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Prothena Corporation (PRTA) investor relations material
Prothena Corporation Evercore ISI 8th Annual HealthCONx Conference summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Pipeline and program updates
Two phase III programs advancing: prasinezumab for early Parkinson's (with Roche) and coramitug for ATTR cardiomyopathy (with Novo), both with recent positive data and phase III initiations in late 2024.
Phase II Alzheimer's program targeting tau (with Bristol Myers Squibb) and phase I neurodegeneration program (X019) ongoing, with key data expected in 2027.
Unpartnered programs progressing, including PRX012 for Alzheimer's, with efforts to enhance blood-brain barrier penetration using transferrin technology.
Up to $105 million in clinical milestones anticipated in 2026 for coramitug enrollment; share repurchase program approved for 2026.
Additional data on CYTOPE and ALS program expected, following recent presentations.
Scientific and clinical insights
PRX012 shows robust amyloid reduction, with over 80% of patients amyloid negative at 18 months using subcutaneous monthly dosing.
ARIA rate for PRX012 is approximately 40%, with ongoing efforts to mitigate this effect, including exploring pre-symptomatic patient populations.
Transferrin-based brain shuttle technology may allow for a threefold dose reduction and potentially improved CNS distribution and ARIA profile.
FDA guidance may reduce preclinical requirements for novel molecular entities, with ongoing discussions about IND-enabling toxicology packages.
Fast-track status for tau-targeting phase II program reflects regulatory conviction in tau as a key Alzheimer's target.
Partnership and collaboration strategy
Strategic partnerships with Roche, Novo, and Bristol Myers Squibb drive late-stage programs, with active scientific and clinical collaboration.
Partner decisions to advance programs are based on rigorous internal criteria and recent compelling data, especially for prasinezumab and coramitug.
Support for partner programs includes scientific input and clinical trial execution, with more intensive involvement in early-stage studies.
Licensing and collaboration opportunities for transferrin-based anti-A beta antibodies depend on the strength of preclinical and clinical data.
Ongoing evaluation of deal value and timing for data disclosure to maximize partnership potential.
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