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If that argument implicitly limited the claim to excipients not disclosed in the prior art, a generic manufacturer using a different excipient may be able to design around the patent without triggering literal infringement, and prosecution history estoppel may prevent the infringement claim based on equivalents

Work with your healthcare provider to find the optimal dose that balances efficacy with tolerability

Medicare Resources: CMS has many useful publications

Further studies involving robust mechanistic validation, pharmacokinetic profiling, and clinical translation are essential to determine whether these compounds possess genuine therapeutic potential or if their effects are limited to experimental settings