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Drug ReportsHyperosmolar
Hyperosmolar
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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
26 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Type 2 diabetes mellitusD003924EFO_0001360E11112
HyperglycemiaD006943R73.9112
Diabetic ketoacidosisD016883EFO_1000897112
Brain edemaD001929EFO_1000845G93.6112
Insulin resistanceD007333EFO_0002614E88.81911
HypoglycemiaD007003E16.211
FastingD005215EFO_000275611
Hyperglycemic hyperosmolar nonketotic comaD00694411
Rotator cuff injuriesD000070636M75.111
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Traumatic brain injuriesD000070642S06213
Brain injuriesD001930S06.9213
Wounds and injuriesD014947T14.8213
Hemorrhagic shockD01277111
Indications Phases 2
No data
Indications Phases 1
No data
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Fuchs' endothelial dystrophyD005642EFO_0003946H18.5122
Cardiopulmonary bypassD00231522
Colorectal neoplasmsD01517911
Corneal edemaD015715EFO_1000879H18.2011
Diabetes insipidusD003919E23.211
NeuralgiaD009437EFO_000943011
Dry eye syndromesD015352H04.1211
HypertensionD006973EFO_0000537I1011
Intracranial hypertensionD019586EFO_100099211
Short bowel syndromeD012778K90.8211
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name
INN
Description
Classification
Unknown
Drug class
Image (chem structure or protein)Loading
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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1 adverse events reported
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