NICE Green Lights Pixantrone in UK

The independent body responsible for driving improvement and excellence in the health and social care system in the United Kingdom has given the green light for pixantrone as a treatment for some B-cell non-Hodgkin's lymphomas.

The National Institute for Health and Care Excellence (NICE), which "develops guidance, standards and information on high-quality health and social care" in the UK, has given the green light in final draft guidance for Cell Therapeutics' pixantrone (Pixuvri) following the lead set by the European Commission.

Stipulations of the recommendation

According to NICE, the drug should be funded by the National Health Services (NHS) to treat certain people with aggressive non-Hodgkin's B-cell lymphoma.

However, the recommendation comes with a few caveats:

  • - Patients must have relapsed or refractory disease.
  • - Patients must have received rituximab as treatment previously.
  • - This must be in the third or fourth line setting.

According to the recommendation, pixantrone is being made available for funding on the condition that Cell Therapeutics provides it at a discounted rate.

Why pixantrone has not been FDA-approved

The U.S. Food and Drug Administration has not approved pixantrone for the U.S. market – and currently shows no signs of doing so, largely due to incomplete and unimpressive clinical trial data.

Source: NICE

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