For intravenous use Initial U.S. Approval: 2022
As specified in the prescribing information, mosunetuzumab-axgb injection is indicated for the treatment of Lymphoma disease. As per highlights Of prescribing information mosunetuzumab-axgb injection is a bispecific CD20-directed CD3 T-cell engager indicated for the treatment of adult patients with relapsed or refractory follicular lymphoma after two or more lines of systemic therapy.
Facts about mosunetuzumab injection
Disease Indications: Lymphoma
Dosage Forms And Strengths:
• 1 mg/mL solution in a single-dose vial.
• 30 mg/30 mL (1 mg/mL) solution in a single-dose vial.
Manufacturer: Genentech, Inc
Medicine Approved By: European Medical Agency (EMA), Food and Drug Administration (FDA)
Lunsumio (mosunetuzumab-axgb) was approved by the EMA in June 20223 and the FDA in December 2022
- Full prescribing information [FDA]: [Click Here PDF]
- FDA grants accelerated approval to mosunetuzumab-axgb for relapsed or refractory follicular lymphoma
- Lunsumio (mosunetuzumab-axgb) EMA, June 2022
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Query For mosunetuzumab injection
Approved accessible "mosunetuzumab-axgb injection"
Mosunetuzumab, is a monoclonal antibody used for the treatment of follicular lymphoma. It bispecifically binds CD20 and CD3 to engage T-cells. It was developed by Genentech. Mosunetuzumab was approved for medical use in the European Union in June 2022, and in the United States in December 2022. The US Food and Drug Administration (FDA) considers it to be a first-in-class medication. Mosunetuzumab is indicated for the treatment of adults with relapsed or refractory follicular lymphoma after two or more lines of systemic therapy.
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