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Rylaze

Asparaginase Erwinia Chrysanthemi (Recombinant)-Rywn
Anticancer
Intramuscular Injectable

Asparaginase is essential to modern leukemia regimens, but hypersensitivity to E. coli-derived products forces a switch, and supply of the Erwinia alternative had been unreliable. Rylaze addressed both problems.

It depletes asparagine, an amino acid leukemia cells cannot synthesize but depend on to survive. Approved as a component of a chemotherapy regimen, it serves patients 1 month and older with acute lymphoblastic leukemia or lymphoblastic lymphoma who are allergic to E. coli-derived asparaginase.

As a recombinant product, Rylaze resolved the supply constraints that plagued the earlier Erwinia-derived enzyme, and it later added intravenous dosing alongside intramuscular administration. It holds orphan designation and remains the default option for hypersensitive patients.

Approval Date
30-Jun-21
Data Exclusivity Expiry
30-Jun-25
Market Exclusivity Expiry
30-Jun-33
Commercial snapshot

Market performance & projections

Revenue ($M)
403
CAGR (%)
4.58%
Projected sales, 2026–2032 ($M)
Analyst projection, $M per year
2026
429
2027
448
2028
464
2029
482
2030
501
2031
516
2032
531
Molecule profile

Details & specifications

Molecule
Asparaginase Erwinia Chrysanthemi (Recombinant)-Rywn
Innovator
JAZZ PHARMACEUTICALS, INC.
Dosage Form
Intramuscular Injectable
Strength
10 mg/0.5 mL
Therapeutic Category
Anticancer
Usage
To treat acute lymphoblastic leukemia and lymphoblastic lymphoma in patients who are allergic to E. coli-derived asparaginase products, as a component of a chemotherapy regimen
Good to know

Frequently asked questions

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