- Prothena reported that partner presentations at AD/PD 2026 included clinical updates on prasinezumab for Parkinson’s disease and BMS-986446 for Alzheimer’s disease.
- Roche presented PASADENA open-label extension analyses that estimated about two years of “time saved” versus a model-based comparator, based on outcomes five years after trial start.
- Roche also presented additional PADOVA open-label extension data indicating a sustained effect on slowing Parkinson’s progression, and said the evidence informed initiation of the Phase III PARAISO study.
- Poster data from PADOVA described exploratory MRI biomarker findings, including slowed neuromelanin signal loss and reduced iron accumulation.
- Bristol Myers Squibb presented a randomized, double-blind, placebo-controlled study in healthy participants reporting single-dose BMS-986446 was safe and well tolerated, with no anti-drug antibodies detected.
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. Prothena Corporation plc published the original content used to generate this news brief via Business Wire (Ref. ID: 202603211605BIZWIRE_USPR_____20260321_BW254343) on March 21, 2026, and is solely responsible for the information contained therein.
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