> Trialight public data. Index of pages: https://trialight.com/llms.txt
> Web page: https://trialight.com/data/asset/ensitrelvir-82b61684-fc6a-45cb-a8be-1d5ca6f70f95
> Record changed: 2026-10-13

# Ensitrelvir

Highest phase reached

Phase 3

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL5183847)

Drug type

Small molecule

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL5183847)

## Development status

**Listing at source**

Listed

**Highest phase reached**

Phase 3

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL5183847)

## Names and chemistry

**Drug type**

Small molecule

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL5183847)

**Drug name**

Ensitrelvir

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL5183847)

**Molecular weight**

531.89

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL5183847)

**Structure (SMILES)**

Cn1cnc(Cn2c(=O)\[nH\]/c(=N\\c3cc4cn(C)nc4cc3Cl)n(Cc3cc(F)c(F)cc3F)c2=O)n1

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL5183847)

### Other names (13)

- ensitrelvir
- Ensitrelvir
- Ensitrelvir \[INN\]
- Ensitrelvir \[MI\]
- Ensitrelvir \[USAN\]
- Ensitrelvir \[WHO-DD\]
- ensitrelvir inn
- ensitrelvir mi
- ensitrelvir usan
- ensitrelvir who dd
- s 217622
- S-217622
- Shionogi Protease Inhibitor (S-217622)

## Identifiers

**ATC classification codes**

- J05AE16

Sources for recorded values

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL5183847)

**CAS registry numbers**

- 2647530-73-0

**ChEMBL ID**

CHEMBL5183847

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL5183847)

**InChIKey**

QMPBBNUOBOFBFS-UHFFFAOYSA-N

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL5183847)

**PubChem compound IDs**

- 162533924

**RxNorm IDs (RxCUI)**

- 2745988

**FDA ingredient codes (UNII)**

- PX665RAA3H

## Regulatory information

### European Union

**Status**

opinion

**Status date**

23 Jun 2026

**Approved indications**

Treatment of coronavirus disease 2019 (COVID-19).

**Product number**

EMEA/H/C/006063

**Authorisation holder**

Shionogi B.V.

**Priority medicines scheme**

No

**Generic**

No

**Biosimilar**

No

**Generic medicines**

0

**Biosimilar medicines**

0

**Advanced therapy**

No

**Conditional approval**

No

**Additional monitoring**

No

**Accelerated assessment**

No

**Exceptional circumstances**

No

#### Therapeutic areas

- COVID-19 virus infection

European medicines record

Source: [www.ema.europa.eu](https://www.ema.europa.eu/en/medicines/human/EPAR/zokovea)

### Other regulatory facts

**First in class**

No

**Orphan designation**

No

## Pharmacology

### Drug classification

**Pharmacology name**

ensitrelvir

**Type**

Synthetic organic

**Drug name stem**

\-vir

**Approval recorded by Guide to Pharmacology**

Yes

### Investigated indications (6)

- **Condition**  
Severe Acute Respiratory Syndrome

**Highest recorded phase**  
3

**Condition identifier**  
EFO:0000694

**Subject identifier**  
D045169
- **Condition**  
Virus Diseases

**Highest recorded phase**  
3

**Condition identifier**  
EFO:0000763

**Subject identifier**  
D014777
- **Condition**  
Liver Diseases

**Highest recorded phase**  
1

**Condition identifier**  
EFO:0001421

**Subject identifier**  
D008107
- **Condition**  
Kidney Diseases

**Highest recorded phase**  
1

**Condition identifier**  
EFO:0003086

**Subject identifier**  
D007674
- **Condition**  
COVID-19

**Highest recorded phase**  
1

**Condition identifier**  
MONDO:0100096

**Subject identifier**  
D000086382
- **Condition**  
Severe Acute Respiratory Syndrome

**Highest recorded phase**  
3

**Condition identifier**  
MONDO:0100096

**Subject identifier**  
D045169

### Open Targets indications (6)

- **Condition identifier**  
EFO\_0000694

**Highest recorded phase**  
3
- **Condition identifier**  
EFO\_0000763
- **Condition identifier**  
EFO\_0001421

**Highest recorded phase**  
1
- **Condition identifier**  
EFO\_0003086

**Highest recorded phase**  
1
- **Condition identifier**  
MONDO\_0005108

**Highest recorded phase**  
4
- **Condition identifier**  
MONDO\_0100096

**Highest recorded phase**  
3

### Trial references (6)

- NCT05041907  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05041907)
- NCT05605093  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05605093)
- NCT05897541  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05897541)
- NCT05305547  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05305547)
- NCT05363215  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05363215)
- NCT05409911  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05409911)

## Chemical properties

**Hydrogen bond acceptors**

10

**Hydrogen bond donors**

1

**Polar surface area**

120.68

**Calculated partition coefficient (ALogP)**

1.75

**Calculated partition coefficient (XLogP)**

2.5

**Prodrug**

No

**Chirality**

Achiral

**Inorganic**

No

**Rule-of-five violations**

1

**Rotatable bonds**

5

**Heavy atoms**

37

**Molecular formula**

C22H17ClF3N9O2

**Monoisotopic mass**

531.1145830

**Natural product**

No

## National Drug Codes

- 59630-711

## Evidence counts

**Recorded assays**

102

**Active assays**

36

### Active assay types

- Confirmatory

## Biological measurements

### Observed measurements

#### Oral bioavailability

**Median**

96.7

**Mean**

96.7

**Minimum**

96.7

**Maximum**

96.7

**Unit**

%

**Assays**

1

**Standard deviation**

0

**Summary method**

median

**Censored results excluded**

0

**Other units excluded**

0

**Unknown units excluded**

0

#### Measurement types

- F

## Related records

### Trials (8)

- A Drug-Drug Interaction Study of S-217622 With Combined Oral Contraceptives in Healthy Adult Female Participants
- A Study to Assess S-217622 in Participants With Mild and Moderate Hepatic Impairment and Healthy Control Participants
- A Study to Assess S-217622 in Participants With Renal Impairment and Healthy Participants
- [A Study to Compare S-217622 With Placebo in Non-Hospitalized Participants With COVID-19](https://trialight.com/data/trial/a-study-to-compare-s-217622-with-placebo-in-non-hospitalized-a3b237fd-1afb-42a0-83c6-6f74c3b57617.md)
- Ensitrelvir for Viral Persistence and Inflammation in People Experiencing Long COVID
- Finding Treatments for COVID-19: A Trial of Antiviral Pharmacodynamics in Early Symptomatic COVID-19 (PLATCOV)
- [Phase 3 Study of S-217622 in Prevention of Symptomatic SARS-CoV-2 Infection](https://trialight.com/data/trial/phase-3-study-of-s-217622-in-prevention-of-symptomatic-sars-28beaa7d-4f42-4bb9-a830-2217cf7d6367.md)
- Strategies and Treatments for Respiratory Infections & Viral Emergencies (STRIVE): Shionogi Protease Inhibitor (Ensitrelvir)

### In development for (5)

- [COVID-19](https://trialight.com/data/condition/covid-19-13f0ebf3-c291-557d-bdef-93563d077103.md) Phase 3
- [Kidney disorder](https://trialight.com/data/condition/kidney-disorder-e50371fe-f1a7-53fe-9cfb-9d6da9130e3c.md) Phase 1
- [Liver disorder](https://trialight.com/data/condition/liver-disorder-8388d30a-2581-5015-9ddf-adc5f6a331d7.md) Phase 1
- [Severe acute respiratory syndrome](https://trialight.com/data/condition/severe-acute-respiratory-syndrome-7654d02a-f750-52a0-bec2-afe3b4b3c224.md) Phase 3
- [Viral infectious disease](https://trialight.com/data/condition/viral-infectious-disease-43db42a3-adad-5b9d-b74c-f17df0674c21.md) Phase 3

---

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