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Drug ReportsUrsodoxicoltaurine
Taurursodiol
Relyvrio (taurursodiol) is a small molecule pharmaceutical. Taurursodiol was first approved as Relyvrio on 2022-09-29. It is used to treat amyotrophic lateral sclerosis in the USA.
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FDA approval date
EMA approval date
Patent expiration date
Study first post date
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Results first post date
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
nervous system diseasesD009422
nutritional and metabolic diseasesD009750
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
No data
Labels
FDA
EMA
Brand Name
Status
Last Update
relyvrioNew Drug Application2024-01-02
Indications
FDA
EMA
No data
Agency Specific
FDA
EMA
Expiration
Code
SODIUM PHENYLBUTYRATE / TAURURSODIOL, RELYVRIO, AMYLYX
2029-09-29ODE-411
2027-09-29NCE
Patent Expiration
Patent
Expires
Flag
FDA Information
Sodium Phenylbutyrate / Taurursodiol, Relyvrio, Amylyx
115835422040-07-27DP
98728652033-12-24U-3460
102518962033-12-24U-3460
108571622033-12-24U-3460
110717422033-12-24DP
ATC Codes
No data
HCPCS
No data
Clinical
Clinical Trials
34 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
GallstonesD042882EFO_0004210————1—1
CholelithiasisD002769EFO_0004799K80———1—1
CholecystolithiasisD041761EFO_1000864————1—1
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Amyotrophic lateral sclerosisD000690HP_0007354G12.21—45—19
Motor neuron diseaseD016472EFO_0003782G12.2—45—19
SclerosisD012598——144—18
AmyloidosisD000686EFO_1001875E85121—14
Neurodegenerative diseasesD019636EFO_0005772G31.9—21——2
Liver cirrhosisD008103EFO_0001422K74.01—1——2
FibrosisD005355————1—12
CholestasisD002779HP_0001396K83.1——1—12
Biliary liver cirrhosisD008105—K74.3——1——1
Liver diseasesD008107HP_0002910K70-K77——1——1
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Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Diabetes mellitusD003920HP_0000819E08-E13—1——23
CardiomyopathiesD009202EFO_0000318I4211——12
Familial amyloid neuropathiesD028227—E85.1—1——12
Type 1 diabetes mellitusD003922EFO_0001359E10—1———1
Alzheimer diseaseD000544EFO_0000249F03—1———1
Central nervous system diseasesD002493HP_0002011G96.9—1———1
Nervous system diseasesD009422—G00-G99—1———1
Spinal cord diseasesD013118HP_0002196G95.9—1———1
Tdp-43 proteinopathiesD057177———1———1
Neuromuscular diseasesD009468EFO_1001902G70.9—1———1
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Vascular stiffnessD059289——1————1
VasodilationD014664——1————1
Huntington diseaseD006816Orphanet_399G101————1
Ulcerative colitisD003093EFO_0000729K511————1
ColitisD003092EFO_0003872K52.91————1
UlcerD014456MPATH_579—1————1
AsthmaD001249EFO_0000270J451————1
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Type 2 diabetes mellitusD003924EFO_0001360E11————22
Insulin resistanceD007333HP_0000855—————22
Disease progressionD018450——————11
Immunoglobulin light-chain amyloidosisD000075363——————11
Amyloid neuropathiesD017772——————11
Endoplasmic reticulum stressD059865EFO_1001886—————11
ObesityD009765EFO_0001073E66.9————11
Cystic fibrosisD003550EFO_0000390E84————11
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameTaurursodiol
INNursodoxicoltaurine
Description
Tauroursodeoxycholic acid is a bile acid taurine conjugate derived from ursoodeoxycholic acid. It has a role as a human metabolite, an anti-inflammatory agent, a neuroprotective agent, an apoptosis inhibitor, a cardioprotective agent and a bone density conservation agent. It is functionally related to an ursodeoxycholic acid. It is a conjugate acid of a tauroursodeoxycholate.
Classification
Small molecule
Drug class—
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Structure (InChI/SMILES or Protein Sequence)
C[C@H](CCC(=O)NCCS(=O)(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@@]21C
Identifiers
PDB—
CAS-ID14605-22-2
RxCUI—
ChEMBL IDCHEMBL272427
ChEBI ID80774
PubChem CID9848818
DrugBank—
UNII ID60EUX8MN5X (ChemIDplus, GSRS)
Target
No data
Variants
No data
Financial
No data
Trends
PubMed Central
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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598 adverse events reported
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