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Alterity Therapeutics

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21.01.2022 This new patent in the US supports the expansion of our next generation drug development portfolio focused on #NeurodegenerativeDisease

18.01.2022 International Clinical Trials Day is May 20th. We salute the wonderful patients, investigators and staff who make research happen around the world each and every day! #ICTD2020 #clinicaltrials #internationalclinicaltrialsday #clinicalresearch

18.01.2022 Gratifying to see the buzz around our announcement earlier this week!

16.01.2022 Our small molecule has been featured in the publication Neurology Today as part of the American Academy of Neurology 2020 Science Highlights. Although the AAN Annual Meeting was cancelled this year due to the global COVID-19 pandemic, research and development of new therapies for unmet medical needs such as Multiple System Atrophy continues. #MSA #MultipleSystemAtrophy #MovementDisorders #neurology

16.01.2022 Congratulations to David Stamler on his appointment to CEO! His succession aligns with the next phase of Alterity’s commercial strategy and comes at a time when the company is preparing to advance its lead compound ATH434 to Phase 2 clinical trials.

15.01.2022 October 3 is World MSA Day. We invite you to join us, MSA Belgium (the founder of World MSA Day), The Multiple System Atrophy Coalition and organizations around the world in lighting a candle at 8pm in your local time zone, to help build an unbroken chain of light that unites all of us in the fight against MSA. #worldmsaday #MSA #multiplesystematrophy

11.01.2022 Close to one million people in the US have a diagnosis of Parkinson’s disease (PD). Some who feel the diagnosis just doesn't seem right may in fact have multiple system atrophy (MSA).

08.01.2022 We are pleased to announce that PBT434 has now been granted orphan designation in both the US and EU for the treatment of Multiple System Atrophy #PBT434 #MSA #orphandrug #orphandesignation

08.01.2022 Our oral presentation on #ATH434 (formerly PBT434) for the treatment of Multiple System Atrophy is now available on the American Academy of Neurology virtual annual meeting platform. The platform is open to the public and the presentation can be accessed by clicking through here: #AAN #MSA #neurology #MovementDisorders

08.01.2022 #RareDiseaseDay is February 29, 2020, the rarest day of the year! Alterity stands in support of those living with rare diseases such as #MultipleSystemAtrophy as we work to develop new treatment options for people with MSA. Join us in supporting the rare disease community and #ShowYourStripes!

08.01.2022 Have you seen our recent announcement? Click through to read about the latest development news for ATH434.

07.01.2022 A fascinating peek into dysautonomia (dysfunction of the autonomic nervous system). Neurological symptoms associated with dysautonomia are a daily struggle for people living with conditions such as MSA.

05.01.2022 We are thrilled to embark on this important study with Vanderbilt University Medical Center. We hope the study will expand the field's understanding of #multiplesystematrophy and provide the foundation for advancing treatments such as #ATH434 into the clinic. Click below to read our press release: . #MSA #neurodegeneration

03.01.2022 We are in awe of all family caregivers and the sacrifices they make for their loved ones #caringforthecaregiver

02.01.2022 Alterity is proud to help sponsor the 2020 MSA Coalition Annual Patient & Family Conference! This year the conference is virtual and registration is free for MSA patients and their families. See below for registration link:

02.01.2022 As MSA Awareness Month comes to a close, we'd like to share this short film which captures the spirit and hope embodied by everyone we have met in the MSA community. You inspire us. "Fighting MSA: Austin Crawford's Story" was sponsored by the MSA Coalition and recently won the award for Best Documentary at the 2020 Tonkawa Film Festival. #MSAawarenessmonth #MSAawareness #fightMSA #richestmanintheworld