Anti-tissue factor antibody-drug conjugates and their use in the treatment of cancer
AssigneeGenmab A/S
InventorReshma A. RANGWALA
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Abstract
The invention provides methods and compositions for treating cancer, such as advanced cervical cancer, in a subject, such as by the administration of antibody-drug conjugates that bind to tissue factor (TF). The invention also provides articles of manufacture and compositions comprising said antibody drug-conjugates that bind to TF for use in treating cancer (e.g., advanced cervical cancer).
Claims93
A method of treating cervical cancer in a subject, the method comprising administering to the subject an antibody-drug conjugate that binds to tissue factor (TF), wherein the antibody-drug conjugate is tisotumab vedotin or a biosimilar thereof, and wherein the antibody-drug conjugate is administered at a dose of 2.0 mg/kg once every 3 weeks, wherein the subject has been previously treated with bevacizumab.
A method of treating cervical cancer in a subject, the method comprising administering to the subject an antibody-drug conjugate that binds to tissue factor (TF), wherein the antibody-drug conjugate is tisotumab vedotin or a biosimilar thereof, and wherein the antibody-drug conjugate is administered at a dose of 2.0 mg/kg once every 3 weeks, wherein the subject has not been previously treated with bevacizumab.
A method of treating cervical cancer in a subject, the method comprising administering to the subject an antibody-drug conjugate that binds to tissue factor (TF), wherein the antibody-drug conjugate is tisotumab vedotin or a biosimilar thereof, and wherein the antibody-drug conjugate is administered at a dose of 2.0 mg/kg once every 3 weeks, wherein the subject has an Eastern Cooperative Oncology Group (ECOG) score of 0.
A method of treating cervical cancer in a subject, the method comprising administering to the subject an antibody-drug conjugate that binds to tissue factor (TF), wherein the antibody-drug conjugate is tisotumab vedotin or a biosimilar thereof, and wherein the antibody-drug conjugate is administered at a dose of 2.0 mg/kg once every 3 weeks, wherein the subject has an ECOG score of 1.
A method of treating cervical cancer in a subject, the method comprising administering to the subject an antibody-drug conjugate that binds to tissue factor (TF), wherein the antibody-drug conjugate is tisotumab vedotin or a biosimilar thereof, and wherein the antibody-drug conjugate is administered at a dose of 2.0 mg/kg once every 3 weeks, wherein the subject is less than 65 years old.
A method of treating cervical cancer in a subject, the method comprising administering to the subject an antibody-drug conjugate that binds to tissue factor (TF), wherein the antibody-drug conjugate is tisotumab vedotin or a biosimilar thereof, and wherein the antibody-drug conjugate is administered at a dose of 2.0 mg/kg once every 3 weeks, wherein the objective response rate is between about 13% and about 35%, optionally, wherein the objective response rate is at least about 14%, about 19%, about 21%, 23.8%, about 24%, about 25%, about 26%, about 28%, about 30%, or about 33%.
A method of treating cervical cancer in a subject, the method comprising administering to the subject an antibody-drug conjugate that binds to tissue factor (TF), wherein the antibody-drug conjugate is tisotumab vedotin or a biosimilar thereof, and wherein the antibody-drug conjugate is administered at a dose of 2.0 mg/kg once every 3 weeks, wherein the subject exhibits progression-free survival of at least about 3 months after administration of the antibody-drug conjugate, optionally, wherein the subject exhibits progression-free survival of at least about 4 months, about 5 months, or about 6 months after administration of the antibody-drug conjugate.
A method of treating cervical cancer in a subject, the method comprising administering to the subject an antibody-drug conjugate that binds to tissue factor (TF), wherein the antibody-drug conjugate is tisotumab vedotin or a biosimilar thereof, and wherein the antibody-drug conjugate is administered at a dose of 2.0 mg/kg once every 3 weeks, wherein the subject exhibits overall survival of at least about 10 months after administration of the antibody-drug conjugate, optionally, wherein the subject exhibits overall survival of at least about 11 months, about 12 months, about 13 months, or 14 months after administration of the antibody-drug conjugate.
A method of treating cervical cancer in a subject, the method comprising administering to the subject an antibody-drug conjugate that binds to tissue factor (TF), wherein the antibody-drug conjugate is tisotumab vedotin or a biosimilar thereof, and wherein the antibody-drug conjugate is administered at a dose of 2.0 mg/kg once every 3 weeks, wherein the duration of response to the antibody-drug conjugate is at least about 6 months after administration of the antibody-drug conjugate, optionally, wherein the duration of response to the antibody-drug conjugate is at least about 7 months, about 8 months or about 10 months after administration of the antibody-drug conjugate.
A method of treating cervical cancer in a subject, the method comprising administering to the subject an antibody-drug conjugate that binds to tissue factor (TF), wherein the antibody-drug conjugate is tisotumab vedotin or a biosimilar thereof, and wherein the antibody-drug conjugate is administered at a dose of 2.0 mg/kg once every 3 weeks, wherein the time to response is less than about 6 months after administration of the antibody-drug conjugate, optionally, wherein the time to response is less than about 4 months, about 2 months, 1.4 months, or about 1.2 months after administration of the antibody-drug conjugate.
Dependencies are inferred from the claim text.