US2023212311A1PendingUtilityA1

Fixed dosing of her antibodies

Assignee: GENENTECH INCPriority: Jan 21, 2005Filed: Jun 15, 2022Published: Jul 6, 2023
Est. expiryJan 21, 2025(expired)· nominal 20-yr term from priority
A61K 39/39558C07K 16/32A61K 39/3955A61K 31/337A61K 38/18A61J 1/065A61K 45/06Y10T428/13C07K 16/40A61K 31/7068C07K 16/22A61K 31/704A61K 2039/505A61K 39/395A61K 2039/545C07K 2317/24C07K 2317/56A61P 1/04A61P 11/00A61P 13/08A61P 15/00A61P 35/00A61P 35/04C07K 2317/94C07K 2317/76C07K 16/2863A61K 2039/54
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Claims

Abstract

The present invention concerns fixed dosing of HER antibodies, such as Pertuzumab.

Claims

exact text as granted — not AI-modified
1 - 36 . (canceled) 
     
     
         37 . A method of treating cancer in a human patient comprising administering at least one fixed dose of pertuzumab to the patient, wherein the fixed dose is selected from the group consisting of approximately 420 mg, approximately 525 mg, approximately 840 mg, and approximately 1050 mg of pertuzumab. 
     
     
         38 . The method of  claim 37  wherein a fixed dose of pertuzumab is administered to the patient approximately every 3 weeks. 
     
     
         39 . The method of  claim 37  wherein the cancer is selected from the group consisting of ovarian cancer, peritoneal cancer, fallopian tube cancer, metastatic breast cancer (MBC), non-small cell lung cancer (NSCLC), prostate cancer, and colorectal cancer. 
     
     
         40 . The method of  claim 37  wherein the fixed dose is selected from the group consisting of 420 mg, 525 mg, 840 mg, and 1050 mg of pertuzumab. 
     
     
         41 . An article of manufacture comprising a vial containing a fixed dose of a HER antibody, wherein the fixed dose is selected from the group consisting of approximately 420 mg, approximately 525 mg, approximately 840 mg, and approximately 1050 mg of the HER antibody. 
     
     
         42 . The article of manufacture of  claim 41  wherein the HER antibody is pertuzumab. 
     
     
         43 . The article of manufacture of  claim 41  wherein the fixed dose is selected from the group consisting of 420 mg, 525 mg, 840 mg, and 1050 mg of the HER antibody. 
     
     
         44 . The article of manufacture of  claim 41  further comprising a package insert instructing the user to administer the fixed dose to a cancer patient. 
     
     
         45 . The article of manufacture of  claim 44  wherein the cancer is selected from the group consisting of ovarian cancer, peritoneal cancer, fallopian tube cancer, metastatic breast cancer (MBC), non-small cell lung cancer (NSCLC), prostate cancer, and colorectal cancer. 
     
     
         46 . The article of manufacture of  claim 44  wherein the package insert further instructs the user to administer the fixed dose to a cancer patient whose cancer displays HER expression, amplification, or activation. 
     
     
         47 . The article of manufacture of  claim 41  comprising two vials, wherein a first vial contains a fixed dose of approximately 840 mg of pertuzumab, and a second vial contains a fixed dose of approximately 420 mg of pertuzumab. 
     
     
         48 . The article of manufacture of  claim 41  comprising two vials, wherein a first vial contains a fixed dose of approximately 1050 mg of pertuzumab, and a second vial contains a fixed dose of approximately 525 mg of pertuzumab.

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