Alterity Therapeutics Announces Positive Results from Phase 2 Trial of ATH434 for Multiple System Atrophy

Reuters

07/28

<a href="https://laohu8.com/S/ATH.AU">Alterity Therapeutics</a> Announces Positive Results from Phase 2 Trial of ATH434 for Multiple System Atrophy

Alterity Therapeutics Ltd. has announced positive topline data from its open-label Phase 2 clinical trial of ATH434 in individuals with multiple system atrophy $(MSA)$. The ATH434-202 trial assessed a patient population with more advanced MSA compared to the cohort in the earlier double-blind Phase 2 trial, ATH434-201. The results demonstrated clinical benefits on the Unified MSA Rating Scale and global measures of neurological symptoms, with neuroimaging biomarkers indicating target engagement and slowed brain atrophy. ATH434 was well-tolerated and exhibited a favorable safety profile. These findings align with previous data from the Phase 2 double-blind trial and support the further advancement of ATH434 in the treatment of MSA. As of now, there are no disease-modifying medications available for MSA, making the development of ATH434 significant. The results have been presented and are consistent with Alterity's ongoing efforts to address neurodegenerative diseases.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Alterity Therapeutics Ltd. published the original content used to generate this news brief on July 28, 2025, and is solely responsible for the information contained therein.

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The ATH434-202 trial assessed a patient population with more advanced MSA compared to the cohort in the earlier double-blind Phase 2 trial, ATH434-201. The results demonstrated clinical benefits on the Unified MSA Rating Scale and global measures of neurological symptoms, with neuroimaging biomarkers indicating target engagement and slowed brain atrophy. ATH434 was well-tolerated and exhibited a favorable safety profile. These findings align with previous data from the Phase 2 double-blind trial and support the further advancement of ATH434 in the treatment of MSA. As of now, there are no disease-modifying medications available for MSA, making the development of ATH434 significant. The results have been presented and are consistent with Alterity's ongoing efforts to address neurodegenerative diseases.\n      </p>\n</div><div xmlns:xsd=\"http://www.w3.org/2001/XMLSchema\" xmlns:xsi=\"http://www.w3.org/2001/XMLSchema-instance\">\n<em>Disclaimer: <span>This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. 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The ATH434-202 trial assessed a patient population with more advanced MSA compared to the cohort in the earlier double-blind Phase 2 trial, ATH434-201. The results demonstrated clinical benefits on the Unified MSA Rating Scale and global measures of neurological symptoms, with neuroimaging biomarkers indicating target engagement and slowed brain atrophy. ATH434 was well-tolerated and exhibited a favorable safety profile. These findings align with previous data from the Phase 2 double-blind trial and support the further advancement of ATH434 in the treatment of MSA. As of now, there are no disease-modifying medications available for MSA, making the development of ATH434 significant. The results have been presented and are consistent with Alterity's ongoing efforts to address neurodegenerative diseases.\n      </p>\n</div><div xmlns:xsd=\"http://www.w3.org/2001/XMLSchema\" xmlns:xsi=\"http://www.w3.org/2001/XMLSchema-instance\">\n<em>Disclaimer: <span>This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Alterity Therapeutics Ltd. published the original content used to generate this news brief on July 28, 2025, and is solely responsible for the information contained therein.</span></em>\n</div></body></html>\n\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"ATH.AU","symbol_name":"ALTERITY THERAPEUTICS LTD","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250728:nNDL64s93X:1","article_id":"2554749516","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2554749516","pubTimestamp":1753661864,"columns":[],"sourceInfo":null,"weMediaInfo":{"media_name":"Reuters","introduction":"Reuters.com brings you the latest news from around the world, covering breaking news in markets, business, politics, entertainment and technology","home_visible":1,"id":"1032215980","head_image":"https://community-static.tradeup.com/news/4567337cbdf294b657b1fa87c5488b48"},"summary":"Alterity Therapeutics Ltd. has announced positive topline data from its open-label Phase 2 clinical trial of ATH434 in individuals with multiple system atrophy . The ATH434-202 trial assessed a patient population with more advanced MSA compared to the cohort in the earlier double-blind Phase 2 trial, ATH434-201. The results demonstrated clinical benefits on the Unified MSA Rating Scale and global measures of neurological symptoms, with neuroimaging biomarkers indicating target engagement and slowed brain atrophy. ATH434 was well-tolerated and exhibited a favorable safety profile. These findings align with previous data from the Phase 2 double-blind trial and support the further advancement of ATH434 in the treatment of MSA. As of now, there are no disease-modifying medications available for MSA, making the development of ATH434 significant. 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The results demonstrated clinical benefits on the Unified MSA Rating Scale and global measures of neurological symptoms, with neuroimaging biomarkers indicating target engagement and slowed brain atrophy. ATH434 was well-tolerated and exhibited a favorable safety profile. These findings align with previous data from the Phase 2 double-blind trial and support the further advancement of ATH434 in the treatment of MSA. As of now, there are no disease-modifying medications available for MSA, making the development of ATH434 significant. The results have been presented and are consistent with Alterity's ongoing efforts to address neurodegenerative diseases.\n      \n\nDisclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Alterity Therapeutics Ltd. published the original content used to generate this news brief on July 28, 2025, and is solely responsible for the information contained therein.","kind":"highlight","is_publish_news":true,"is_publish_highlight":false,"is_publish_live":false,"is_publish_wemedia":null,"editions":null,"column":"","sentiment":"2","news_tag":"dataReport","news_rank":0,"symbols":[],"gpt_button":0,"need_auth":false,"code":"91000000","status":"200"}}}