Part II of a series on these new agents
As noted in part I, a biosimilar is a biological product that is “biosimilar” to or “interchangeable” with an FDA-licensed biological product. These agents have been available in Europe for several years but are not yet available in the U.S. On 1/7/15, a 14-member expert panel unanimously recommended that the FDA approves EP2006, which is a close copy of filgrastim (Neupogen). EP2006 was approved in Europe in 2009 as Zarzio but has not been used in the U.S., in part because no regulatory pathway exists to approve biosimilars in the U.S.
If the FDA accepts the panel’s recommendation, it would open the door for producing biosimilars in the U.S., which are typically less expensive than the already-approved biologic agents. The savings in drug costs would be significant. According to the New York Times, Express Scripts notes biosimilars are about a third less expensive than brand-name biologic drugs in countries where they are in use and the cost savings may be significant for both the insurer as well as the patient.
FDA Approves Encorafenib Plus Cetuximab and Chemo in BRAF V600E-Positive Metastatic CRC
Published: December 20th 2024 | Updated: December 20th 2024The FDA has granted approval for the use of encorafenib in combination with cetuximab and mFOLFOX6 for the treatment of metastatic colorectal cancer harboring a BRAF V600E mutation.