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TauRx Announces Completion of Phase 3 Study Enrolment for the First Tau-based Disease Modifying Treatment for Alzheimer's Disease

Published: 2021-01-11 09:19:00 ET

Aberdeen, Scotland and Singapore, Singapore--(Newsfile Corp. - January 11, 2021) - TauRx Pharmaceuticals Ltd today announced it has completed patient enrolment of the LUCIDITY study (NCT03446001) ahead of schedule, despite delays due to the COVID-19 pandemic. TauRx is pleased to be presenting its latest trial results at Biotech Showcase 2021 during the J.P. Morgan 39th Annual Healthcare Conference 2021. LUCIDITY is the only late-stage study targeting the tau pathology of Alzheimer's disease. It aims to confirm hydromethylthionine as the first tau-based disease modifying treatment for Mild Cognitive Impairment and Mild-Moderate AD.

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Key Takeaways:

TauRx Pharmaceuticals Ltd today announced it has completed patient enrolment of the LUCIDITY study (NCT03446001) ahead of schedule, despite delays due to the COVID-19 pandemic.
TauRx is pleased to be presenting its latest trial results at Biotech Showcase 2021 during the J.P. Morgan 39th Annual Healthcare Conference 2021.
If the efficacy of hydromethylthionine is confirmed, it will open up a completely new treatment direction for a devastating disease which has so far defied all efforts to bring it under control.

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Contacts:

TauRx Media r.andersen@taurx.com

Source: TauRx

To view the source version of this press release, please visit https://www.newsfilecorp.com/release/71720

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