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Elahere

Mirvetuximab Soravtansine-Gynx
Anticancer
Injection Injectable

Platinum-resistant ovarian cancer has poor outcomes and few targeted options, while folate receptor alpha is overexpressed in most cases. Elahere (mirvetuximab soravtansine) turned that into a treatment.

It delivers the maytansinoid DM4 into tumor cells to disrupt microtubules, making it the first folate receptor alpha-directed antibody-drug conjugate approved. The intravenous therapy treats FR-alpha-positive, platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer after prior systemic therapy.

Elahere’s accelerated approval converted to full approval in 2024 on confirmatory MIRASOL survival data, and companion FR-alpha testing shapes eligibility. Its ocular toxicity requires ophthalmic monitoring, and the asset was central to AbbVie’s acquisition of ImmunoGen.

Approval Date
14-Nov-22
Data Exclusivity Expiry
14-Nov-26
Market Exclusivity Expiry
14-Nov-34
Commercial snapshot

Market performance & projections

Revenue ($M)
690
CAGR (%)
22.76%
Projected sales, 2026–2032 ($M)
Analyst projection, $M per year
2026
914
2027
1,121
2028
1,373
2029
1,567
2030
1,753
2031
1,929
2032
2,099
Molecule profile

Details & specifications

Molecule
Mirvetuximab Soravtansine-Gynx
Innovator
IMMUNOGEN, INC.
Dosage Form
Injection Injectable
Strength
100 mg/20 mL single-dose vial
Therapeutic Category
Anticancer
Usage
To treat patients with recurrent ovarian cancer that is resistant to platinum therapy
Good to know

Frequently asked questions

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