US drugmaker Amneal Pharmaceuticals (NYSE: AMRX) has recently announced that its pipeline product IPX-203 (carbidopa + levodopa, (CD/LD)) achieved key primary and secondary endpoints in the pivotal Phase III RISE-PD clinical trial for patients with Parkinson’s disease (PD) who experience motor fluctuations.
Levodopa’s short half-life makes dosing difficult to manage and the treatment is often associated with dyskinesia and the medicine’s wearing-off episodes. The market for new products aimed at controlling motor fluctuations holds great potential, says GlobalData, a leading data and analytics company.
“Levodopa has been the gold standard of care for patients with PD for over 50 years. However, the decline in efficacy of levodopa and the emergence of motor fluctuations after a few years of its use remains a major challenge for physicians and patients,” commented GlobalData’s pharma analyst Christie Wong.
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