Commercial Novo Nordisk to Invest $1.2 Billion in New Rare...

Novo Nordisk to Invest $1.2 Billion in New Rare Disease Drug Facility in Denmark

-

Danish pharmaceutical giant Novo Nordisk announced plans to invest 8.5 billion Danish crowns ($1.2 billion) in a new facility in Odense, Denmark, dedicated to producing rare disease drugs.
The site will manufacture various therapies for rare diseases, including treatments for hemophilia, according to a statement released on Monday. In addition to a factory, the facility will include a warehouse to support operations.

Novo Nordisk, now Europe’s most valuable publicly listed company thanks to the success of its weight-loss injection Wegovy, acquired the 200-acre site in July. At the time, the company hinted at plans for a new plant but did not specify the type of drugs it would produce.
Earlier reports from Reuters, citing an environmental report Novo Nordisk submitted to Danish authorities in January, indicated the site would include facilities for “fill-finish” processes—used to fill injection pens. However, a company spokesperson clarified that while the factory will handle “finish” work such as packaging, it will not be involved in filling injection pens for drugs like Wegovy. The spokesperson emphasized that the facility will focus exclusively on rare disease treatments for the foreseeable future.
This marks Novo Nordisk’s first facility in Odense and its first new factory in Denmark in over two decades. Construction is already underway and is expected to conclude by 2027. Once operational, the facility will create 400 permanent jobs, with up to 1,000 external employees working on-site during the construction phase.

Novo Nordisk has announced several major investments this year, including a $4.1 billion plan to build a U.S. facility for filling injection pens for Wegovy and diabetes drug Ozempic.
Meanwhile, competition in the weight-loss drug market remains intense. In the UK, more Britons are opting for Eli Lilly’s Mounjaro when paying privately for obesity treatments.

+ posts

Latest news

Pfizer Decides Against Pursuing Lead Obesity Asset Amid Liver Safety Concerns

Pfizer said that it had discovered a possible instance of medication-induced liver impairment and, as a result, would no...

Vanda Challenges FDA Over Limits on Off-Label Drug Communication

Vanda Pharmaceuticals is pushing back against the U.S. Food and Drug Administration (FDA), accusing the agency of stifling the...

Life Sciences Voice Top Five Newsletter

Welcome to this week’s edition of the Life Sciences Voice Top Five Newsletter, your go-to source for the latest...

Must read

Surrounded by controversy, FDA approves Biogen’s Alzheimer’s drug Aduhelm

In the middle of the debate about the Alzheimer’s drug approval, the United States FDA has authorized Aduhelm

You might also likeRELATED
Recommended to you