US2017037140A1PendingUtilityA1

Combination therapies for b-cell lymphomas comprising administration of anti-cd20 antibody

Assignee: BIOGEN INCPriority: Aug 11, 1998Filed: Oct 25, 2016Published: Feb 9, 2017
Est. expiryAug 11, 2018(expired)· nominal 20-yr term from priority
A61P 35/02A61P 43/00A61P 35/04A61P 35/00A61P 37/00A61K 31/704A61K 39/39558A61K 31/573C07K 16/2887C02F 1/003C07K 2317/77A61K 38/193A61K 51/1027A61K 38/2013A61K 31/675C02F 2307/02A61K 38/212A61K 39/39541C07K 2317/24A61K 31/475C07K 2317/56A61K 38/217C07K 16/3061A61K 51/1069A61K 2039/505A61K 2039/545A61K 39/395
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Claims

Abstract

New combined therapeutic regimens for treatment of B-cell lymphomas are disclosed which comprise, in particular, administration of anti-CD20 antibodies to patients having low-, intermediate- or high-grade non-Hodgkin's lymphomas.

Claims

exact text as granted — not AI-modified
1 . A method of treating B-cell lymphoma comprising administering to a patient a therapeutically effective amount of an anti-CD20 antibody subsequent to therapeutically effective chemotherapy. 
     
     
         2 . The method of  claim 1  wherein the chemotherapy is selected from the group consisting of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) and cyclophosphamide, vincristine, and prednisone (CVP). 
     
     
         3 . The method of  claim 1  wherein the anti-CD20 antibody comprises a chimeric antibody. 
     
     
         4 . The method of  claim 1  wherein the anti-CD20 antibody comprises rituximab. 
     
     
         5 . The method of  claim 1  wherein the anti-CD20 antibody comprises a light chain variable region comprising the amino acid sequence in SEQ ID NO: 1 and a heavy chain variable region comprising the amino acid sequence in SEQ ID NO: 2, and comprises human gamma 1 heavy-chain and kappa light-chain constant region amino acid sequences. 
     
     
         6 . The method of  claim 1  wherein the B-cell lymphoma comprises low grade or follicular non-Hodgkin's lymphoma (NHL). 
     
     
         7 . The method of  claim 6  wherein the anti-CD20 antibody is administered subsequent to the chemotherapy as a maintenance therapy. 
     
     
         8 . The method of  claim 7  wherein the maintenance therapy comprises administering 375 mg/m 2  anti-CD20 antibody for about 2 years. 
     
     
         9 . A method of treating low grade or follicular non-Hodgkin's lymphoma (NHL) comprising administering to a patient a therapeutically effective amount of rituximab subsequent to therapeutically effective chemotherapy selected from the group consisting of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) and cyclophosphamide, vincristine, and prednisone (CVP), wherein rituximab is administered as maintenance therapy comprising administering 375 mg/m 2  anti-CD20 antibody for about 2 years. 
     
     
         10 . A method of treating low grade or follicular non-Hodgkin's lymphoma (NHL) comprising administering to a patient a therapeutically effective amount of an anti-CD20 antibody subsequent to therapeutically effective chemotherapy selected from the group consisting of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) and cyclophosphamide, vincristine, and prednisone (CVP), wherein rituximab is administered as maintenance therapy comprising administering 375 mg/m 2  anti-CD20 antibody for about 2 years, and wherein the anti-CD20 antibody comprises a light chain variable region comprising the amino acid sequence in SEQ ID NO: 1 and a heavy chain variable region comprising the amino acid sequence in SEQ ID NO: 2, and comprises human gamma 1 heavy-chain and kappa light-chain constant region amino acid sequences. 
     
     
         11 . The method of  claim 9 , wherein the chemotherapy is CVP. 
     
     
         12 . The method of  claim 10 , wherein the chemotherapy is CVP.

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