Drug Topics August 8, 2024
Lauren Massaro

In a clinical trial, IPX203 was able to achieve longer good on-time with less doses compared to standard treatment.

Amneal Pharmaceuticals announced that the FDA has approved its extended-release carbidopa and levodopa (CD/LD, [IPX203]) capsules, marketed as Crexont, for the treatment of Parkinson’s disease, according to a company news release.1

As Parkinson’s disease progresses, patients often experience increased motor fluctuations and reduced “good on-time,” defined as periods without troublesome dyskinesia.1 Whereas existing immediate-release CD/LD products are short-acting, Amneal’s IPX203 combines immediate-release granules and extended-release pellets to provide rapid onset of action and long-lasting efficacy, respectively.

“The approval of Crexont is a seminal moment in the treatment paradigm for PD. The burden of this incurable neurodegenerative disease increases with time....

Today's Sponsors

Venturous
Got healthcare questions? Just ask Transcarent

Today's Sponsor

Venturous

 
Topics: Biotechnology, Clinical Trials, FDA, Govt Agencies, Patient / Consumer, Pharma, Pharma / Biotech, Provider, Trends
Amgen starts two critical late-stage trials for weight loss drug MariTide
Patient Access To Cheaper Biosimilar Drugs Varies Significantly Across Pharmacy Benefit Managers
Novo Nordisk offers Wegovy for less than half the price through new direct-to-consumer pharmacy
'Not just adding another drug to your pharmacy': CAR T, explained
Private equity firm to buy Walgreens for $10B, report says

Share This Article