Arimoclomol
Arimoclomol is a small molecule pharmaceutical. It is currently being investigated in clinical studies.
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Therapeutic Areas
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Trade Name
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Drug Products
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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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Labels
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Indications
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Agency Specific
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Patent Expiration
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HCPCS
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Clinical
Clinical Trials
11 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 |
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Amyotrophic lateral sclerosis | D000690 | EFO_0000253 | G12.21 | — | 3 | 3 | — | — | 5 |
Inclusion body myositis | D018979 | EFO_0007323 | G72.41 | — | 2 | 2 | — | — | 3 |
Type c niemann-pick disease | D052556 | Orphanet_646 | E75.242 | — | 1 | 1 | — | 1 | 2 |
Indications Phases 2
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
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Gaucher disease | D005776 | Orphanet_355 | E75.22 | — | 1 | — | — | — | 1 |
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 | ARIMOCLOMOL |
INN | arimoclomol |
Description | Arimoclomol (INN; originally codenamed BRX-345, which is a citrate salt formulation of BRX-220) is an experimental drug developed by CytRx Corporation, a biopharmaceutical company based in Los Angeles, California. In 2011 the worldwide rights to arimoclomol were bought by Danish biotech company Orphazyme ApS. The European Medicines Agency (EMA) and U.S. Food & Drug Administration (FDA) granted orphan drug designation to arimoclomol as a potential treatment for Niemann-Pick type C in 2014 and 2015 respectively.
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Classification | Small molecule |
Drug class | heat-shock protein inducers, bimoclomal type |
Image (chem structure or protein) | |
Structure (InChI/SMILES or Protein Sequence) | [O-][n+]1cccc(/C(Cl)=N/OC[C@H](O)CN2CCCCC2)c1 |
Identifiers
PDB | — |
CAS-ID | 289893-25-0 |
RxCUI | — |
ChEMBL ID | CHEMBL2107726 |
ChEBI ID | — |
PubChem CID | 208924 |
DrugBank | DB05025 |
UNII ID | EUT3557RT5 (ChemIDplus, GSRS) |
Target
Agency Approved
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Alternate
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Variants
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Trends
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Safety
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Adverse Events
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1 adverse events reported
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