Darvadstrocel
Alofisel (darvadstrocel) is a cell pharmaceutical. Darvadstrocel was first approved as Alofisel on 2018-03-23. It has been approved in Europe to treat rectal fistula.
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Commercial
Trade Name
FDA
EMA
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Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Labels
FDA
EMA
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Indications
FDA
EMA
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Agency Specific
FDA
EMA
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Patent Expiration
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HCPCS
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Clinical
Clinical Trials
10 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
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Crohn disease | D003424 | EFO_0000384 | K50 | 1 | 1 | 5 | 1 | 2 | 9 |
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 |
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Rectal fistula | D012003 | HP_0010447 | K60.3 | 1 | 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 | DARVADSTROCEL |
INN | darvadstrocel |
Description | Darvadstrocel, sold under the brand name Alofisel, is a medication used to treat complex perianal fistulas in adults with non-active/mildly active luminal Crohn's disease when fistulas have shown an inadequate response to at least one conventional or biologic therapy. It contains mesenchymal stem cells from fat tissue of adult donors.
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Classification | Cell |
Drug class | — |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
PDB | — |
CAS-ID | — |
RxCUI | — |
ChEMBL ID | CHEMBL4298180 |
ChEBI ID | — |
PubChem CID | — |
DrugBank | DB16581 |
UNII ID | 31W7R94KYT (ChemIDplus, GSRS) |
Target
Agency Approved
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Alternate
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Variants
Clinical Variant
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Financial
Alofisel - Takeda
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Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 193 documents
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Safety
Black-box Warning
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Adverse Events
Top Adverse Reactions
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310 adverse events reported
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