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Drug ReportsHuman cytomegalovirus immune globulin
Human cytomegalovirus immune globulin
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Events Timeline
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
21 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Cytomegalovirus infectionsD003586EFO_0001062B253432111
InfectionsD007239EFO_0000544233118
Communicable diseasesD003141233118
Chronic kidney failureD007676EFO_0003884N18.6112
CytomegalovirusD003587112
Organ transplantationD01637711
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Renal insufficiencyD051437N1911
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Hiv infectionsD015658EFO_0000764B20224
Cytomegalovirus retinitisD017726EFO_1001302123
RetinitisD012173H30.9123
Central nervous system diseasesD002493G96.9111
Nervous system diseasesD009422G00-G99111
Kidney transplantationD01603011
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Acquired immunodeficiency syndromeD000163EFO_0000765B2022
Immunologic deficiency syndromesD007153D84.922
GlioblastomaD005909EFO_000051511
ViremiaD014766B34.911
Healthy volunteers/patients11
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Herpes zosterD006562EFO_0006510B0211
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
No data
Trends
No data
Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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250 adverse events reported
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