Sacrosidase
Sucraid (sacrosidase) is an enzyme pharmaceutical. Sacrosidase was first approved as Sucraid on 1998-04-09. It is used to treat congenital abnormalities and digestive system diseases in the USA.
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Commercial
Trade Name
FDA
EMA
Sucraid
Drug Products
FDA
EMA
Reference product - 351(a)
Reference product - 351(a)
Interchangeable product - 351(k)
Interchangeable product - 351(k)
Biosimilar product - 351(k)
Biosimilar product - 351(k)
Sacrosidase
Tradename | Proper name | Company | Number | Date | Products |
---|---|---|---|---|---|
Sucraid | sacrosidase | Qol Medical | N-20772 RX | 1998-04-09 | 2 products |
Labels
FDA
EMA
Brand Name | Status | Last Update |
---|---|---|
sucraid | Biologic Licensing Application | 2020-04-15 |
Indications
FDA
EMA
Indication | Ontology | MeSH | ICD-10 |
---|---|---|---|
congenital abnormalities | EFO_0003915 | D000013 | Q89.9 |
digestive system diseases | EFO_0000405 | D004066 | K92.9 |
Agency Specific
FDA
EMA
Expiration | Code | ||
---|---|---|---|
sacrosidase, Sucraid, QOL Medical, LLC | |||
2105-04-09 | Orphan excl. |
Patent Expiration
No data
HCPCS
No data
Clinical
Clinical Trials
62 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 |
---|---|---|---|---|---|---|---|---|---|
Neoplasms | D009369 | C80 | 10 | 6 | 1 | — | 1 | 15 | |
Ovarian neoplasms | D010051 | EFO_0003893 | C56 | 5 | 6 | 4 | — | — | 12 |
Fallopian tube neoplasms | D005185 | 3 | 5 | 5 | — | 1 | 12 | ||
Castration-resistant prostatic neoplasms | D064129 | 2 | 3 | 3 | — | — | 7 | ||
Prostatic neoplasms | D011471 | C61 | 2 | 4 | 1 | — | — | 6 | |
Ovarian epithelial carcinoma | D000077216 | — | 2 | 3 | — | 1 | 6 | ||
Peritoneal neoplasms | D010534 | 1 | 3 | 3 | — | — | 6 | ||
Adenocarcinoma | D000230 | — | 2 | 1 | — | — | 3 | ||
Large cell carcinoma | D018287 | — | — | 1 | — | — | 1 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Breast neoplasms | D001943 | EFO_0003869 | C50 | 3 | 3 | — | — | — | 6 |
Endometrial neoplasms | D016889 | EFO_0004230 | 1 | 4 | — | — | — | 4 | |
Small cell lung carcinoma | D055752 | 1 | 3 | — | — | — | 3 | ||
Pancreatic neoplasms | D010190 | EFO_0003860 | C25 | 1 | 3 | — | — | — | 3 |
Carcinosarcoma | D002296 | 1 | 1 | — | — | — | 2 | ||
Uterine cervical neoplasms | D002583 | — | 2 | — | — | — | 2 | ||
Biliary tract neoplasms | D001661 | C24.9 | 1 | 2 | — | — | — | 2 | |
Non-small-cell lung carcinoma | D002289 | 1 | 2 | — | — | — | 2 | ||
Urologic neoplasms | D014571 | C64-C68 | 1 | 2 | — | — | — | 2 | |
Malignant mesothelioma | D000086002 | — | 1 | — | — | — | 1 |
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Indications Phases 1
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Female genital neoplasms | D005833 | 1 | — | — | — | — | 1 |
Indications Without Phase
No data
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common name | SACROSIDASE |
INN | sacrosidase |
Description | Sacrosidase (trade name Sucraid) is a medication used to replace sucrase in people lacking this enzyme. It is available as an oral solution. Sucraid is approved by the U.S. Food and Drug Administration (FDA) for the therapy of the genetically determined sucrase deficiency that is part of the Congenital Sucrase-Isomaltase Deficiency (CSID). Sacrosidase assists in the breakdown of sugar/sucrose into simpler forms and is useful for the relief of gastrointestinal symptoms that are associated with CSID.
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Classification | Enzyme |
Drug class | enzymes |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | — |
Identifiers
PDB | — |
CAS-ID | 85897-35-4 |
RxCUI | 214817 |
ChEMBL ID | CHEMBL1201487 |
ChEBI ID | — |
PubChem CID | — |
DrugBank | DB06760 |
UNII ID | 8A7F670F2Y (ChemIDplus, GSRS) |
Target
Agency Approved
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Alternate
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Variants
Clinical Variant
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Financial
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Trends
PubMed Central
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Additional graphs summarizing 49 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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6,496 adverse events reported
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