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Buy Vegzelma (Bevacizumab-adcd)

Price range: €375.00 through €1,125.00

Description

What is Vegzelma (Bevacizumab-adcd)?

On September 28, the U.S. Food and Drug Administration (FDA) approved Bevacizumab-adcd (Vegzelma), a biosimilar to Bevacizumab (Avastin), for the treatment of six cancers: metastatic colorectal cancer; recurrent or metastatic non-squamous non-small cell lung cancer (NSCLC); recurrent glioblastoma; metastatic renal cell carcinoma; persistent, recurrent, or metastatic cervical cancer; and epithelial ovarian cancer, fallopian tube cancer, or primary peritoneal cancer.

Where was Vegzelma (bevacizumab-adcd) approved?

On September 28, the U.S. Food and Drug Administration (FDA) approved Bevacizumab-adcd (Vegzelma), a biosimilar to Bevacizumab (Avastin), for the treatment of six types of cancer: metastatic colorectal cancer, recurrent or metastatic non-small cell lung cancer (NSCLC), recurrent glioblastoma, metastatic renal cell carcinoma, persistent, recurrent or metastatic cervical cancer, and epithelial ovarian cancer, fallopian tube cancer, or primary peritoneal cancer.

The European Medicines Agency (EMA) decided that Vegzelma, in accordance with EU requirements for biosimilar medicines, has a very similar structure, purity, and biological activity to Avastin (an EMA-authorised medicine) and is distributed in the body in the same way. The data were deemed sufficient to conclude that Vegzelma performs in the same way as Avastin in terms of efficacy and safety in its authorized uses. Therefore, the Agency considered that, as with Avastin, the benefits of Vegzelma outweigh the identified risks and that the medicine could be authorised for use in the EU.

Additional information
Quantity

100 mg/4 mL (25 mg/mL)

,

400 mg/16 mL (25 mg/mL)

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