Ascendis Pharma Reports 3-Year Renal Benefits of TransCon PTH in Hypoparathyroidism

Reuters

2025/11/04

Ascendis Pharma Reports 3-Year Renal Benefits of TransCon PTH in Hypoparathyroidism

Ascendis Pharma A/S has announced that data from its Phase 2 PaTH Forward and Phase 3 PaTHway trials evaluating TransCon® PTH (palopegteriparatide) in adults with chronic hypoparathyroidism will be presented at Kidney Week 2025, held by the American Society for Nephrology in Houston from November 5-9. The three-year results demonstrate sustained improvements in renal function, continued normalization of urine calcium handling, and ongoing safety and efficacy with TransCon PTH treatment. The data will be presented on November 6 by Dr. Elvira Gosmanova, and the abstract is also available in the Journal of the American Society of Nephrology, October 2025 edition. TransCon PTH is approved as YORVIPATH® in the United States, European Union, and European Economic Area for adults with hypoparathyroidism.

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. Ascendis Pharma A/S published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9567650-en) on November 03, 2025, and is solely responsible for the information contained therein.

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Ascendis Pharma A/S published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9567650-en) on November 03, 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":"BK4139","symbol_name":"生物科技","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251103:nNDLcWZXn:1","article_id":"2580240127","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2580240127","pubTimestamp":1762203680,"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":"Disclaimer: This news brief was created by Public Technologies  using generative artificial intelligence. 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The three-year results demonstrate sustained improvements in renal function, continued normalization of urine calcium handling, and ongoing safety and efficacy with TransCon PTH treatment. The data will be presented on November 6 by Dr. Elvira Gosmanova, and the abstract is also available in the Journal of the American Society of Nephrology, October 2025 edition. TransCon PTH is approved as YORVIPATH® in the United States, European Union, and European Economic Area for adults with hypoparathyroidism.\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. Ascendis Pharma A/S published the original content used to generate this news brief via GlobeNewswire (Ref. 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