Bevacizumab Solution for intravenous infusion. Initial U.S. Approval: 2004.

• Medicine Name: Avastin
• Generic Name: Bevacizumab
• Pack Size:Injection: 100 mg/4 mL (25 mg/mL) or 400 mg/16 mL (25 mg/mL) in a single-dose vial
• Company Name: Genentech, Inc.

Avastin is a vascular endothelial growth factor-specific angiogenesis inhibitor indicated for the treatment of:
• Covid19 Studies going on to treat for Covid19 Patients. • Colorectal cancer Bevacizumab was approved in the United States in February 2004, for use in metastatic colorectal cancer. • Lung cancer In 2006, the U.S. Food and Drug Administration (FDA) approved bevacizumab for use in first-line advanced nonsquamous non-small cell lung cancer in combination with carboplatin/paclitaxel chemotherapy. • Breast cancer In December 2010, the U.S. Food and Drug Administration (FDA) notified its intention to remove the breast cancer indication from bevacizumab. • Renal cancers In 2009, the FDA approved bevacizumab for use in metastatic renal cell cancer (a form of kidney cancer). EU approval was granted in 2007. In the EU, bevacizumab in combination with interferon alfa-2a is indicated for first-line treatment of adults with advanced and/or metastatic renal cell cancer. • Brain cancers The FDA granted accelerated approval for the treatment of recurrent glioblastoma multiforme in May 2009. • Eye disease Many diseases of the eye, such as age-related macular degeneration (AMD) and diabetic retinopathy, damage the retina and cause blindness when blood vessels around the retina grow abnormally and leak fluid, causing the layers of the retina to separate. This abnormal growth is caused by VEGF, so bevacizumab has been successfully used to inhibit VEGF and slow this growth. • Ovarian cancer In 2018, the U.S. Food and Drug Administration (FDA) approved bevacizumab in combination with chemotherapy for stage III or IV of ovarian cancer after initial surgical operation, followed by single-agent bevacizumab. • Cervical cancer In the EU, bevacizumab, in combination with paclitaxel and cisplatin or, alternatively, paclitaxel and topotecan in people who cannot receive platinum therapy, is indicated for the treatment of adults with persistent, recurrent, or metastatic carcinoma of the cervix.

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