By Mariam Sunny
Dec 9 (Reuters) - AbbVie's ( ABBV ) experimental drug to
treat early Parkinson's disease helped significantly improve
patients' ability to carry out daily tasks such as eating and
walking, months after the drugmaker disclosed its success in a
separate study.
The late-stage study tested the safety and efficacy of
flexible doses of the once-daily drug, tavapadon, ranging from 5
milligrams (mg) to 15 mg, as a monotherapy, the company said on
Monday.
AbbVie ( ABBV ) acquired the drug through its $8.7 billion purchase
of Cerevel Therapeutics last year as its rheumatoid arthritis
drug Humira, once the world's best-selling treatment, faces a
sharp fall in sales due to competition from close copies.
"Although questions remain on tavapadon's competitive
profile, this shows at least some payoff for the Cerevel
transaction," said Piper Sandler analyst Christopher Raymond.
More than $40 billion was wiped off from AbbVie's ( ABBV ) market
value last month after a schizophrenia drug acquired through the
Cerevel deal failed in two separate studies.
In September, two fixed doses of tavapadon as a monotherapy
had shown significant improvement in patients in a late-stage
study.
The majority of side effects reported, such as nausea,
headache, and dry mouth, were mild to moderate in severity.
AbbVie ( ABBV ) plans to submit a marketing application to the U.S.
Food & Drug Administration next year.
The study enrolled 304 adults between the ages of 40 and 80,
who had the disease for less than three years.
There are an estimated 1 million people in the U.S. living
with Parkinson's, a progressive neurological disorder that
impairs the brain's nerve cells, thereby affecting the
production of dopamine, a neurotransmitter that regulates
functions such as memory, movement, and mood.
There is no known cure for the disease, and available
treatments only help alleviate symptoms.
The established standard of care for the disease, levodopa,
acts as a dopamine replacement agent. Tavapadon belongs to a
class of drugs known as dopamine agonists, which activate the
dopamine receptors.
(Reporting by Mariam Sunny in Bengaluru; Editing by Anil
D'Silva and Sriraj Kalluvila)