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Jemperli

Dostarlimab-Gxly
Anticancer
Injection Injectable

Checkpoint inhibitors reshaped gynecologic oncology, and mismatch repair status became one of the strongest predictors of response. Jemperli (dostarlimab) was developed around that biomarker.

By preventing PD-1 from restraining T cells, Jemperli allows the immune system to recognize and attack tumor cells. The intravenous antibody was first approved for adults with mismatch repair-deficient recurrent or advanced endometrial cancer that progressed on a platinum-containing regimen.

Jemperli still carries an ongoing accelerated approval for mismatch repair-deficient solid tumors and has since moved into earlier endometrial cancer treatment in combination with chemotherapy. As a biologic it faces no biosimilar competition, and its rectal cancer data have made it a closely watched asset.

Approval Date
22-Apr-21
Data Exclusivity Expiry
22-Apr-25
Market Exclusivity Expiry
22-Apr-33
Commercial snapshot

Market performance & projections

Revenue ($M)
1,135
CAGR (%)
15.49%
Projected sales, 2026–2032 ($M)
Analyst projection, $M per year
2026
1,423
2027
1,666
2028
1,863
2029
2,019
2030
2,152
2031
2,284
2032
2,415
Molecule profile

Details & specifications

Molecule
Dostarlimab-Gxly
Innovator
GLAXOSMITHKLINE LLC
Dosage Form
Injection Injectable
Strength
500 mg/10 mL
Therapeutic Category
Anticancer
Usage
To treat endometrial cancer
Good to know

Frequently asked questions

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