Vegzelma (bevacizumab-adcd) vs Elahere (mirvetuximab soravtansine-gynx)

Vegzelma (bevacizumab-adcd) vs Elahere (mirvetuximab soravtansine-gynx)

Vegzelma (bevacizumab-adcd) is a biosimilar to Avastin, which is a monoclonal antibody that inhibits vascular endothelial growth factor (VEGF), used primarily to treat various types of cancers, including colorectal, lung, glioblastoma, kidney, and ovarian cancer by preventing the growth of blood vessels that feed tumors. Elahere (mirvetuximab soravtansine-gynx) is an antibody-drug conjugate targeting the folate receptor alpha, which is frequently overexpressed in ovarian cancer cells, and it is specifically indicated for the treatment of adult patients with folate receptor alpha-positive, platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer who have received one to three prior systemic treatment regimens. When choosing between Vegzelma and Elahere, a patient's specific type of cancer, its molecular characteristics, previous treatments, and the overall treatment goals should be considered in consultation with a healthcare provider, as each medication has distinct mechanisms of action and is approved for different indications.

Difference between Vegzelma and Elahere

Metric Vegzelma (bevacizumab-adcd) Elahere (mirvetuximab soravtansine-gynx)
Generic name Bevacizumab-adcd Mirvetuximab soravtansine-gynx
Indications Metastatic colorectal cancer, non-small cell lung cancer, glioblastoma, metastatic renal cell carcinoma, cervical cancer, and ovarian cancer Ovarian cancer
Mechanism of action Angiogenesis inhibitor; monoclonal antibody that binds to and inhibits vascular endothelial growth factor A (VEGF-A) Antibody-drug conjugate; targets folate receptor-alpha (FRα) and delivers the cytotoxic agent DM4 to kill cancer cells
Brand names Vegzelma Elahere
Administrative route Intravenous infusion Intravenous infusion
Side effects Hypertension, proteinuria, hemorrhage, gastrointestinal perforation, impaired wound healing Diarrhea, fatigue, nausea, abdominal pain, anemia, neutropenia
Contraindications Hypersensitivity to bevacizumab or any component of the formulation; gastrointestinal perforation; recent surgery Hypersensitivity to mirvetuximab soravtansine or any component of the formulation
Drug class Monoclonal antibody, angiogenesis inhibitor Antibody-drug conjugate
Manufacturer Celltrion ImmunoGen, Inc.

Efficacy

Vegzelma (bevacizumab-adcd) for Gynecological Cancers

Vegzelma (bevacizumab-adcd) is a biosimilar to the original bevacizumab product, which is a monoclonal antibody designed to inhibit vascular endothelial growth factor (VEGF). By targeting VEGF, Vegzelma helps to prevent the growth of blood vessels that supply tumors with oxygen and nutrients, which is essential for their growth and survival. The efficacy of bevacizumab in treating gynecological cancers, particularly ovarian cancer, has been established through clinical trials. It has been shown to prolong progression-free survival when used in combination with standard chemotherapy in patients with advanced epithelial ovarian, fallopian tube, or primary peritoneal cancer.

While Vegzelma itself may not have been directly studied in gynecological cancers, as a biosimilar, it is expected to have no clinically meaningful differences in terms of safety, purity, and potency in comparison to the reference product. Therefore, the efficacy outcomes observed with the original bevacizumab are likely to be indicative of Vegzelma's potential benefits in treating gynecological cancers when used as part of a combination regimen.

Elahere (mirvetuximab soravtansine-gynx) for Gynecological Cancers

Elahere (mirvetuximab soravtansine-gynx) is an antibody-drug conjugate targeting the folate receptor alpha (FRα), which is frequently overexpressed in ovarian and other types of gynecological cancers. By specifically binding to cells that overexpress FRα, Elahere delivers a potent cytotoxic agent directly to the cancer cells. This targeted approach helps to minimize the impact on normal, healthy cells and allows for the delivery of higher doses of the cytotoxic agent to the tumor site.

The efficacy of Elahere in treating gynecological cancers has been evaluated in clinical trials. In particular, studies have focused on its use in patients with platinum-resistant ovarian cancer, which is a challenging condition to treat due to the cancer's resistance to standard chemotherapy. Results from these trials have shown promise, with some patients experiencing significant shrinkage of their tumors. The response rates and duration of response observed in these studies suggest that Elahere could offer a new therapeutic option for patients with FRα-positive gynecological cancers, particularly those with limited treatment options due to resistance to other therapies.

Regulatory Agency Approvals

Vegzelma
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
Elahere
  • Food and Drug Administration (FDA), USA

Access Vegzelma or Elahere today

If Vegzelma or Elahere are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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