On Wednesday, August 30th, the FDA announced the approval of Sandoz’s Erelzi™ (etanercept-szzs). Erelzi is biosimilar to Amgen’s Enbrel® (etanercept) and is indicated for the treatment of multiple inflammatory diseases.
Erelzi is the third biosimilar product approved by the FDA. The product is administered by injection for the treatment of all five of Enbrel’s indications, which include:
According to an article from Biopharma-Reporter, a spokesman from Sandoz stated that the company “is fully committed to bringing Erelzi to US patients and payors ASAP.” However, Sandoz is required to give Amgen a minimum of 180-days’ notice before launching the product commercially, meaning that Erelzi could be available as early as February of 2017.
In its announcement, FDA stresses the fact that Erelzi has been approved as a biosimilar to Enbrel, not as an interchangeable product. This means that a pharmacist cannot substitute Erelzi for Enbrel without permission from the healthcare provider who originally prescribed Enbrel. Both Zarxio™ and Inflectra™ , the only other two biosimilar products approved in the US, have also been deemed to be biosimilar but not interchangeable.
The industry continues to wait for clarification from the FDA regarding how to prove a product is interchangeable. It will be interesting to watch as FDA provides this information, and as the first products are deemed interchangeable and additional products are approved as biosimilar.
April 27, 2017
On Friday, April 21st, Reneflexis® (SB2, infliximab – abda) was approved by the FDA. Reneflexis is manufactured by Samsung Bioeipis, and is a biosimilar product to Janssen’s Remicade® (infliximab). ...
April 7, 2016
On Tuesday, April 5th, FDA announced the approval of Inflectra™ (infliximab-dyyb), a biosimilar version of Janssen Biotech’s Remicade® (infliximab), for a number of indications. Inflectra is...
November 24, 2015
Recently, biosimilars have made a definite appearance on the FDA’s radar, an expected result after the first biosimilar product gained FDA approval in March and the FDA’s release of four final...