Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Multiple sclerosis | D009103 | EFO_0003885 | G35 | — | — | 1 | — | — | 1 |
Sclerosis | D012598 | — | — | — | — | 1 | — | — | 1 |
Indication | MeSH | Ontology | ICD-10 | Ph 1 | Ph 2 | Ph 3 | Ph 4 | Other | Total |
---|---|---|---|---|---|---|---|---|---|
Gastroesophageal reflux | D005764 | EFO_0003948 | K21 | — | 2 | — | — | — | 2 |
Peptic esophagitis | D004942 | EFO_1001095 | — | — | 1 | — | — | — | 1 |
Back pain | D001416 | — | M54 | — | 1 | — | — | — | 1 |
Spinal cord injuries | D013119 | EFO_1001919 | — | — | 1 | — | — | — | 1 |
Muscle spasticity | D009128 | — | — | — | 1 | — | — | — | 1 |
Drug common name | Arbaclofen placarbil |
INN | arbaclofen placarbil |
Description | Arbaclofen placarbil (/ɑːrˈbækloʊfɛn pləˈkɑːrbɪl/ ar-BAK-loh-fen plə-KAR-bil, also known as XP19986) is a prodrug of R-baclofen. Arbaclofen placarbil possesses more favorable pharmacokinetic profile than baclofen, with less fluctuations in plasma drug levels. It was being developed as a potential treatment for patients with GERD and spasticity due to multiple sclerosis; however, in May 2013 XenoPort announced the termination of development because of unsuccessful results in phase III clinical trials.
|
Classification | Small molecule |
Drug class | — |
Image (chem structure or protein) | ![]() |
Structure (InChI/SMILES or Protein Sequence) | CC(C)C(=O)O[C@@H](OC(=O)NC[C@H](CC(=O)O)c1ccc(Cl)cc1)C(C)C |
PDB | — |
CAS-ID | 847353-30-4 |
RxCUI | — |
ChEMBL ID | CHEMBL2107312 |
ChEBI ID | — |
PubChem CID | 11281011 |
DrugBank | — |
UNII ID | W89H91R7VX (ChemIDplus, GSRS) |