Parnaparin sodium
Parnaparin sodium is an oligosaccharide pharmaceutical. It is currently being investigated in clinical studies.
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New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
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Indications
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ATC Codes
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Clinical
Clinical Trials
3 clinical trials
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Indications Phases 4
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Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
|---|---|---|---|---|---|---|---|---|---|
| Retinal vein occlusion | D012170 | EFO_1001157 | H34.81 | — | — | 1 | — | — | 1 |
| Infertility | D007246 | EFO_0000545 | — | — | 1 | — | — | 1 | |
| Thrombophlebitis | D013924 | HP_0004418 | — | — | 1 | — | — | 1 |
Indications Phases 2
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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 | PARNAPARIN SODIUM |
| INN | parnaparin sodium |
| Description | Parnaparin is an antithrombotic and belongs to the group of low molecular weight heparins. In the prevention and therapy of thromboembolic pathologies, the advent of this class of drugs represented a medical development, since they retain the same effectiveness of unfractionated heparin but with simpler dosing regimens and decreased side effects. In addition to being effective in treating proven deep vein thrombosis and thrombosis-associated phlebopathies, Parnaparin has demonstrated its thromboprophylactic efficacy in both high- and moderate-risk surgical patients.
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| Classification | Oligosaccharide |
| Drug class | heparin derivatives and low molecular weight (or depolymerized) heparins |
| Image (chem structure or protein) | |
| Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
| PDB | — |
| CAS-ID | 91449-79-5 |
| RxCUI | — |
| ChEMBL ID | CHEMBL2108080 |
| ChEBI ID | — |
| PubChem CID | — |
| DrugBank | DB09260 |
| UNII ID | U6K360XMIU (ChemIDplus, GSRS) |
Target
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Variants
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Safety
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Adverse Events
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2 adverse events reported
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