Bictegravir
ANTIINFECTIVES FOR SYSTEMIC USE
Also known as: bictegravir sodium, GS-9883, GS-9883-01
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Bictegravir is an onp drug catalogued in DrugCentral. It was first approved by the FDA in 2018. DrugCentral lists 3 molecular targets, including pol, Integrase and SLC22A2. Recorded indications include Human immunodeficiency virus infection.
- Approval status: onp (first approved 2018 by the FDA).
- Molecular targets: pol, Integrase and SLC22A2 (3 listed in DrugCentral).
- Indications: Human immunodeficiency virus infection.
- ATC code: J05AR20 (Antivirals for treatment of HIV infections, combinations).
- Molecular formula: C21H18F3N3O5; molecular weight 449.39 g/mol.
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (1)
- Human immunodeficiency virus infection
Mechanism & targets
Molecular targets (3)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Integrase | pol | inhibitor | IC50 8.12 |
| Integrase | — | unknown | IC50 8.12 |
| Solute carrier family 22 member 2 | SLC22A2 | unknown | IC50 6.31 |
Regulatory approvals (3)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2019-03-26 | PMDA | — | Gilead Sciences K.K. | Yes |
| 2018-06-21 | EMA | — | Gilead Sciences International Limited | |
| 2018-02-07 | FDA | — | GILEAD SCIENCES INC |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
J05AR20 | ANTIINFECTIVES FOR SYSTEMIC USE › ANTIVIRALS FOR SYSTEMIC USE › DIRECT ACTING ANTIVIRALS › Antivirals for treatment of HIV infections, combinations |
Reported adverse-event signals
Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.
| MedDRA term | LLR |
|---|---|
| Viral mutation identified | 82.5 |
| Pathogen resistance | 61.4 |
| Viral load increased | 58.8 |
| Drug resistance | 58.1 |
| Virologic failure | 48.4 |
Chemical structure
Full physicochemical, ADMET and 3D-structure analysis of Bictegravir is on its molecule page.
| Molecular formula | C21H18F3N3O5 |
|---|---|
| Molecular weight | 449.39 g/mol |
| CAS number | 1611493-60-7 |
| InChIKey | SOLUWJRYJLAZCX-LYOVBCGYSA-N |
| PubChem CID | 90311989 |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Bictegravir used for?
DrugCentral lists the following indications for Bictegravir: Human immunodeficiency virus infection.
How does Bictegravir work?
Its molecular targets in DrugCentral include pol (inhibitor), Integrase and SLC22A2.
When was Bictegravir first approved?
Bictegravir was first approved by the FDA in 2018.
What is the chemical formula of Bictegravir?
Bictegravir has the molecular formula C21H18F3N3O5 and a molecular weight of 449.39 g/mol.
Browse: all drugs starting with B · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 5274 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL3989866 — compound record and bioactivity
- PubChem CID 90311989 — chemical identifiers
- DrugBank DB11799 — drug record
- FDA UNII 8GB79LOJ07 — substance identity
- DailyMed: FDA labels for Bictegravir — current prescribing information (label search)
- UniProt O15244 (SLC22A2) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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