DEXELVUCITABINE
Dexelvucitabine is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
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Commercial
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Clinical
Clinical Trials
11 clinical trials
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Indications Phases 4
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Indications Phases 3
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Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Hiv infections | D015658 | EFO_0000764 | B20 | 2 | 7 | — | — | — | 8 |
| Acquired immunodeficiency syndrome | D000163 | EFO_0000765 | B20 | — | 3 | — | — | — | 3 |
| Hepatitis b | D006509 | — | — | — | 2 | — | — | 1 | 3 |
| Chronic hepatitis b | D019694 | EFO_0004239 | B18.1 | — | 2 | — | — | 1 | 3 |
| Hepatitis | D006505 | — | K75.9 | — | 2 | — | — | 1 | 3 |
| Hepatitis a | D006506 | EFO_0007305 | B15 | — | 2 | — | — | 1 | 3 |
| Infections | D007239 | EFO_0000544 | — | — | 2 | — | — | — | 2 |
| Chronic hepatitis | D006521 | — | K73.9 | — | 1 | — | — | 1 | 2 |
| Hiv | D006678 | — | O98.7 | — | 1 | — | — | — | 1 |
Indications Phases 1
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Indications Without Phase
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
| Drug common name | DEXELVUCITABINE |
| INN | dexelvucitabine |
| Description | Dexelvucitabine is a failed experimental agent for the management of human immunodeficiency virus infection. It is a cytidine nucleoside analog and nucleoside reverse transcriptase inhibitor. that inhibits HIV-1 replication in vitro. During phase II clinical trials there was some indication of a decreased mean viral load in patients with infected human immunodeficiency virus.
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| Classification | Small molecule |
| Drug class | nucleoside antiviral or antineoplastic agents, cytarabine or azarabine derivatives |
| Image (chem structure or protein) |  |
| Structure (InChI/SMILES or Protein Sequence) | Nc1nc(=O)n([C@H]2C=C[C@@H](CO)O2)cc1F |
Identifiers
| PDB | — |
| CAS-ID | 134379-77-4 |
| RxCUI | — |
| ChEMBL ID | CHEMBL109831 |
| ChEBI ID | — |
| PubChem CID | 64973 |
| DrugBank | — |
| UNII ID | KU8SPJ271W (ChemIDplus, GSRS) |
Target
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Financial
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Trends
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Safety
Black-box Warning
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Adverse Events
0 adverse events reported
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