Pfizer inflammatory bowel disease drug wins EU approval


Add Pfizer's comment in paragraph 5

Feb 19 (Reuters) - Pfizer's PFE.N drug to treat patients with an inflammatory bowel disease called ulcerative colitis has been approved by the European Commission, the company said on Monday.

The approval for Velsipity follows backing from the European Medicines Agency's panel of experts in December.

The drug was approved for use in patients aged 16 or older and who did not show adequate response or were intolerant to previous treatment, Pfizer said.

The approval, applicable in all 27 countries of the European Union, is based on studies from two late-stage trials that showed the drug was effective and safe in eligible patients.

Pfizer said Velsipity will be available in each of the member countries after the national processes are complete, including applications for reimbursement for the drug.

About 2.6 million people in Europe are living with ulcerative colitis, Pfizer says.

Velsipity, which was approved in the United States in October, belongs to a class of drugs used to regulate the body's immune response and is expected to compete with Bristol Myers Squibb's BMY.N Zeposia.

Pfizer has also sought regulatory approvals for the drug in Australia, India and the UK, among others.

Leerink Partners in October estimated the drug's 2030 sales at $2.2 billion.

(Reporting by Leroy Leo in Bengaluru Editing by Jason Neely, David Goodman and David Evans)

(( ;;))

The views and opinions expressed herein are the views and opinions of the author and do not necessarily reflect those of Nasdaq, Inc.


More Related Articles

Info icon

This data feed is not available at this time.

Sign up for the TradeTalks newsletter to receive your weekly dose of trading news, trends and education. Delivered Wednesdays.