| CPC A61K 47/6889 (2017.08) [A61K 31/475 (2013.01); A61K 31/573 (2013.01); A61K 31/655 (2013.01); A61K 31/675 (2013.01); A61K 31/704 (2013.01); A61K 39/39558 (2013.01); A61K 45/06 (2013.01); A61K 47/68031 (2023.08); A61K 47/6811 (2017.08); A61K 47/6817 (2017.08); A61K 47/6849 (2017.08); A61K 47/6851 (2017.08); A61P 35/00 (2018.01); A61P 35/02 (2018.01); C07K 16/2878 (2013.01); A61K 2039/505 (2013.01); A61K 2039/545 (2013.01); A61K 2039/55 (2013.01); C07K 2317/24 (2013.01); C07K 2317/90 (2013.01); C07K 2317/94 (2013.01)] | 14 Claims | 
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               1. A method of treating a hematological or lymphoid cancer in a non-adult human subject comprising administering to the subject brentuximab vedotin at a body surface area adjusted dose of 71.5 mg/m2, wherein the hematological or lymphoid cancer expresses CD30. 
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