Atezolizumab/hyaluronidase
{{Short description|Combination medication}}
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| component1 = Atezolizumab
| class1 = Monoclonal antibody
| component2 = Hyaluronidase
| class2 = Endoglycosidase
| tradename = Tecentriq Hybreza
| Drugs.com = {{drugs.com|parent|Tecentriq-hybreza}}
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| DailyMedID = Atezolizumab and hyaluronidase
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| routes_of_administration = Subcutaneous
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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. It contains atezolizumab, a programmed death-ligand 1 (PD-L1) blocking monoclonal antibody; and hyaluronidase (human recombinant), an endoglycosidase. It is taken by subcutaneous injection.{{cite web | title=Tecentriq Hybreza- atezolizumab and hyaluronidase-tqjs injection | website=DailyMed | date=25 September 2024 | url=https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=a617b089-ce66-464b-987b-b45d029b4d6f | access-date=5 October 2024}}
The most common adverse reactions include fatigue, musculoskeletal pain, cough, dyspnea, and decreased appetite.
Atezolizumab/hyaluronidase was approved for medical use in the United States in September 2024.{{cite web | title=FDA approves atezolizumab and hyaluronidase-tqjs | website=U.S. Food and Drug Administration | date=12 September 2024 | url=https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-atezolizumab-and-hyaluronidase-tqjs-subcutaneous-injection | access-date=14 September 2024 | archive-date=14 September 2024 | archive-url=https://web.archive.org/web/20240914055712/https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-atezolizumab-and-hyaluronidase-tqjs-subcutaneous-injection | url-status=live }} {{PD-notice}}{{cite press release | title=FDA Approves Genentech's Tecentriq Hybreza, the First and Only Subcutaneous Anti-PD-(L)1 Cancer Immunotherapy | website=Genentech | date=12 September 2024 | url=https://www.gene.com/media/press-releases/15035/2024-09-12/fda-approves-genentechs-tecentriq-hybrez | access-date=14 September 2024 | archive-date=13 September 2024 | archive-url=https://web.archive.org/web/20240913041829/https://www.gene.com/media/press-releases/15035/2024-09-12/fda-approves-genentechs-tecentriq-hybrez | url-status=live }}{{cite press release | title=Halozyme Announces FDA Approval of Roche's Tecentriq Hybreza With Enhanze for Multiple Types of Cancer | publisher=Halozyme Therapeutics | via=PR Newswire | date=12 September 2024 | url=https://www.prnewswire.com/news-releases/halozyme-announces-fda-approval-of-roches-tecentriq-hybreza-with-enhanze-for-multiple-types-of-cancer-302247280.html | access-date=14 September 2024 | archive-date=13 September 2024 | archive-url=https://web.archive.org/web/20240913013612/https://www.prnewswire.com/news-releases/halozyme-announces-fda-approval-of-roches-tecentriq-hybreza-with-enhanze-for-multiple-types-of-cancer-302247280.html | url-status=live }}
Medical uses
History
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. A total of 371 participants were randomized (2:1) to receive subcutaneous atezolizumab and hyaluronidase or intravenous atezolizumab until disease progression or unacceptable toxicity.
References
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External links
- {{ClinicalTrialsGov|NCT03735121|A Study to Investigate Atezolizumab Subcutaneous in Patients With Previously Treated Locally Advanced or Metastatic Non-Small Cell Lung Cancer}}
{{Targeted cancer therapeutic agents}}
{{Monoclonals for tumors}}
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{{DEFAULTSORT:Atezolizumab Hyaluronidase}}
Category:Drugs developed by Genentech
Category:Drugs developed by Hoffmann-La Roche
Category:Monoclonal antibodies for tumors
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