Lucinactant
Surfaxin (lucinactant) is an unknown pharmaceutical. Lucinactant was first approved as Surfaxin on 2012-03-06.
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New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Lucinactant
Tradename | Company | Number | Date | Products |
---|---|---|---|---|
SURFAXIN | Windtree Therapeutics | N-021746 DISCN | 2012-03-06 | 1 products |
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Clinical
Clinical Trials
49 clinical trials
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Indications Phases 4
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Constipation | D003248 | HP_0002019 | K59.0 | 1 | 1 | 7 | 5 | 4 | 17 |
Healthy volunteers/patients | — | — | — | 1 | 1 | — | 2 | ||
Colonoscopy | D003113 | — | — | — | 2 | — | 2 | ||
Parkinson disease | D010300 | EFO_0002508 | G20 | — | — | — | 1 | 1 | 2 |
Multiple sclerosis | D009103 | EFO_0003885 | G35 | — | — | — | 1 | — | 1 |
Inflammatory bowel diseases | D015212 | EFO_0003767 | — | — | — | 1 | — | 1 |
Indications Phases 3
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Irritable bowel syndrome | D043183 | EFO_0000555 | K58 | 2 | 1 | 2 | — | 2 | 7 |
Opioid-induced constipation | D000079689 | — | — | 4 | — | 1 | 5 | ||
Colorectal neoplasms | D015179 | — | — | 1 | — | — | 1 | ||
Drug-related side effects and adverse reactions | D064420 | T88.7 | — | — | 1 | — | — | 1 | |
Treatment outcome | D016896 | — | — | 1 | — | — | 1 |
Indications Phases 1
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Indications Without Phase
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
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Cystic fibrosis | D003550 | EFO_0000390 | E84 | — | — | — | — | 1 | 1 |
Type 2 diabetes mellitus | D003924 | EFO_0001360 | E11 | — | — | — | — | 1 | 1 |
Type 1 diabetes mellitus | D003922 | EFO_0001359 | E10 | — | — | — | — | 1 | 1 |
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | LUCINACTANT |
INN | — |
Description | Lucinactant (trade name Surfaxin) is a liquid medication used to treat infant respiratory distress syndrome. It is a pulmonary surfactant for infants who lack enough natural surfactant in their lungs. Whereas earlier medicines of the class, such as beractant (Survanta & Beraksurf), calfactant (Infasurf), and poractant (Curosurf), are derived from animals, lucinactant is synthetic. It was approved for use in the United States by the U.S. Food and Drug Administration (FDA) on March 6, 2012.
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Classification | Small molecule |
Drug class | pulmonary surfactants; tachykinin (neurokinin) receptor antagonists |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
PDB | — |
CAS-ID | 825600-90-6 |
RxCUI | — |
ChEMBL ID | CHEMBL1963685 |
ChEBI ID | — |
PubChem CID | — |
DrugBank | DB04897 |
UNII ID | — |
Target
Agency Approved
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Additional graphs summarizing 225 documents
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Safety
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Adverse Events
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1,750 adverse events reported
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