tafasitamab-cxix for injection, for intravenous use Initial U.S. Approval: 2020
Monjuvi (tafasitamab-cxix) is a medication that is combined with lenalidomide for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL).
Facts about tafasitamab-cxix for injection
Medicine Approved By-Food and Drug Administration (FDA)
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)
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Query For tafasitamab-cxix for injection
Approved accessible "tafasitamab-cxix for injection"
tafasitamab-cxix)is approved by the U.S. Food and Drug Administration in combination with lenalidomide for the treatment of adult patients with relapsed or refractory DLBCL not otherwise specified, including DLBCL arising from low grade lymphoma, and who are not eligible for autologous stem cell transplant (ASCT).
Minjuvi is a cancer medicine used first in combination with another medicine called lenalidomide, and then on its own, to treat adults with diffuse large B-cell lymphoma (DLBCL) whose cancer has returned or has stopped responding to other treatments and who cannot have an autologous stem cell transplantation (a transplant where the stem cells are collected from the patients themselves).
DLBCL is rare, and Minjuvi was designated an ‘orphan medicine’ (a medicine used in rare diseases) on 15 January 2015. Further information on the orphan designation can be found here. Minjuvi contains the active substance tafasitamab.
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Monjuvi (tafasitamab-cxix) for injection for intravenous use Initial U.S. Approval: 2020
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