Claims for Patent: 7,682,612

Summary for Patent: 7,682,612

Title:	Treatment of hematologic malignancies associated with circulating tumor cells using chimeric anti-CD20 antibody
Abstract:	Chronic Lymphocytic Leukemia (CLL) may be treated with antibodies directed against the CD20 antigen.
Inventor(s):	White; Christine A. (Rancho Santa Fe, CA), Grillo-Lopez; Antonio J. (Rancho Santa Fe, CA), Curd; John G. (Hillsborough, CA), Desmond-Hellmann; Susan (Alamo, CA)
Assignee:	Biogen Idec Inc. (Cambridge, MA) Genentech, Inc. (South San Francisco, CA)
Application Number:	09/436,347
Patent Litigation and PTAB cases:	See patent lawsuits and PTAB cases for patent 7,682,612
Patent Claims:	1. A method of treating chronic lymphocytic leukemia in a human patient, comprising administering an anti-CD20 antibody to the patient in an amount effective to treat the chronic lymphocytic leukemia, wherein the method does not include treatment with a radiolabeled anti-CD20 antibody. 2. A method according to claim 1, wherein the anti-CD20 antibody is administered to the patient at a dosage of about 0.001 to about 30 mg/kg. 3. A method according to claim 1, wherein the anti-CD20 antibody is administered to the patient at a dosage of about 0.01 to about 25 mg/kg. 4. A method according to claim 1, wherein the anti-CD20 antibody is administered to the patient at a dosage of about 0.1 to about 20 mg/kg. 5. A method according to claim 1, wherein the anti-CD20 antibody is administered to the patient at a dosage of about 375 mg/m.sup.2. 6. A method of treating chronic lymphocytic leukemia in a human patient, comprising administering an anti-CD20 antibody to the patient in an amount effective to treat the chronic lymphocytic leukemia, wherein the anti-CD20 antibody is administered to the patient at a dosage of about 500 to about 1500 mg/m.sup.2, wherein the method does not include treatment with a radiolabeled anti-CD20 antibody. 7. A method according to claim 6, wherein the anti-CD20 antibody is administered to the patient at a dosage of about 500 mg/m.sup.2. 8. A method according to claim 1 or 6, wherein the patient has relapsed following previous treatment for the chronic lymphocytic leukemia. 9. A method according to claim 1 or 6, wherein the patient is refractory to a treatment previously administered for the chronic lymphocytic leukemia. 10. A method according to claim 9, wherein the patient is refractory to fludarabine. 11. A method according to claim 1 or 6, wherein the anti-CD20 antibody is a chimeric antibody. 12. A method according to claim 11, wherein the anti-CD20 antibody is rituximab. 13. A method according to claim 1 or 6, wherein the anti-CD20 antibody is a humanized antibody. 14. A method according to claim 1 or 6, wherein the anti-CD20 antibody is a human antibody. 15. A method according to claim 1 or 6, wherein the anti-CD20 antibody comprises a CD20-binding fragment of a chimeric, humanized, or human antibody. 16. A method according to claim 1 or 6, wherein the anti-CD20 antibody is administered to the patient repeatedly. 17. A method according to claim 16, wherein the anti-CD20 antibody is administered to the patient weekly. 18. A method according to claim 16, wherein the anti-CD20 antibody is administered to the patient weekly for about 2 to 10 weeks. 19. A method according to claim 16, wherein the anti-CD20 antibody is administered to the patient biweekly. 20. A method according to claim 16, wherein the anti-CD20 antibody is administered to the patient monthly. 21. A method according to claim 1 or 6, wherein the anti-CD20 antibody is administered to the patient parenterally. 22. A method according to claim 21, wherein the anti-CD20 antibody is administered to the patient by intravenous infusion. 23. A method of treating chronic lymphocytic leukemia in a human patient, comprising administering an anti-CD20 antibody to the patient in an amount effective to treat the chronic lymphocytic leukemia, wherein the anti-CD20 antibody therapy is combined with chemotherapy, wherein the method does not include treatment with a radiolabeled anti-CD20 antibody. 24. A method according to claim 23, wherein the anti-CD20 antibody is administered to the patient at a dosage of about 0.001 to about 30 mg/kg. 25. A method according to claim 23, wherein the anti-CD20 antibody is administered to the patient at a dosage of about 0.01 to about 25 mg/kg. 26. A method according to claim 23, wherein the anti-CD20 antibody is administered to the patient at a dosage of about 0.1 to about 20 mg/kg. 27. A method according to claim 23, wherein the anti-CD20 antibody is administered to the patient at a dosage of about 375 mg/m.sup.2. 28. A method of treating chronic lymphocytic leukemia in a human patient, comprising administering an anti-CD20 antibody to the patient in an amount effective to treat the chronic lymphocytic leukemia, wherein the anti-CD20 antibody is administered to the patient at a dosage of about 500 to about 1500 mg/m.sup.2, wherein the anti-CD20 antibody therapy is combined with chemotherapy, and wherein the method does not include treatment with a radiolabeled anti-CD20 antibody. 29. A method according to claim 28, wherein the anti-CD20 antibody is administered to the patient at a dosage of about 500 mg/m.sup.2. 30. A method according to claim 23 or 28, wherein the patient has relapsed following previous treatment for the chronic lymphocytic leukemia. 31. A method according to claim 23 or 28, wherein the patient is refractory to a treatment previously administered for the chronic lymphocytic leukemia. 32. A method according to claim 31, wherein the patient is refractory to fludarabine. 33. A method according to claim 23 or 28, wherein the anti-CD20 antibody is a chimeric antibody. 34. A method according to claim 33, wherein the anti-CD20 antibody is rituximab. 35. A method according to claim 23 or 28, wherein the anti-CD20 antibody is a humanized antibody. 36. A method according to claim 23 or 28, wherein the anti-CD20 antibody is a human antibody. 37. A method according to claim 23 or 28, wherein the anti-CD20 antibody comprises a CD20-binding fragment of a chimeric, humanized, or human antibody. 38. A method according to claim 23 or 28, wherein the anti-CD20 antibody is administered to the patient repeatedly. 39. A method according to claim 38, wherein the anti-CD20 antibody is administered to the patient weekly. 40. A method according to claim 38, wherein the anti-CD20 antibody is administered to the patient weekly for about 2 to 10 weeks. 41. A method according to claim 38, wherein the anti-CD20 antibody is administered to the patient biweekly. 42. A method according to claim 38, wherein the anti-CD20 antibody is administered to the patient monthly. 43. A method according to claim 23 or 28, wherein the anti-CD20 antibody is administered to the patient parenterally. 44. A method according to claim 43, wherein the anti-CD20 antibody is administered to the patient by intravenous infusion. 45. A method according to claim 23 or 28, wherein the anti-CD20 antibody therapy and the chemotherapy are administered to the patient concurrently. 46. A method according to claim 23 or 28, wherein the chemotherapy comprises chlorambucil. 47. A method according to claim 23 or 28, wherein the chemotherapy comprises cyclophosphamide. 48. A method according to claim 47, wherein the chemotherapy comprises cyclophosphamide, vincristine, and prednisone (COP). 49. A method according to claim 47, wherein the chemotherapy comprises cyclophosphamide, vincristine, prednisone, and doxorubicin (CHOP). 50. A method according to claim 23 or 28, wherein the chemotherapy comprises vincristine. 51. A method according to claim 23 or 28, wherein the chemotherapy comprises prednisone. 52. A method according to claim 23 or 28, wherein the chemotherapy comprises doxorubicin. 53. A method according to claim 23 or 28, wherein the chemotherapy comprises fludarabine. 54. A method according to claim 23 or 28, wherein the chemotherapy comprises methotrexate. 55. A method according to claim 23 or 28, wherein the chemotherapy comprises cisplatin. 56. A method according to claim 23 or 28, wherein the chemotherapy comprises toremifene. 57. A method according to claim 23 or 28, wherein the chemotherapy comprises tamoxifen. 58. A method of treating chronic lymphocytic leukemia in a human patient, comprising administering an anti-CD20 antibody to the patient in an amount effective to treat the chronic lymphocytic leukemia, wherein the patient is refractory to fludarabine previously administered for the chronic lymphocytic leukemia, and wherein the method does not include treatment with a radiolabeled anti-CD20 antibody. 59. A method according to claim 6, 28, or 58, wherein radiation is not used in conjunction with the anti-CD20 antibody. 60. A method of treating chronic lymphocytic leukemia in a human patient, comprising administering a therapeutic non-radiolabeled anti-CD20 antibody to the patient in an amount effective to treat the chronic lymphocytic leukemia, wherein radiation is not used in conjunction with said anti-CD20 antibody.

Details for Patent 7,682,612

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Genentech, Inc.	RITUXAN	rituximab	Injection	103705	11/26/1997		2018-11-09
Idec Pharmaceuticals Corp.	RITUXAN	rituximab	Injection	103737	02/19/2002		2018-11-09
Genentech, Inc.	RITUXAN HYCELA	rituximab and hyaluronidase human	Injection	761064	06/22/2017		2018-11-09