Elapegademase
Revcovi (elapegademase) is an enzyme pharmaceutical. Elapegademase was first approved as Revcovi on 2018-10-05.
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Commercial
Therapeutic Areas
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Trade Name
FDA
EMA
Revcovi
Drug Products
FDA
EMA
Reference product - 351(a)
Reference product - 351(a)
Interchangeable product - 351(k)
Interchangeable product - 351(k)
Biosimilar product - 351(k)
Biosimilar product - 351(k)
Elapegademase
Tradename | Proper name | Company | Number | Date | Products |
|---|---|---|---|---|---|
| Revcovi | elapegademase-lvlr | Chiesi Farmaceutici | N-761092 RX | 2018-10-05 | 1 products |
Labels
FDA
EMA
Brand Name | Status | Last Update |
|---|---|---|
| revcovi | Biologic Licensing Application | 2022-08-31 |
Indications
FDA
EMA
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Agency Specific
FDA
EMA
Expiration | Code | ||
|---|---|---|---|
elapegademase, Revcovi, Chiesi USA, Inc. | |||
| 2025-10-05 | Orphan excl. | ||
Patent Expiration
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HCPCS
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Clinical
Clinical Trials
2 clinical trials
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Indications Phases 4
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Indications Phases 3
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Indications Phases 2
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Indications Phases 1
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Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Severe combined immunodeficiency | D016511 | — | D81.0 | — | — | — | — | 1 | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
| Drug common name | Elapegademase |
| INN | elapegademase |
| Description | Elapegademase, sold under the brand name Revcovi, is a medication for the treatment of the rare disease adenosine deaminase deficiency-SCID in children and adults.
|
| Classification | Enzyme |
| Drug class | enzymes; PEGylated compounds, covalent attachment of macrogol (polyethylene glycol) polymer |
| Image (chem structure or protein) |  |
| Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
| PDB | — |
| CAS-ID | — |
| RxCUI | — |
| ChEMBL ID | CHEMBL3990026 |
| ChEBI ID | — |
| PubChem CID | — |
| DrugBank | DB14712 |
| UNII ID | 9R3D3Y0UHS (ChemIDplus, GSRS) |
Target
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Additional graphs summarizing 43 documents
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Safety
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263 adverse events reported
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