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Lucinactant
Surfaxin (lucinactant) is an unknown pharmaceutical. Lucinactant was first approved as Surfaxin on 2012-03-06.
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Commercial
Therapeutic Areas
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Trade Name
FDA
EMA
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Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Lucinactant
Tradename
Company
Number
Date
Products
SURFAXINWindtree TherapeuticsN-021746 DISCN2012-03-06
1 products
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Labels
FDA
EMA
No data
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
No data
HCPCS
No data
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
ConstipationD003248HP_0002019K59.01175417
Healthy volunteers/patients112
ColonoscopyD00311322
Parkinson diseaseD010300EFO_0002508G20112
Multiple sclerosisD009103EFO_0003885G3511
Inflammatory bowel diseasesD015212EFO_000376711
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Irritable bowel syndromeD043183EFO_0000555K5821227
Opioid-induced constipationD000079689415
Colorectal neoplasmsD01517911
Drug-related side effects and adverse reactionsD064420T88.711
Treatment outcomeD01689611
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
HivD006678O98.711
Indications Phases 1
No data
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Cystic fibrosisD003550EFO_0000390E8411
Type 2 diabetes mellitusD003924EFO_0001360E1111
Type 1 diabetes mellitusD003922EFO_0001359E1011
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameLUCINACTANT
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.
Classification
Small molecule
Drug classpulmonary surfactants; tachykinin (neurokinin) receptor antagonists
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
Identifiers
PDB
CAS-ID825600-90-6
RxCUI
ChEMBL IDCHEMBL1963685
ChEBI ID
PubChem CID
DrugBankDB04897
UNII ID
Target
Agency Approved
No data
Alternate
No data
Variants
Clinical Variant
No data
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 225 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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1,750 adverse events reported
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