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The research confirms that with proper administration by trained professionals, these treatments present minimal risks and deliver noticeable improvements

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Without rigorous testing, it's unknown if the compounds could have unintended, harmful effects, says Eileen Kennedy, a chemical biologist at the UNC Eshelman School of Pharmacy who studies peptide therapies

The FDA's 2025 guidance for biosimilars aims to cut development time and cost in half by replacing expensive human studies with advanced analytical testing in cases where the science supports it, which could accelerate future approvals