Sotrovimab
drugOn this page
Also known as GSK-4182136GSK4182136Vir-7831VIR7831Xevudy
Summary
Sotrovimab (CHEMBL4650524) is an approved antibody (ATC J06BD05); indicated across 2 conditions including severe acute respiratory syndrome.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Antibody
- ATC class: J06BD05
- Indications: 2 conditions
- Clinical trials: 23
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL4650524 |
| Name | Sotrovimab |
| Type | Antibody |
| Max phase | 4 |
| ATC | J06BD05 |
Also known as: GSK-4182136, GSK4182136, Sotrovimab, Vir-7831, VIR-7831, VIR7831, Xevudy, SOTROVIMAB
Targets
Targets
Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).
| Gene | Target | Action | pAffinity | Cancer dependency | UniProt |
|---|---|---|---|---|---|
| CoV Spike glycoprotein | Binding |
Bioactivity
No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
2 indications (2 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| severe acute respiratory syndrome | 4 | MONDO:0005091 | MONDO:0100096 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 23.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE3 | 6 |
| PHASE2 | 5 |
| Not specified | 4 |
| PHASE1 | 3 |
| PHASE4 | 2 |
| PHASE2/PHASE3 | 2 |
| PHASE1/PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT04790786 | PHASE4 | TERMINATED | UPMC OPTIMISE-C19 Trial, a COVID-19 Study |
| NCT05305651 | PHASE4 | COMPLETED | Study to Monitor the Occurrence of Viral Variants in Patients With Compromised Immune Systems Being Treated for COVID-19 |
| NCT04381936 | PHASE3 | RECRUITING | Randomised Evaluation of COVID-19 Therapy |
| NCT04501978 | PHASE3 | COMPLETED | ACTIV-3: Therapeutics for Inpatients With COVID-19 |
| NCT04545060 | PHASE2/PHASE3 | COMPLETED | VIR-7831 for the Early Treatment of COVID-19 in Outpatients |
| NCT04870333 | PHASE2/PHASE3 | COMPLETED | PROphylaxis for paTiEnts at Risk of COVID-19 infecTion -V |
| NCT04913675 | PHASE3 | TERMINATED | Intramuscular and Intravenous VIR-7831 (Sotrovimab) for Mild/Moderate COVID-19. |
| NCT05205759 | PHASE3 | TERMINATED | Non-inferiority Trial on Monoclonal Antibodies in COVID-19 |
| NCT05321394 | PHASE3 | COMPLETED | Non-inferiority Trial on Treatments in Early COVID-19 |
| NCT05780281 | PHASE3 | COMPLETED | VIR-7831 for Inpatients With COVID-19 (An ACTIV-3/TICO Treatment Trial) |
| NCT04746183 | PHASE1/PHASE2 | RECRUITING | AGILE (Early Phase Platform Trial for COVID-19) |
| NCT05041907 | PHASE2 | RECRUITING | Finding Treatments for COVID-19: A Trial of Antiviral Pharmacodynamics in Early Symptomatic COVID-19 (PLATCOV) |
| NCT04634409 | PHASE2 | COMPLETED | A Study of Immune System Proteins in Participants With Mild to Moderate COVID-19 Illness |
| NCT04779879 | PHASE2 | COMPLETED | Safety, Tolerability and Pharmacokinetics of Second Generation VIR-7831 Material in Non-hospitalized Participants With Mild to Moderate COVID-19 |
| NCT05124210 | PHASE2 | TERMINATED | Pharmacokinetics, Pharmacodynamics, and Safety of Single-dose Sotrovimab in High-risk Pediatric Participants With Mild to Moderate COVID-19 |
| NCT05210101 | PHASE2 | COMPLETED | A Safety and Tolerability Study of Sotrovimab (VIR-7831) Prophylaxis Against COVID-19 in Immunocompromised Individuals |
| NCT04988152 | PHASE1 | COMPLETED | A Study to Investigate the PK, Safety, and Tolerability of Sotrovimab vs Placebo Administered IV or IM in Japanese and Caucasian Participants |
| NCT05135650 | PHASE1 | TERMINATED | Pharmacokinetics of Sotrovimab as Pre-exposure Prophylaxis for COVID-19 in Hematopoietic Stem Cell Transplant Recipients, COVIDMAB Study |
| NCT05280717 | PHASE1 | TERMINATED | Relative Bioavailability, Safety, and Tolerability of Single-dose Sotrovimab Injection in Adults (COSMIC) |
| NCT05195060 | Not specified | COMPLETED | TURN-COVID Biobank: The Dutch Cohort Study for the Evaluation of the Use of Neutralizing Monoclonal Antibodies and Other Antiviral Agents Against SARS-CoV-2 |
| NCT05235347 | Not specified | NO_LONGER_AVAILABLE | Sotrovimab Expanded Access Treatment Protocol (COVID-19) |
| NCT05268601 | Not specified | COMPLETED | COVID-19 and Disease Progression to the Severe Form: a Study on the Use of Monoclonal Antibodies Against SARS-CoV-2 |
| NCT05398718 | Not specified | UNKNOWN | Study on Sotrovimab and Its Impact on the Immune Response to COVID-19 Infection in Real-life in the UAE and Bahrain |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- Diseases: severe acute respiratory syndrome