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Clinical
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Variants
Financial
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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
153 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Herpes zosterD006562EFO_0006510B0227223236
Healthy volunteers/patients112
Systemic sclerodermaD012595EFO_0000717M3422
Juvenile arthritisD001171EFO_1002007M0822
ArthritisD001168EFO_0005856M05-M1422
VasculitisD014657EFO_0006803M3122
Rheumatic diseasesD012216M79.022
Systemic vasculitisD05664722
Collagen diseasesD00309522
MyositisD009220EFO_0000783G72.4911
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Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Herpes simplexD006561B002520128
Human influenzaD007251EFO_0007328J11.1112
Respiratory syncytial virus infectionsD018357EFO_100141311
Respiratory syncytial virusesD01213611
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Stem cell transplantationD03358111
Bone marrow transplantationD01602611
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
LeukemiaD007938C9511
B-cell chronic lymphocytic leukemiaD015451C91.111
Waldenstrom macroglobulinemiaD008258C88.011
Lymphoid leukemiaD007945C9111
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
FrailtyD000073496R53.111
Yellow feverD015004A9511
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name
INN
Description
Classification
Unknown
Drug class
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Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID
RxCUI
ChEMBL ID
ChEBI ID
PubChem CID
DrugBank
UNII ID
Target
No data
Variants
No data
Financial
Revenue by drug
$
£
Zostavax Merck & Co
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Estimated US medical usage
No data
Trends
No data
Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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835 adverse events reported
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