Simnotrelvir/ritonavir
< Simnotrelvir
Chemical structures of simnotrelvir (top) and ritonavir (bottom) | |
| Combination of | |
|---|---|
| Simnotrelvir | SARS-CoV-2 3CLpro inhibitor |
| Ritonavir | Protease inhibitor |
| Clinical data | |
| Trade names | 先诺欣 (Xiannuoxin) |
| Pregnancy category |
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| Routes of administration | Oral |
| Legal status | |
| Legal status |
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| Clinical data | |
|---|---|
| Other names | SIM0417, SSD8432 |
| Routes of administration | Oral |
| Drug class | SARS-CoV-2 3CLpro inhibitor |
| Legal status | |
| Legal status |
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| Pharmacokinetic data | |
| Protein binding | 72.5% |
| Metabolism | hepatic (CYP3A) |
| Elimination half-life | 3.1 h; 4.1 h with ritonavir |
| Excretion | urine (55.4%), feces (36.7%) |
| Identifiers | |
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| PubChem CID | |
| Chemical and physical data | |
| Formula | C22H30F3N5O4S2 |
| Molar mass | 549.63 g·mol−1 |
| 3D model (JSmol) | |
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Simnotrelvir/ritonavir (trade name Xiannuoxin) is a pharmaceutical drug used for the treatment of COVID-19. Simnotrelvir/ritonavir is a combination drug of simnotrelvir, an inhibitor of SARS-CoV-2 3CLpro, and ritonavir, a CYP3A inhibitor.
It was developed by Simcere Pharmaceutical and conditionally approved in China by the National Medical Products Administration (NMPA) in January 2023. Results for the phase Ib trial are available. In a phase II/III trial, it reduced the duration of symptoms by a median of 36 hours compared to placebo.