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Dated 6th of June 2025 - TauRx can confirm it has completed the request for information (RFI) received from the Medicines and Healthcare products Regulatory Agency (MHRA) in relation to its UK Marketing Authorisation Application (MAA) for hydromethylthionine mesylate (HMTM). The only oral tau therapeutic to have completed Phase 3 trials, research suggests that if it is approved by regulators HMTM could slow the progression of Alzheimer’s disease – providing a major step forward in neurodegenerative disease research.
The company is committed to working with the MHRA and other bodies to address one of the world’s greatest unmet medical needs and eagerly awaits the outcome of the review.
Further updates on the application will be provided when appropriate.

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