Price for Mustargen Rises Sharply With New Manufacturer

News broke today after the New York Times and other papers published a story on the sharp rise in cost for the drug Mustargen (Nitrogen Mustard). The drug was developed over 60 years ago and has been a mainstay for lymphoma treatment for most of that time.
It is a primary drug used to treat cutaneous (skin) T-cell lymphoma and Hodgkin's Lymphoma as part of the MOPP regimen used if ABVD chemotherapy cannot (or has failed).



The drug company Merck recently sold the rights to make and market Mustargen to Ovation Pharmaceuticals. Ovation has now raised the cost of the drug over 650%!



For those without insurance or others whose doctors use it for treatment not covered by insurance, the price increase will be nearly prohibitive.



The Times quotes Sean Nolan, vice president of commercial development for Ovation, as saying that the price increases were needed to invest in manufacturing facilities for the drugs. He said the company was petitioning insurers to obtain coverage for patients



But Merck is still making the drug for Ovation. There appears to be more to this. It is a disturbing trend in the small drug sector and lymphoma patients are taking the brunt of it.

Blog Category: 

More Articles

More Articles

Amazon.com is pleased to have the Lymphoma Information Network in the family of Amazon.com associates. We've agreed to ship items...

The question ought to be what are myelodysplastic syndromes (MDS), since this is a group of similar blood and bone marrow diseases that...

Merkel Cell Carcinoma (MCC) is a very rare and aggressive skin cancer that usually develops when a person is in his or her 70s. It is...

Radiation Therapy Topics

...

At some point, the Seattle biotech company Cell Therapeutics Inc (CTI) should earn an entry in the Guinness Book of World Records for utter and...

Site Beginnings

This site was started as Lymphoma Resource Page(s) in 1994. The site was designed to collect lymphoma...

Three papers appearing in the journal Blood and pointing towards a regulator-suppressor pill could offer hope to blood cancer...

The US Food and Drug Administration (FDA) has granted a third so-called Breakthrough Therapy Designation for the investigational oral...

The US Food and Drug Administration today has approved an expanded use of Imbruvica (ibrutinib) in patients with...

The U.S. Food and Drug Administration has announced that it has granted "Breakthrough Therapy Designation" for the investigational agent...

According to a new study published in the Proceedings of the National Academy of Sciences, a team from the University of California, San...

Pharmacyclics has announced that the company has submitted a New Drug Application (NDA) to the US Food and Drug Administration (FDA) for...

New research suggests that frontline radioimmunotherapy...

Gilead Sciences has announced results of the company's Phase II study of its investigational compound idelalisib, an oral inhibitor of...

Sitemap