While there are currently no marketed disease-modifying therapies (DMTs) for Parkinson’s disease (PD), hope is on the horizon in the shape of prasinezumab (PRX-002), Roche’s (ROG: SIX) monoclonal antibody.
The Swiss pharma giant has presented positive four-year results from a six-year open-label extension of the Phase II PASADENA trial evaluating the efficacy of the drug, which strengthen the hope that it will be able to slow PD motor progression, according to GlobalData, a data and analytics company.
"Recent results from the PASADENA extension greatly raises the anticipation for the conclusion of PADOVA, the ongoing Phase IIb trial"These results were presented at the American Academy of Neurology (AAN) 2024 annual meeting.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze