Tiragolumab
| Monoclonal antibody | |
|---|---|
| Type | ? |
| Clinical data | |
| Other names | RG6058, MTIG7192A |
| Routes of administration | Intravenous |
| Drug class | Immune checkpoint inhibitor |
| Identifiers | |
| CAS Number | |
| UNII | |
| KEGG | |
| ChEBI | |
| Chemical and physical data | |
| Formula | C6620H10206N1742O2074S40 |
| Molar mass | 148664.99 g·mol−1 |
Tiragolumab (development names RG6058 and MTIG7192A) is a humanized monoclonal antibody that functions as an immune checkpoint inhibitor by targeting the T-cell immunoreceptor with Ig and ITIM domains (TIGIT) pathway. Developed by Genentech and Roche, the drug is designed to enhance anti-tumor immune responses when used in combination with other immunotherapy agents, particularly atezolizumab (Tecentriq).
In January 2021, tiragolumab received breakthrough therapy designation from the U.S. Food and Drug Administration (FDA) for use in combination with atezolizumab in the treatment of patients with PD-L1-high metastatic non-small-cell lung cancer (NSCLC) who do not harbor EGFR mutations or ALK rearrangements.