamlining development of biosimilar/interchangeable insulins • Source: Shutterstock

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