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Drug ReportsVUPANORSEN
VUPANORSEN
Vupanorsen is an oligonucleotide 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
7 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
Familial partial lipodystrophyD05249611
Type 2 diabetes mellitusD003924EFO_0001360E1111
Non-alcoholic fatty liver diseaseD065626EFO_0003095K75.8111
HypertriglyceridemiaD015228EFO_000421111
Hyperlipoproteinemia type vD006954Orphanet_70470E78.311
Hyperlipoproteinemia type iD008072Orphanet_411E78.311
HyperlipidemiasD006949HP_0003077E78.511
DyslipidemiasD050171HP_000311911
HyperlipoproteinemiasD006951HP_001098011
Hyperlipoproteinemia type iiD006938EFO_0004911E78.0011
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Healthy volunteers/patients22
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameVUPANORSEN
INNvupanorsen
Description
Vupanorsen is an oligonucleotide pharmaceutical. It is currently being investigated in clinical studies.
Classification
Oligonucleotide
Drug classantisense oligonucleotides
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Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID
RxCUI
ChEMBL IDCHEMBL4298197
ChEBI ID
PubChem CID
DrugBank
UNII IDA7YG62NHZ6 (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
Revenue by drug
$
£
Vupanorsen Ionis Pharmaceuticals
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Tabular view
Estimated US medical usage
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 157 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
0 adverse events reported
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