Mirvetuximab soravtansine, marketed under the brand name Elahere, is approved by the FDA for the treatment of adults with ovarian cancer, fallopian tube cancer, or primary peritoneal cancer. It is specifically used for patients who no longer respond to platinum-based chemotherapy and have received one to three prior types of chemotherapy. The FDA approved Mirvetuximab soravtansine (Elahere) on November 14, 2022.
Mirvetuximab soravtansine is administered intravenously and is typically given every three weeks as an infusion. The exact number of treatment cycles will be determined by your doctor. It may also be used for other purposes not listed in the medication guide.
Patients should be aware of the potential side effects, which can range from mild to serious. Some common side effects include:
More serious side effects requiring immediate medical attention include:
Mirvetuximab soravtansine can interact with other drugs, potentially altering its effectiveness or increasing the risk of side effects. Some known drug interactions include:
It is crucial to inform your healthcare provider about all the medications you are currently taking, including over-the-counter drugs and supplements, to avoid harmful interactions.
Mirvetuximab soravtansine (Elahere) is FDA approved for treating certain types of cancers in adults who are no longer responding to platinum-based chemotherapy. It is important for patients to be aware of potential side effects and interactions with other medications, and to work closely with their healthcare provider to ensure safe and effective treatment.
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