On 18 September 2024, the US Food and Drug Administration (FDA) granted approval for a second strength for Accord’s Hercessi (trastuzumab-strf), a biosimilar referencing Roche’s Herceptin.
FDA approves second strength of trastuzumab biosimilar Hercessi
Biosimilars/News | Posted 23/10/2024 0 Post your comment
Hercessi is now approved in a 420 mg strength to treat HER2-overexpressing breast and gastric or gastroesophageal junction adenocarcinoma. This news comes after the FDA approval of a 150 mg strength on 29 April 2024 [1].
The FDA’s approval of a second strength of Hercessi paves the way for Accord BioPharma to commercially launch its first biosimilar in the US in early 2025.
FDA approval for Hercessi was based on analytical, preclinical, and clinical data from three studies, showing it is similar to Herceptin (trastuzumab) in efficacy, safety, and quality. These included two Phase 1 pharmacokinetic (PK) studies in healthy volunteers (HLX02-HV01, HLX02-HV02) and a Phase 3 clinical study in patients with HER2-overexpressing metastatic breast cancer (HLX02-BC01). The data adhered to FDA biosimilar guidelines and showed no clinically meaningful differences in safety or efficacy between HERCESSI and Herceptin, supporting their biosimilarity.
Hercessi (HLX02) was originally developed by Accord's business partner, Shanghai Henlius Biotech, Inc, headquartered in Shanghai, China. In 2021, Henlius granted Accord BioPharma the exclusive rights to develop and commercialize Hercessi in the US and Canada.
Henlius’ trastuzumab biosimilar, Adheroza, was approved in Canada on 22 August 2024, and is also marketed by Accord [2].
Accord BioPharma, the US specialty division of Intas Pharmaceuticals Ltd, is focused on the development of oncology, immunology, and critical care therapies.
Related article
Advances for Henlius’ trastuzumab and bevacizumab biosimilars in the US
LATIN AMERICAN FORUM View the latest headline article: Un innovador acuerdo de compra directa permite reducir drásticamente los precios de los biosimilares de adalimumab Browse the news in the Latin American Forum! Register to receive the GaBI Latin American Forum newsletter. Inform colleagues and friends of this new initiative.
FORO LATINOAMERICANO Ver el último artículo de cabecera: Un innovador acuerdo de compra directa permite reducir drásticamente los precios de los biosimilares de adalimumab !Explore las noticias en el Foro Latinoamericano! Regístrese para recibir el boletín informativo GaBI Foro Latinoamericano. Informe a colegas y amigos sobre esta nueva iniciativa. |
References
1. GaBI Online - Generics and Biosimilars Initiative. FDA approves ustekinumab, trastuzumab, and tocilizumab biosimilars [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2024 Oct 23]. Available from: www.gabionline.net/biosimilars/news/fda-approves-ustekinumab-trastuzumab-and-tocilizumab-biosimilars
2. GaBI Online - Generics and Biosimilars Initiative. Canada approves trastuzumab Adheroza and ustekinumab Steqeyma biosimilars [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2024 Oct 23]. Available from: www.gabionline.net/biosimilars/news/canada-approves-trastuzumab-adheroza-and-ustekinumab-steqeyma-biosimilars
Permission granted to reproduce for personal and non-commercial use only. All other reproduction, copy or reprinting of all or part of any ‘Content’ found on this website is strictly prohibited without the prior consent of the publisher. Contact the publisher to obtain permission before redistributing.
Copyright – Unless otherwise stated all contents of this website are © 2024 Pro Pharma Communications International. All Rights Reserved.
Research
Long-term real-world safety experience of biosimilars confirms concept of biosimilarity
Budget impact analysis of Rixathon introduction in Chile for non-Hodgkin lymphoma
General
Biosimilar medicines on the Pharmaceutical Benefits Scheme in Australia
SBR issues consensus on interchangeability of reference products and biosimilars
Comments (0)
Post your comment