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Drug ReportsELVUCITABINE
ELVUCITABINE
Elvucitabine is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
Max
Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
No data
Clinical
Clinical Trials
11 clinical trials
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Indications Phases 4
No data
Indications Phases 3
No data
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Hiv infectionsD015658EFO_0000764B2015———5
Hepatitis bD006509———2——13
Chronic hepatitis bD019694EFO_0004239B18.1—2——13
HepatitisD006505—K75.9—2——13
Hepatitis aD006506EFO_0007305B15—2——13
InfectionsD007239EFO_0000544——2———2
Acquired immunodeficiency syndromeD000163EFO_0000765B20—2———2
Chronic hepatitisD006521—K73.9—1——12
Indications Phases 1
No data
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameELVUCITABINE
INNelvucitabine
Description
Elvucitabine is an experimental nucleoside reverse transcriptase inhibitor (NRTI), developed by Achillion Pharmaceuticals, Inc. for the treatment of HIV infection.
Classification
Small molecule
Drug classnucleoside antiviral or antineoplastic agents, cytarabine or azarabine derivatives
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Structure (InChI/SMILES or Protein Sequence)
Nc1nc(=O)n([C@@H]2C=C[C@H](CO)O2)cc1F
Identifiers
PDB—
CAS-ID181785-84-2
RxCUI—
ChEMBL IDCHEMBL38700
ChEBI ID—
PubChem CID469717
DrugBank—
UNII IDM09BUF90C0 (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 55 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
0 adverse events reported
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