Accord BioPharma, the speciality division of , has received US Food and Drug Administration (FDA) approval for 420mg HERCESSI (trastuzumab-strf), a biosimilar to reference product Herceptin (trastuzumab) to treat HER2-overexpressing cancers. The approval will enable the commercial launch of the company’s first biosimilar in the US market, projected for early 2025. The gold standard of business intelligence.
HERCESSI is approved as an adjuvant treatment for adults with HER2-overexpressing breast cancer, metastatic breast cancer and metastatic gastric or gastroesophageal junction adenocarcinoma. HER2 cancers are aggressive and have been shown to respond effectively to targeted treatments such as HERCESSI, which inhibits the HER2 receptor to slow cell replication. The FDA’s decision was based on a comprehensive package of analytical, preclinical and clinical data from three studies.
These studies demonstrated that HERCESSI and Herceptin are similar in terms of efficacy, safety and quality. Access the most comprehensive Company Profiles on the market, powered by GlobalData. Save hours of research.
Gain competitive edge. Your download email will arrive shortly We are confident about the unique quality of our Company Profiles. However, we want you to make the most beneficial decision for your business, so we offer a free sample that you can download by submitting the below form The data included results from two Phase I comparative single-dose pharmacokinetic trials in healthy .