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Sarah Yim, director of the Office of Therapeutic Biologics and Biosimilars in the FDAs Center for Drug Evaluation and Research, said in a Todays approval of the first biosimilar product indicated to treat relapsing forms of multiple sclerosis furthers the FDAs longstanding commitment to support a competitive marketplace for biological products and ultimately empowers patients by helping to increase access to safe, effective and high-quality medications at potentially lower cost. This approval could mark the start of wider access to a more cost-effective treatment for people with relapsing forms of MS.

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As investigations continue to uncover their multifaceted impacts, BPC-157 and TB-500 hold significant promise for advancing regenerative medicine and injury recovery