Combination of | |
---|---|
Atezolizumab | Monoclonal antibody |
Hyaluronidase | Endoglycosidase |
Clinical data | |
Trade names | Tecentriq Hybreza |
AHFS/Drugs.com | Tecentriq-hybreza |
License data | |
Routes of administration | Subcutaneous |
ATC code |
|
Legal status | |
Legal status |
Atezolizumab/hyaluronidase, sold under the brand name Tecentriq Hybreza, is a fixed-dose combination medication used for the treatment of non-small cell lung cancer, small cell lung cancer, hepatocellular carcinoma, melanoma, and alveolar soft part sarcoma. [1] [2] It contains atezolizumab, a programmed death-ligand 1 (PD-L1) blocking monoclonal antibody; and hyaluronidase (human recombinant), an endoglycosidase. [1] It is taken by subcutaneous injection. [1]
The most common adverse reactions include fatigue, musculoskeletal pain, cough, dyspnea, and decreased appetite. [1] [2]
Atezolizumab/hyaluronidase was approved for medical use in the United States in September 2024. [1] [2] [3] [4]
Atezolizumab/hyaluronidase is a subcutaneous injection version of atezolizumab for all the adult indications as the intravenous formulation of atezolizumab including non-small cell lung cancer, small cell lung cancer, hepatocellular carcinoma, melanoma, and alveolar soft part sarcoma. [2]
The subcutaneous injection of atezolizumab and hyaluronidase was evaluated in IMscin001 (NCT03735121), an open-label, multi-center, international, randomized trial in adults with locally advanced or metastatic non-small cell lung cancer who were not previously exposed to cancer immunotherapy and who had disease progression following treatment with platinum-based chemotherapy. [2] A total of 371 participants were randomized (2:1) to receive subcutaneous atezolizumab and hyaluronidase or intravenous atezolizumab until disease progression or unacceptable toxicity. [2]